Canonical Allele Identifier: CA358388176

Gene: IL15

Linked Data

• MyVariant Identifiers: chr4:g.142653996T>A (hg19) ; chr4:g.141732843T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732843T>A , CM000666.2:g.141732843T>A	GRCh38
NC_000004.11:g.142653996T>A , CM000666.1:g.142653996T>A	GRCh37
NC_000004.10:g.142873446T>A	NCBI36
NG_029605.1:g.101248T>A
NG_029605.2:g.101248T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000320650.9:c.484T>A MANE Select	ENSP00000323505.4:p.Ser162Thr
ENST00000296545.11:c.484T>A	ENSP00000296545.7:p.Ser162Thr
ENST00000320650.8:c.484T>A	ENSP00000323505.4:p.Ser162Thr
ENST00000394159.2:c.403T>A	ENSP00000377714.1:p.Ser135Thr
ENST00000477265.5:c.403T>A	ENSP00000436914.1:p.Ser135Thr
ENST00000514653.5:c.403T>A	ENSP00000422271.1:p.Ser135Thr
ENST00000529613.5:c.484T>A	ENSP00000435462.1:p.Ser162Thr
NM_000585.4:c.484T>A	NP_000576.1:p.Ser162Thr
NM_172175.2:c.403T>A	NP_751915.1:p.Ser135Thr
NR_037840.2:n.1334T>A
NM_000585.5:c.484T>A MANE Select	NP_000576.1:p.Ser162Thr
NM_172175.3:c.403T>A	NP_751915.1:p.Ser135Thr
NR_037840.3:n.1347T>A