Canonical Allele Identifier: CA2672190137

Gene: IL15

Linked Data

• gnomAD v4: 4-141733114-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733114T>A , CM000666.2:g.141733114T>A	GRCh38
NC_000004.11:g.142654267T>A , CM000666.1:g.142654267T>A	GRCh37
NC_000004.10:g.142873717T>A	NCBI36
NG_029605.1:g.101519T>A
NG_029605.2:g.101519T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*266T>A MANE Select	ENSP00000323505.4:n.*266T>A
ENST00000296545.11:c.*266T>A	ENSP00000296545.7:n.*266T>A
ENST00000320650.8:c.*266T>A	ENSP00000323505.4:n.*266T>A
ENST00000394159.2:c.674T>A	ENSP00000377714.1:n.674T>A
ENST00000477265.5:c.*266T>A	ENSP00000436914.1:n.*266T>A
ENST00000514653.5:c.*266T>A	ENSP00000422271.1:n.*266T>A
ENST00000529613.5:c.*266T>A	ENSP00000435462.1:n.*266T>A
NM_000585.4:c.*266T>A	NP_000576.1:n.*266T>A
NM_172175.2:c.*266T>A	NP_751915.1:n.*266T>A
NR_037840.2:n.1605T>A
NM_000585.5:c.*266T>A MANE Select	NP_000576.1:n.*266T>A
NM_172175.3:c.*266T>A	NP_751915.1:n.*266T>A
NR_037840.3:n.1618T>A