Canonical Allele Identifier: CA1499394404
Gene: IL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141732958T= , CM000666.2:g.141732958T= GRCh38
NC_000004.11:g.142654111T= , CM000666.1:g.142654111T= GRCh37
NC_000004.10:g.142873561T= NCBI36
NG_029605.1:g.101363T=
NG_029605.2:g.101363T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*110T= MANE Select ENSP00000323505.4:n.*110T=
ENST00000296545.11:c.*110T= ENSP00000296545.7:n.*110T=
ENST00000320650.8:c.*110T= ENSP00000323505.4:n.*110T=
ENST00000394159.2:c.518T= ENSP00000377714.1:n.518T=
ENST00000477265.5:c.*110T= ENSP00000436914.1:n.*110T=
ENST00000514653.5:c.*110T= ENSP00000422271.1:n.*110T=
ENST00000529613.5:c.*110T= ENSP00000435462.1:n.*110T=
NM_000585.4:c.*110T= NP_000576.1:n.*110T=
NM_172175.2:c.*110T= NP_751915.1:n.*110T=
NR_037840.2:n.1449T=
NM_000585.5:c.*110T= MANE Select NP_000576.1:n.*110T=
NM_172175.3:c.*110T= NP_751915.1:n.*110T=
NR_037840.3:n.1462T=