Canonical Allele Identifier: CA1499394488

Gene: IL15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733068_141733069delinsAT , CM000666.2:g.141733068_141733069delinsAT	GRCh38
NC_000004.11:g.142654221_142654222delinsAT , CM000666.1:g.142654221_142654222delinsAT	GRCh37
NC_000004.10:g.142873671_142873672delinsAT	NCBI36
NG_029605.1:g.101473_101474delinsAT
NG_029605.2:g.101473_101474delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*220_*221delinsAT MANE Select	ENSP00000323505.4:n.*220_*221delinsAT
ENST00000296545.11:c.*220_*221delinsAT	ENSP00000296545.7:n.*220_*221delinsAT
ENST00000320650.8:c.*220_*221delinsAT	ENSP00000323505.4:n.*220_*221delinsAT
ENST00000394159.2:c.628_629delinsAT	ENSP00000377714.1:n.628_629delinsAT
ENST00000477265.5:c.*220_*221delinsAT	ENSP00000436914.1:n.*220_*221delinsAT
ENST00000514653.5:c.*220_*221delinsAT	ENSP00000422271.1:n.*220_*221delinsAT
ENST00000529613.5:c.*220_*221delinsAT	ENSP00000435462.1:n.*220_*221delinsAT
NM_000585.4:c.*220_*221delinsAT	NP_000576.1:n.*220_*221delinsAT
NM_172175.2:c.*220_*221delinsAT	NP_751915.1:n.*220_*221delinsAT
NR_037840.2:n.1559_1560delinsAT
NM_000585.5:c.*220_*221delinsAT MANE Select	NP_000576.1:n.*220_*221delinsAT
NM_172175.3:c.*220_*221delinsAT	NP_751915.1:n.*220_*221delinsAT
NR_037840.3:n.1572_1573delinsAT