Canonical Allele Identifier: CA1499394757
Gene: IL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733399T= , CM000666.2:g.141733399T= GRCh38
NC_000004.11:g.142654552T= , CM000666.1:g.142654552T= GRCh37
NC_000004.10:g.142874002T= NCBI36
NG_029605.1:g.101804T=
NG_029605.2:g.101804T=

Transcript Alleles

HGVS Amino-acid change
ENST00000320650.9:c.*551T= MANE Select ENSP00000323505.4:n.*551T=
ENST00000296545.11:c.*551T= ENSP00000296545.7:n.*551T=
ENST00000320650.8:c.*551T= ENSP00000323505.4:n.*551T=
ENST00000394159.2:c.959T= ENSP00000377714.1:n.959T=
ENST00000477265.5:c.*551T= ENSP00000436914.1:n.*551T=
NM_000585.4:c.*551T= NP_000576.1:n.*551T=
NM_172175.2:c.*551T= NP_751915.1:n.*551T=
NR_037840.2:n.1890T=
NM_000585.5:c.*551T= MANE Select NP_000576.1:n.*551T=
NM_172175.3:c.*551T= NP_751915.1:n.*551T=
NR_037840.3:n.1903T=