Canonical Allele Identifier: CA2763807983
Gene: IL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733421A>T , CM000666.2:g.141733421A>T GRCh38
NC_000004.11:g.142654574A>T , CM000666.1:g.142654574A>T GRCh37
NC_000004.10:g.142874024A>T NCBI36
NG_029605.1:g.101826A>T
NG_029605.2:g.101826A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*573A>T MANE Select ENSP00000323505.4:n.*573A>T
ENST00000296545.11:c.*573A>T ENSP00000296545.7:n.*573A>T
ENST00000320650.8:c.*573A>T ENSP00000323505.4:n.*573A>T
ENST00000394159.2:c.981A>T ENSP00000377714.1:n.981A>T
ENST00000477265.5:c.*573A>T ENSP00000436914.1:n.*573A>T
NM_000585.4:c.*573A>T NP_000576.1:n.*573A>T
NM_172175.2:c.*573A>T NP_751915.1:n.*573A>T
NR_037840.2:n.1912A>T
NM_000585.5:c.*573A>T MANE Select NP_000576.1:n.*573A>T
NM_172175.3:c.*573A>T NP_751915.1:n.*573A>T
NR_037840.3:n.1925A>T