Canonical Allele Identifier: CA1499394775

Gene: IL15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733416T= , CM000666.2:g.141733416T=	GRCh38
NC_000004.11:g.142654569T= , CM000666.1:g.142654569T=	GRCh37
NC_000004.10:g.142874019T=	NCBI36
NG_029605.1:g.101821T=
NG_029605.2:g.101821T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*568T= MANE Select	ENSP00000323505.4:n.*568T=
ENST00000296545.11:c.*568T=	ENSP00000296545.7:n.*568T=
ENST00000320650.8:c.*568T=	ENSP00000323505.4:n.*568T=
ENST00000394159.2:c.976T=	ENSP00000377714.1:n.976T=
ENST00000477265.5:c.*568T=	ENSP00000436914.1:n.*568T=
NM_000585.4:c.*568T=	NP_000576.1:n.*568T=
NM_172175.2:c.*568T=	NP_751915.1:n.*568T=
NR_037840.2:n.1907T=
NM_000585.5:c.*568T= MANE Select	NP_000576.1:n.*568T=
NM_172175.3:c.*568T=	NP_751915.1:n.*568T=
NR_037840.3:n.1920T=