Canonical Allele Identifier: CA8798643
Gene: BIRC5 HGNC NCBI

Linked Data

dbSNP Id: rs112471026

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223565C>T , CM000679.2:g.78223565C>T GRCh38
NC_000017.10:g.76219646C>T , CM000679.1:g.76219646C>T GRCh37
NC_000017.9:g.73731241C>T NCBI36
NG_029069.1:g.14370C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*11C>T MANE Select ENSP00000324180.4:n.*11C>T
ENST00000301633.8:c.*11C>T ENSP00000301633.3:n.*11C>T
ENST00000350051.7:c.*11C>T ENSP00000324180.4:n.*11C>T
ENST00000374948.6:c.322C>T ENSP00000364086.1:p.Arg108Trp
ENST00000589892.1:n.456C>T
NM_001012270.1:c.322C>T NP_001012270.1:p.Arg108Trp
NM_001012271.1:c.*11C>T NP_001012271.1:n.*11C>T
NM_001168.2:c.*11C>T NP_001159.2:n.*11C>T
XR_243654.3:n.642C>T
XR_934452.1:n.711C>T
XR_243654.5:n.642C>T
XR_934452.3:n.711C>T
NM_001168.3:c.*11C>T MANE Select NP_001159.2:n.*11C>T
NM_001012270.2:c.322C>T NP_001012270.1:p.Arg108Trp
NM_001012271.2:c.*11C>T NP_001012271.1:n.*11C>T