Canonical Allele Identifier: CA1499394426

Gene: IL15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732995_141732997delinsCTT , CM000666.2:g.141732995_141732997delinsCTT	GRCh38
NC_000004.11:g.142654148_142654150delinsCTT , CM000666.1:g.142654148_142654150delinsCTT	GRCh37
NC_000004.10:g.142873598_142873600delinsCTT	NCBI36
NG_029605.1:g.101400_101402delinsCTT
NG_029605.2:g.101400_101402delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*147_*149delinsCTT MANE Select	ENSP00000323505.4:n.*147_*149delinsCTT
ENST00000296545.11:c.*147_*149delinsCTT	ENSP00000296545.7:n.*147_*149delinsCTT
ENST00000320650.8:c.*147_*149delinsCTT	ENSP00000323505.4:n.*147_*149delinsCTT
ENST00000394159.2:c.555_557delinsCTT	ENSP00000377714.1:n.555_557delinsCTT
ENST00000477265.5:c.*147_*149delinsCTT	ENSP00000436914.1:n.*147_*149delinsCTT
ENST00000514653.5:c.*147_*149delinsCTT	ENSP00000422271.1:n.*147_*149delinsCTT
ENST00000529613.5:c.*147_*149delinsCTT	ENSP00000435462.1:n.*147_*149delinsCTT
NM_000585.4:c.*147_*149delinsCTT	NP_000576.1:n.*147_*149delinsCTT
NM_172175.2:c.*147_*149delinsCTT	NP_751915.1:n.*147_*149delinsCTT
NR_037840.2:n.1486_1488delinsCTT
NM_000585.5:c.*147_*149delinsCTT MANE Select	NP_000576.1:n.*147_*149delinsCTT
NM_172175.3:c.*147_*149delinsCTT	NP_751915.1:n.*147_*149delinsCTT
NR_037840.3:n.1499_1501delinsCTT