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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.
mRNA and Protein(s)
-
NM_001290117.2 → NP_001277046.1 mitochondrial import inner membrane translocase subunit Tim23B isoform 1
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longer isoform (1).
- Source sequence(s)
-
AK098044, AK293228, AL542628, BU620107, BU928648, DC419977
- Consensus CDS
-
CCDS73131.1
- UniProtKB/Swiss-Prot
- B4DDK6, E7EP42, Q5SRD1, Q5SRD2
- UniProtKB/TrEMBL
-
B4DI18
- Related
- ENSP00000502369.1, ENST00000651259.3
- Conserved Domains (1) summary
-
- cl02381
Location:46 → 171
- Tim17; Tim17/Tim22/Tim23/Pmp24 family
-
NM_001290118.2 → NP_001277047.1 mitochondrial import inner membrane translocase subunit Tim23B isoform 2
See identical proteins and their annotated locations for NP_001277047.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) lacks two exons in the coding region, compared to variant 1, which results in a shorter protein (isoform 2), compared to isoform 1.
- Source sequence(s)
-
AK098044, AK293228, BU620107, BU928648, DA019889, DC419977
- Consensus CDS
-
CCDS76301.1
- UniProtKB/TrEMBL
-
B4DDK6
- Related
- ENSP00000502146.1, ENST00000652716.1
- Conserved Domains (1) summary
-
- cl02381
Location:46 → 123
- Tim17; Tim17/Tim22/Tim23/Pmp24 family
-
NM_001365871.1 → NP_001352800.1 mitochondrial import inner membrane translocase subunit Tim23B isoform 3
Status: VALIDATED
- Source sequence(s)
-
AL442003, FO393433, FP565721
- Conserved Domains (1) summary
-
- cl02381
Location:1 → 87
- Tim17; Tim17/Tim22/Tim23/Pmp24 family
RNA
-
NR_110767.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) contains an alternate exon, compared to variant 1. This variant is represented as non-coding because the use of the expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AK098044, AK293228, AL542628, BU620107, BU928648, DC419977
- Related
-
ENST00000478381.5
-
NR_158651.1 RNA Sequence
Status: VALIDATED
- Source sequence(s)
-
AL442003, FO393433, FP565721
-
NR_158652.1 RNA Sequence
Status: VALIDATED
- Source sequence(s)
-
AL442003, FO393433, FP565721
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_000010.11 Reference GRCh38.p14 Primary Assembly
- Range
-
49942053..49974850
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060934.1 Alternate T2T-CHM13v2.0
- Range
-
50791695..50824486
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the
cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related
sequence links, or BLAST links (BLink), but may still be retrieved by clicking on
their accession.version below.
-
NR_135475.1: Suppressed sequence
- Description
- NR_135475.1: This RefSeq has been removed because it is thought to be partial.