Canonical Allele Identifier: CA1499394408

Gene: IL15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732961_141732964delinsCAAG , CM000666.2:g.141732961_141732964delinsCAAG	GRCh38
NC_000004.11:g.142654114_142654117delinsCAAG , CM000666.1:g.142654114_142654117delinsCAAG	GRCh37
NC_000004.10:g.142873564_142873567delinsCAAG	NCBI36
NG_029605.1:g.101366_101369delinsCAAG
NG_029605.2:g.101366_101369delinsCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*113_*116delinsCAAG MANE Select	ENSP00000323505.4:n.*113_*116delinsCAAG
ENST00000296545.11:c.*113_*116delinsCAAG	ENSP00000296545.7:n.*113_*116delinsCAAG
ENST00000320650.8:c.*113_*116delinsCAAG	ENSP00000323505.4:n.*113_*116delinsCAAG
ENST00000394159.2:c.521_524delinsCAAG	ENSP00000377714.1:n.521_524delinsCAAG
ENST00000477265.5:c.*113_*116delinsCAAG	ENSP00000436914.1:n.*113_*116delinsCAAG
ENST00000514653.5:c.*113_*116delinsCAAG	ENSP00000422271.1:n.*113_*116delinsCAAG
ENST00000529613.5:c.*113_*116delinsCAAG	ENSP00000435462.1:n.*113_*116delinsCAAG
NM_000585.4:c.*113_*116delinsCAAG	NP_000576.1:n.*113_*116delinsCAAG
NM_172175.2:c.*113_*116delinsCAAG	NP_751915.1:n.*113_*116delinsCAAG
NR_037840.2:n.1452_1455delinsCAAG
NM_000585.5:c.*113_*116delinsCAAG MANE Select	NP_000576.1:n.*113_*116delinsCAAG
NM_172175.3:c.*113_*116delinsCAAG	NP_751915.1:n.*113_*116delinsCAAG
NR_037840.3:n.1465_1468delinsCAAG