Canonical Allele Identifier: CA2672190198

Gene: IL15

Linked Data

• gnomAD v4: 4-141733238-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733238C>T , CM000666.2:g.141733238C>T	GRCh38
NC_000004.11:g.142654391C>T , CM000666.1:g.142654391C>T	GRCh37
NC_000004.10:g.142873841C>T	NCBI36
NG_029605.1:g.101643C>T
NG_029605.2:g.101643C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*390C>T MANE Select	ENSP00000323505.4:n.*390C>T
ENST00000296545.11:c.*390C>T	ENSP00000296545.7:n.*390C>T
ENST00000320650.8:c.*390C>T	ENSP00000323505.4:n.*390C>T
ENST00000394159.2:c.798C>T	ENSP00000377714.1:n.798C>T
ENST00000477265.5:c.*390C>T	ENSP00000436914.1:n.*390C>T
NM_000585.4:c.*390C>T	NP_000576.1:n.*390C>T
NM_172175.2:c.*390C>T	NP_751915.1:n.*390C>T
NR_037840.2:n.1729C>T
NM_000585.5:c.*390C>T MANE Select	NP_000576.1:n.*390C>T
NM_172175.3:c.*390C>T	NP_751915.1:n.*390C>T
NR_037840.3:n.1742C>T