Canonical Allele Identifier: CA2672190234
Gene: IL15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733267T>A , CM000666.2:g.141733267T>A GRCh38
NC_000004.11:g.142654420T>A , CM000666.1:g.142654420T>A GRCh37
NC_000004.10:g.142873870T>A NCBI36
NG_029605.1:g.101672T>A
NG_029605.2:g.101672T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*419T>A MANE Select ENSP00000323505.4:n.*419T>A
ENST00000296545.11:c.*419T>A ENSP00000296545.7:n.*419T>A
ENST00000320650.8:c.*419T>A ENSP00000323505.4:n.*419T>A
ENST00000394159.2:c.827T>A ENSP00000377714.1:n.827T>A
ENST00000477265.5:c.*419T>A ENSP00000436914.1:n.*419T>A
NM_000585.4:c.*419T>A NP_000576.1:n.*419T>A
NM_172175.2:c.*419T>A NP_751915.1:n.*419T>A
NR_037840.2:n.1758T>A
NM_000585.5:c.*419T>A MANE Select NP_000576.1:n.*419T>A
NM_172175.3:c.*419T>A NP_751915.1:n.*419T>A
NR_037840.3:n.1771T>A