Canonical Allele Identifier: CA401215210
Gene: BIRC5 HGNC NCBI

Linked Data

dbSNP Id: rs760508738

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223556G>C , CM000679.2:g.78223556G>C GRCh38
NC_000017.10:g.76219637G>C , CM000679.1:g.76219637G>C GRCh37
NC_000017.9:g.73731232G>C NCBI36
NG_029069.1:g.14361G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*2G>C MANE Select ENSP00000324180.4:n.*2G>C
ENST00000301633.8:c.*2G>C ENSP00000301633.3:n.*2G>C
ENST00000350051.7:c.*2G>C ENSP00000324180.4:n.*2G>C
ENST00000374948.6:c.313G>C ENSP00000364086.1:p.Ala105Pro
ENST00000589892.1:n.447G>C
NM_001012270.1:c.313G>C NP_001012270.1:p.Ala105Pro
NM_001012271.1:c.*2G>C NP_001012271.1:n.*2G>C
NM_001168.2:c.*2G>C NP_001159.2:n.*2G>C
XR_243654.3:n.633G>C
XR_934452.1:n.702G>C
XR_243654.5:n.633G>C
XR_934452.3:n.702G>C
NM_001168.3:c.*2G>C MANE Select NP_001159.2:n.*2G>C
NM_001012270.2:c.313G>C NP_001012270.1:p.Ala105Pro
NM_001012271.2:c.*2G>C NP_001012271.1:n.*2G>C