Canonical Allele Identifier: CA2276860695
Gene: BIRC5 HGNC NCBI

Linked Data

dbSNP Id: rs1599034127

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224032A>G , CM000679.2:g.78224032A>G GRCh38
NC_000017.10:g.76220113A>G , CM000679.1:g.76220113A>G GRCh37
NC_000017.9:g.73731708A>G NCBI36
NG_029069.1:g.14837A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*478A>G MANE Select ENSP00000324180.4:n.*478A>G
ENST00000301633.8:c.*478A>G ENSP00000301633.3:n.*478A>G
ENST00000350051.7:c.*478A>G ENSP00000324180.4:n.*478A>G
ENST00000374948.6:c.*375A>G ENSP00000364086.1:n.*375A>G
NM_001012270.1:c.*375A>G NP_001012270.1:n.*375A>G
NM_001012271.1:c.*478A>G NP_001012271.1:n.*478A>G
NM_001168.2:c.*478A>G NP_001159.2:n.*478A>G
XR_243654.3:n.1109A>G
XR_934452.1:n.1178A>G
XR_243654.5:n.1109A>G
XR_934452.3:n.1178A>G
NM_001168.3:c.*478A>G MANE Select NP_001159.2:n.*478A>G
NM_001012270.2:c.*375A>G NP_001012270.1:n.*375A>G
NM_001012271.2:c.*478A>G NP_001012271.1:n.*478A>G