Canonical Allele Identifier: CA2672190059

Gene: IL15

Linked Data

• gnomAD v4: 4-141733000-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733000A>G , CM000666.2:g.141733000A>G	GRCh38
NC_000004.11:g.142654153A>G , CM000666.1:g.142654153A>G	GRCh37
NC_000004.10:g.142873603A>G	NCBI36
NG_029605.1:g.101405A>G
NG_029605.2:g.101405A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*152A>G MANE Select	ENSP00000323505.4:n.*152A>G
ENST00000296545.11:c.*152A>G	ENSP00000296545.7:n.*152A>G
ENST00000320650.8:c.*152A>G	ENSP00000323505.4:n.*152A>G
ENST00000394159.2:c.560A>G	ENSP00000377714.1:n.560A>G
ENST00000477265.5:c.*152A>G	ENSP00000436914.1:n.*152A>G
ENST00000514653.5:c.*152A>G	ENSP00000422271.1:n.*152A>G
ENST00000529613.5:c.*152A>G	ENSP00000435462.1:n.*152A>G
NM_000585.4:c.*152A>G	NP_000576.1:n.*152A>G
NM_172175.2:c.*152A>G	NP_751915.1:n.*152A>G
NR_037840.2:n.1491A>G
NM_000585.5:c.*152A>G MANE Select	NP_000576.1:n.*152A>G
NM_172175.3:c.*152A>G	NP_751915.1:n.*152A>G
NR_037840.3:n.1504A>G