Canonical Allele Identifier: CA107424293

Gene: IL15

Linked Data

• dbSNP Id: rs865856174
• gnomAD v4: 4-141732990-G-A
• MyVariant Identifiers: chr4:g.142654143G>A (hg19) ; chr4:g.141732990G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732990G>A , CM000666.2:g.141732990G>A	GRCh38
NC_000004.11:g.142654143G>A , CM000666.1:g.142654143G>A	GRCh37
NC_000004.10:g.142873593G>A	NCBI36
NG_029605.1:g.101395G>A
NG_029605.2:g.101395G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*142G>A MANE Select	ENSP00000323505.4:n.*142G>A
ENST00000296545.11:c.*142G>A	ENSP00000296545.7:n.*142G>A
ENST00000320650.8:c.*142G>A	ENSP00000323505.4:n.*142G>A
ENST00000394159.2:c.550G>A	ENSP00000377714.1:n.550G>A
ENST00000477265.5:c.*142G>A	ENSP00000436914.1:n.*142G>A
ENST00000514653.5:c.*142G>A	ENSP00000422271.1:n.*142G>A
ENST00000529613.5:c.*142G>A	ENSP00000435462.1:n.*142G>A
NM_000585.4:c.*142G>A	NP_000576.1:n.*142G>A
NM_172175.2:c.*142G>A	NP_751915.1:n.*142G>A
NR_037840.2:n.1481G>A
NM_000585.5:c.*142G>A MANE Select	NP_000576.1:n.*142G>A
NM_172175.3:c.*142G>A	NP_751915.1:n.*142G>A
NR_037840.3:n.1494G>A