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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_029605.2 RefSeqGene
- Range
-
4988..102392
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_000585.5 → NP_000576.1 interleukin-15 isoform 1 preproprotein
See identical proteins and their annotated locations for NP_000576.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) represents the shortest transcript and encodes the longer isoform (1, also known as 48aa(LSP)-IL15).
- Source sequence(s)
-
AA897685, AC096774, AC118480, BX116580, CX761071
- Consensus CDS
-
CCDS3755.1
- UniProtKB/Swiss-Prot
- D3DNZ2, O00440, O43512, P40933, Q495Z8, Q6FGX7, Q93058, Q9UBA3
- Related
- ENSP00000323505.4, ENST00000320650.9
- Conserved Domains (1) summary
-
- pfam02372
Location:33 → 154
- IL15; Interleukin 15
-
NM_172175.3 → NP_751915.1 interleukin-15 isoform 2 preproprotein
See identical proteins and their annotated locations for NP_751915.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) differs in the 5' UTR and contains an alternate exon in the 5' coding region. This variant uses an alternate downstream start codon, compared to variant 1. Isoform 2 (also known as (21aa(SSP)-IL15) has a shorter and distinct N-terminus, compared to isoform 1.
- Source sequence(s)
-
AA897685, AC096774, AC118480, AK290619, BX116580, CX761071
- Consensus CDS
-
CCDS3756.1
- UniProtKB/Swiss-Prot
-
P40933
- Related
- ENSP00000422271.1, ENST00000514653.5
- Conserved Domains (1) summary
-
- pfam02372
Location:10 → 127
- IL15; Interleukin 15
RNA
-
NR_037840.3 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) has an alternate 5' exon, compared to variant 3. This variant is represented as non-coding due to the presence of an upstream ORF that is predicted to interfere with translation of the longest ORF; translation of the upstream ORF renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AA897685, AC096774, AC118480, BC018149, CX761071
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_000004.12 Reference GRCh38.p14 Primary Assembly
- Range
-
141636583..141733987
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060928.1 Alternate T2T-CHM13v2.0
- Range
-
144953939..145051309
- 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.
-
NM_172174.2: Suppressed sequence
- Description
- NM_172174.2: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.