NEW
Try the new Transcript table
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_001277783.2 → NP_001264712.1 ubiquitin-like protein ATG12 isoform 2
See identical proteins and their annotated locations for NP_001264712.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (5) lacks an exon in the coding region compared to variant 1. The resulting protein (isoform 2) is shorter and has a distinct C-terminus compared to isoform 1.
- Source sequence(s)
-
AC026449, BC011033
- Consensus CDS
-
CCDS64222.1
- UniProtKB/Swiss-Prot
-
O94817
- Related
- ENSP00000425164.1, ENST00000500945.2
-
NM_004707.4 → NP_004698.3 ubiquitin-like protein ATG12 isoform 1
See identical proteins and their annotated locations for NP_004698.3
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longer protein (isoform 1).
- Source sequence(s)
-
AC026449, BC012266, DB530852
- Consensus CDS
-
CCDS4122.2
- UniProtKB/Swiss-Prot
- O94817, Q6PJV2
- UniProtKB/TrEMBL
-
B2R8C8
- Related
- ENSP00000425107.1, ENST00000509910.2
- Conserved Domains (1) summary
-
- pfam04110
Location:54 → 140
- APG12; Ubiquitin-like autophagy protein Apg12
RNA
-
NR_033362.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) includes an additional internal exon in the 5' region, compared to variant 1. This variant is represented as non-coding because the use of the supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AC026449, CN400030, DA005347, DB530852
-
NR_033363.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) includes an additional internal exon in the 5' region, compared to variant 1. This variant is represented as non-coding because the use of the supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AC026449, CB995198, DA005347, DB530852
-
NR_073603.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) contains two alternate exons compared to variant 1. This variant is represented as non-coding because the use of the supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AC026449, AK313320
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_000005.10 Reference GRCh38.p14 Primary Assembly
- Range
-
115828200..115841565 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060929.1 Alternate T2T-CHM13v2.0
- Range
-
116340597..116353961 complement
- 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_073604.1: Suppressed sequence
- Description
- NR_073604.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript.