Canonical Allele Identifier: CA917320862

Gene: IL15

Linked Data

• dbSNP Id: rs1579062090
• gnomAD v4: 4-141733054-GACTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733059_141733062del , CM000666.2:g.141733059_141733062del	GRCh38
NC_000004.11:g.142654212_142654215del , CM000666.1:g.142654212_142654215del	GRCh37
NC_000004.10:g.142873662_142873665del	NCBI36
NG_029605.1:g.101464_101467del
NG_029605.2:g.101464_101467del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*211_*214del MANE Select	ENSP00000323505.4:n.*211_*214del
ENST00000296545.11:c.*211_*214del	ENSP00000296545.7:n.*211_*214del
ENST00000320650.8:c.*211_*214del	ENSP00000323505.4:n.*211_*214del
ENST00000394159.2:c.619_622del	ENSP00000377714.1:n.619_622del
ENST00000477265.5:c.*211_*214del	ENSP00000436914.1:n.*211_*214del
ENST00000514653.5:c.*211_*214del	ENSP00000422271.1:n.*211_*214del
ENST00000529613.5:c.*211_*214del	ENSP00000435462.1:n.*211_*214del
NM_000585.4:c.*211_*214del	NP_000576.1:n.*211_*214del
NM_172175.2:c.*211_*214del	NP_751915.1:n.*211_*214del
NR_037840.2:n.1550_1553del
NM_000585.5:c.*211_*214del MANE Select	NP_000576.1:n.*211_*214del
NM_172175.3:c.*211_*214del	NP_751915.1:n.*211_*214del
NR_037840.3:n.1563_1566del