Canonical Allele Identifier: CA2672190109

Gene: IL15

Linked Data

• gnomAD v4: 4-141733065-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733065C>A , CM000666.2:g.141733065C>A	GRCh38
NC_000004.11:g.142654218C>A , CM000666.1:g.142654218C>A	GRCh37
NC_000004.10:g.142873668C>A	NCBI36
NG_029605.1:g.101470C>A
NG_029605.2:g.101470C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*217C>A MANE Select	ENSP00000323505.4:n.*217C>A
ENST00000296545.11:c.*217C>A	ENSP00000296545.7:n.*217C>A
ENST00000320650.8:c.*217C>A	ENSP00000323505.4:n.*217C>A
ENST00000394159.2:c.625C>A	ENSP00000377714.1:n.625C>A
ENST00000477265.5:c.*217C>A	ENSP00000436914.1:n.*217C>A
ENST00000514653.5:c.*217C>A	ENSP00000422271.1:n.*217C>A
ENST00000529613.5:c.*217C>A	ENSP00000435462.1:n.*217C>A
NM_000585.4:c.*217C>A	NP_000576.1:n.*217C>A
NM_172175.2:c.*217C>A	NP_751915.1:n.*217C>A
NR_037840.2:n.1556C>A
NM_000585.5:c.*217C>A MANE Select	NP_000576.1:n.*217C>A
NM_172175.3:c.*217C>A	NP_751915.1:n.*217C>A
NR_037840.3:n.1569C>A