Canonical Allele Identifier: CA2276860766
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224077_78224078delinsTG , CM000679.2:g.78224077_78224078delinsTG GRCh38
NC_000017.10:g.76220158_76220159delinsTG , CM000679.1:g.76220158_76220159delinsTG GRCh37
NC_000017.9:g.73731753_73731754delinsTG NCBI36
NG_029069.1:g.14882_14883delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*523_*524delinsTG MANE Select ENSP00000324180.4:n.*523_*524delinsTG
ENST00000301633.8:c.*523_*524delinsTG ENSP00000301633.3:n.*523_*524delinsTG
ENST00000350051.7:c.*523_*524delinsTG ENSP00000324180.4:n.*523_*524delinsTG
ENST00000374948.6:c.*420_*421delinsTG ENSP00000364086.1:n.*420_*421delinsTG
NM_001012270.1:c.*420_*421delinsTG NP_001012270.1:n.*420_*421delinsTG
NM_001012271.1:c.*523_*524delinsTG NP_001012271.1:n.*523_*524delinsTG
NM_001168.2:c.*523_*524delinsTG NP_001159.2:n.*523_*524delinsTG
XR_243654.3:n.1154_1155delinsTG
XR_934452.1:n.1223_1224delinsTG
XR_243654.5:n.1154_1155delinsTG
XR_934452.3:n.1223_1224delinsTG
NM_001168.3:c.*523_*524delinsTG MANE Select NP_001159.2:n.*523_*524delinsTG
NM_001012270.2:c.*420_*421delinsTG NP_001012270.1:n.*420_*421delinsTG
NM_001012271.2:c.*523_*524delinsTG NP_001012271.1:n.*523_*524delinsTG