Canonical Allele Identifier: CA1499360983

Gene: IL15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141644540T= , CM000666.2:g.141644540T=	GRCh38
NC_000004.11:g.142565693T= , CM000666.1:g.142565693T=	GRCh37
NC_000004.10:g.142785143T=	NCBI36
NG_029605.1:g.12945T=
NG_029605.2:g.12945T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000585.5:c.-222+7792T= MANE Select	NP_000576.1:n.-222+7792T=
ENST00000320650.9:c.-222+7792T= MANE Select	ENSP00000323505.4:n.-222+7792T=
NM_000585.4:c.-222+7792T=	NP_000576.1:n.-222+7792T=
NM_172175.2:c.-624+7792T=	NP_751915.1:n.-624+7792T=
NM_172175.3:c.-624+7792T=	NP_751915.1:n.-624+7792T=
NR_037840.2:n.629+7316T=
NR_037840.3:n.642+7316T=
ENST00000296545.11:c.-222+7316T=	ENSP00000296545.7:n.-222+7316T=
ENST00000320650.8:c.-222+7792T=	ENSP00000323505.4:n.-222+7792T=
ENST00000514653.5:c.-624+7792T=	ENSP00000422271.1:n.-624+7792T=
ENST00000529613.5:c.-314+7316T=	ENSP00000435462.1:n.-314+7316T=