Canonical Allele Identifier: CA2672190359

Gene: IL15

Linked Data

• gnomAD v4: 4-141733401-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733404del , CM000666.2:g.141733404del	GRCh38
NC_000004.11:g.142654557del , CM000666.1:g.142654557del	GRCh37
NC_000004.10:g.142874007del	NCBI36
NG_029605.1:g.101809del
NG_029605.2:g.101809del

Transcript Alleles

HGVS	Amino-acid change
ENST00000320650.9:c.*556del MANE Select	ENSP00000323505.4:n.*556del
ENST00000296545.11:c.*556del	ENSP00000296545.7:n.*556del
ENST00000320650.8:c.*556del	ENSP00000323505.4:n.*556del
ENST00000394159.2:c.964del	ENSP00000377714.1:n.964del
ENST00000477265.5:c.*556del	ENSP00000436914.1:n.*556del
NM_000585.4:c.*556del	NP_000576.1:n.*556del
NM_172175.2:c.*556del	NP_751915.1:n.*556del
NR_037840.2:n.1895del
NM_000585.5:c.*556del MANE Select	NP_000576.1:n.*556del
NM_172175.3:c.*556del	NP_751915.1:n.*556del
NR_037840.3:n.1908del