Canonical Allele Identifier: CA15346988
Gene: IL15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141649319G>A , CM000666.2:g.141649319G>A GRCh38
NC_000004.11:g.142570472G>A , CM000666.1:g.142570472G>A GRCh37
NC_000004.10:g.142789922G>A NCBI36
NG_029605.1:g.17724G>A
NG_029605.2:g.17724G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.-221-6867G>A MANE Select ENSP00000323505.4:n.-221-6867G>A
ENST00000296545.11:c.-221-6867G>A ENSP00000296545.7:n.-221-6867G>A
ENST00000320650.8:c.-221-6867G>A ENSP00000323505.4:n.-221-6867G>A
ENST00000514653.5:c.-623-6867G>A ENSP00000422271.1:n.-623-6867G>A
ENST00000529613.5:c.-314+12095G>A ENSP00000435462.1:n.-314+12095G>A
NM_000585.4:c.-221-6867G>A NP_000576.1:n.-221-6867G>A
NM_172175.2:c.-623-6867G>A NP_751915.1:n.-623-6867G>A
NR_037840.2:n.630-6867G>A
NM_000585.5:c.-221-6867G>A MANE Select NP_000576.1:n.-221-6867G>A
NM_172175.3:c.-623-6867G>A NP_751915.1:n.-623-6867G>A
NR_037840.3:n.643-6867G>A
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