Canonical Allele Identifier: CA1499394588
Gene: IL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733203G= , CM000666.2:g.141733203G= GRCh38
NC_000004.11:g.142654356G= , CM000666.1:g.142654356G= GRCh37
NC_000004.10:g.142873806G= NCBI36
NG_029605.1:g.101608G=
NG_029605.2:g.101608G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*355G= MANE Select ENSP00000323505.4:n.*355G=
ENST00000296545.11:c.*355G= ENSP00000296545.7:n.*355G=
ENST00000320650.8:c.*355G= ENSP00000323505.4:n.*355G=
ENST00000394159.2:c.763G= ENSP00000377714.1:n.763G=
ENST00000477265.5:c.*355G= ENSP00000436914.1:n.*355G=
NM_000585.4:c.*355G= NP_000576.1:n.*355G=
NM_172175.2:c.*355G= NP_751915.1:n.*355G=
NR_037840.2:n.1694G=
NM_000585.5:c.*355G= MANE Select NP_000576.1:n.*355G=
NM_172175.3:c.*355G= NP_751915.1:n.*355G=
NR_037840.3:n.1707G=