Canonical Allele Identifier: CA788189094
Gene: IL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141719385T>A , CM000666.2:g.141719385T>A GRCh38
NC_000004.11:g.142640538T>A , CM000666.1:g.142640538T>A GRCh37
NC_000004.10:g.142859988T>A NCBI36
NG_029605.1:g.87790T>A
NG_029605.2:g.87790T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.-80T>A MANE Select ENSP00000323505.4:n.-80T>A
ENST00000296545.11:c.-80T>A ENSP00000296545.7:n.-80T>A
ENST00000320650.8:c.-80T>A ENSP00000323505.4:n.-80T>A
ENST00000477265.5:c.-280T>A ENSP00000436914.1:n.-280T>A
ENST00000505351.1:n.255T>A
ENST00000514653.5:c.-280T>A ENSP00000422271.1:n.-280T>A
ENST00000529613.5:c.-80T>A ENSP00000435462.1:n.-80T>A
NM_000585.4:c.-80T>A NP_000576.1:n.-80T>A
NM_172175.2:c.-280T>A NP_751915.1:n.-280T>A
NR_037840.2:n.771T>A
NM_000585.5:c.-80T>A MANE Select NP_000576.1:n.-80T>A
NM_172175.3:c.-280T>A NP_751915.1:n.-280T>A
NR_037840.3:n.784T>A