Canonical Allele Identifier: CA1499394437
Gene: IL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733011G= , CM000666.2:g.141733011G= GRCh38
NC_000004.11:g.142654164G= , CM000666.1:g.142654164G= GRCh37
NC_000004.10:g.142873614G= NCBI36
NG_029605.1:g.101416G=
NG_029605.2:g.101416G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*163G= MANE Select ENSP00000323505.4:n.*163G=
ENST00000296545.11:c.*163G= ENSP00000296545.7:n.*163G=
ENST00000320650.8:c.*163G= ENSP00000323505.4:n.*163G=
ENST00000394159.2:c.571G= ENSP00000377714.1:n.571G=
ENST00000477265.5:c.*163G= ENSP00000436914.1:n.*163G=
ENST00000514653.5:c.*163G= ENSP00000422271.1:n.*163G=
ENST00000529613.5:c.*163G= ENSP00000435462.1:n.*163G=
NM_000585.4:c.*163G= NP_000576.1:n.*163G=
NM_172175.2:c.*163G= NP_751915.1:n.*163G=
NR_037840.2:n.1502G=
NM_000585.5:c.*163G= MANE Select NP_000576.1:n.*163G=
NM_172175.3:c.*163G= NP_751915.1:n.*163G=
NR_037840.3:n.1515G=