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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
Genomic
-
NG_023231.1 RefSeqGene
- Range
-
5360..29255
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001139441.1 → NP_001132913.1 B-cell receptor-associated protein 31 isoform b
See identical proteins and their annotated locations for NP_001132913.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) differs in the 5' UTR, lacks a portion of the 5' coding region, and uses a downstream in-frame start codon, compared to variant 1. The encoded isoform (b) is shorter at the N-terminus, compared to isoform a. Variants 2, 3 and 4 all encode isoform b.
- Source sequence(s)
-
AI123868, BC065292, CX164660, DA819112
- Consensus CDS
-
CCDS14727.1
- UniProtKB/Swiss-Prot
- B3KQ79, D3DWV5, P51572, Q13836, Q96CF0
- UniProtKB/TrEMBL
- Q53G72, Q53HT6
- Conserved Domains (3) summary
-
- PRK02224
Location:134 → 229
- PRK02224; DNA double-strand break repair Rad50 ATPase
- pfam05529
Location:1 → 136
- Bap31; B-cell receptor-associated protein 31-like
- pfam18035
Location:193 → 246
- Bap31_Bap29_C; Bap31/Bap29 cytoplasmic coiled-coil domain
-
NM_001139457.2 → NP_001132929.1 B-cell receptor-associated protein 31 isoform a
See identical proteins and their annotated locations for NP_001132929.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) represents the longest transcript and encodes the longer isoform (a).
- Source sequence(s)
-
AI123868, AK057613, BG779815
- Consensus CDS
-
CCDS48191.1
- UniProtKB/Swiss-Prot
-
P51572
- Related
- ENSP00000392330.2, ENST00000458587.8
- Conserved Domains (1) summary
-
- pfam05529
Location:68 → 291
- Bap31; B-cell receptor-associated protein 31-like
-
NM_001256447.2 → NP_001243376.1 B-cell receptor-associated protein 31 isoform b
See identical proteins and their annotated locations for NP_001243376.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (4) differs in the 5' UTR, lacks a portion of the 5' coding region, and uses a downstream in-frame start codon, compared to variant 1. The encoded isoform (b) is shorter at the N-terminus, compared to isoform a. Variants 2, 3 and 4 all encode isoform b.
- Source sequence(s)
-
AI123868, BC065292, DA134013, U52111
- Consensus CDS
-
CCDS14727.1
- UniProtKB/Swiss-Prot
- B3KQ79, D3DWV5, P51572, Q13836, Q96CF0
- UniProtKB/TrEMBL
- Q53G72, Q53HT6
- Related
- ENSP00000343458.6, ENST00000345046.12
- Conserved Domains (3) summary
-
- PRK02224
Location:134 → 229
- PRK02224; DNA double-strand break repair Rad50 ATPase
- pfam05529
Location:1 → 136
- Bap31; B-cell receptor-associated protein 31-like
- pfam18035
Location:193 → 246
- Bap31_Bap29_C; Bap31/Bap29 cytoplasmic coiled-coil domain
-
NM_005745.8 → NP_005736.3 B-cell receptor-associated protein 31 isoform b
See identical proteins and their annotated locations for NP_005736.3
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) differs in the 5' UTR, lacks a portion of the 5' coding region, and uses a downstream in-frame start codon, compared to variant 1. The encoded isoform (b) is shorter at the N-terminus, compared to isoform a. Variants 2, 3 and 4 all encode isoform b.
- Source sequence(s)
-
AI123868, AU132745, BC065292, BX474419, U52111
- Consensus CDS
-
CCDS14727.1
- UniProtKB/Swiss-Prot
- B3KQ79, D3DWV5, P51572, Q13836, Q96CF0
- UniProtKB/TrEMBL
- Q53G72, Q53HT6
- Related
- ENSP00000499882.1, ENST00000672675.1
- Conserved Domains (3) summary
-
- PRK02224
Location:134 → 229
- PRK02224; DNA double-strand break repair Rad50 ATPase
- pfam05529
Location:1 → 136
- Bap31; B-cell receptor-associated protein 31-like
- pfam18035
Location:193 → 246
- Bap31_Bap29_C; Bap31/Bap29 cytoplasmic coiled-coil domain
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000023.11 Reference GRCh38.p14 Primary Assembly
- Range
-
153700492..153724387 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060947.1 Alternate T2T-CHM13v2.0
- Range
-
151974158..151998050 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)