Canonical Allele Identifier: CA1499394474

Gene: IL15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733040A= , CM000666.2:g.141733040A=	GRCh38
NC_000004.11:g.142654193A= , CM000666.1:g.142654193A=	GRCh37
NC_000004.10:g.142873643A=	NCBI36
NG_029605.1:g.101445A=
NG_029605.2:g.101445A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*192A= MANE Select	ENSP00000323505.4:n.*192A=
ENST00000296545.11:c.*192A=	ENSP00000296545.7:n.*192A=
ENST00000320650.8:c.*192A=	ENSP00000323505.4:n.*192A=
ENST00000394159.2:c.600A=	ENSP00000377714.1:n.600A=
ENST00000477265.5:c.*192A=	ENSP00000436914.1:n.*192A=
ENST00000514653.5:c.*192A=	ENSP00000422271.1:n.*192A=
ENST00000529613.5:c.*192A=	ENSP00000435462.1:n.*192A=
NM_000585.4:c.*192A=	NP_000576.1:n.*192A=
NM_172175.2:c.*192A=	NP_751915.1:n.*192A=
NR_037840.2:n.1531A=
NM_000585.5:c.*192A= MANE Select	NP_000576.1:n.*192A=
NM_172175.3:c.*192A=	NP_751915.1:n.*192A=
NR_037840.3:n.1544A=