Canonical Allele Identifier: CA1499394427

Gene: IL15

Linked Data

• dbSNP Id: rs1730503061
• gnomAD v4: 4-141732995-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732996_141732997del , CM000666.2:g.141732996_141732997del	GRCh38
NC_000004.11:g.142654149_142654150del , CM000666.1:g.142654149_142654150del	GRCh37
NC_000004.10:g.142873599_142873600del	NCBI36
NG_029605.1:g.101401_101402del
NG_029605.2:g.101401_101402del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*148_*149del MANE Select	ENSP00000323505.4:n.*148_*149del
ENST00000296545.11:c.*148_*149del	ENSP00000296545.7:n.*148_*149del
ENST00000320650.8:c.*148_*149del	ENSP00000323505.4:n.*148_*149del
ENST00000394159.2:c.556_557del	ENSP00000377714.1:n.556_557del
ENST00000477265.5:c.*148_*149del	ENSP00000436914.1:n.*148_*149del
ENST00000514653.5:c.*148_*149del	ENSP00000422271.1:n.*148_*149del
ENST00000529613.5:c.*148_*149del	ENSP00000435462.1:n.*148_*149del
NM_000585.4:c.*148_*149del	NP_000576.1:n.*148_*149del
NM_172175.2:c.*148_*149del	NP_751915.1:n.*148_*149del
NR_037840.2:n.1487_1488del
NM_000585.5:c.*148_*149del MANE Select	NP_000576.1:n.*148_*149del
NM_172175.3:c.*148_*149del	NP_751915.1:n.*148_*149del
NR_037840.3:n.1500_1501del