Canonical Allele Identifier: CA1499382146

Gene: IL15

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141719484A>C , CM000666.2:g.141719484A>C	GRCh38
NC_000004.11:g.142640637A>C , CM000666.1:g.142640637A>C	GRCh37
NC_000004.10:g.142860087A>C	NCBI36
NG_029605.1:g.87889A>C
NG_029605.2:g.87889A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.12+8A>C MANE Select	ENSP00000323505.4:n.12+8A>C
ENST00000296545.11:c.12+8A>C	ENSP00000296545.7:n.12+8A>C
ENST00000320650.8:c.12+8A>C	ENSP00000323505.4:n.12+8A>C
ENST00000477265.5:c.-189+8A>C	ENSP00000436914.1:n.-189+8A>C
ENST00000505351.1:n.346+8A>C
ENST00000514653.5:c.-189+8A>C	ENSP00000422271.1:n.-189+8A>C
ENST00000529613.5:c.12+8A>C	ENSP00000435462.1:n.12+8A>C
NM_000585.4:c.12+8A>C	NP_000576.1:n.12+8A>C
NM_172175.2:c.-189+8A>C	NP_751915.1:n.-189+8A>C
NR_037840.2:n.862+8A>C
NM_000585.5:c.12+8A>C MANE Select	NP_000576.1:n.12+8A>C
NM_172175.3:c.-189+8A>C	NP_751915.1:n.-189+8A>C
NR_037840.3:n.875+8A>C