Canonical Allele Identifier: CA919900877
Gene: BIRC5 HGNC NCBI

Linked Data

dbSNP Id: rs1555610821

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224053_78224056delinsGTT , CM000679.2:g.78224053_78224056delinsGTT GRCh38
NC_000017.10:g.76220134_76220137delinsGTT , CM000679.1:g.76220134_76220137delinsGTT GRCh37
NC_000017.9:g.73731729_73731732delinsGTT NCBI36
NG_029069.1:g.14858_14861delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*499_*502delinsGTT MANE Select ENSP00000324180.4:n.*499_*502delinsGTT
ENST00000301633.8:c.*499_*502delinsGTT ENSP00000301633.3:n.*499_*502delinsGTT
ENST00000350051.7:c.*499_*502delinsGTT ENSP00000324180.4:n.*499_*502delinsGTT
ENST00000374948.6:c.*396_*399delinsGTT ENSP00000364086.1:n.*396_*399delinsGTT
NM_001012270.1:c.*396_*399delinsGTT NP_001012270.1:n.*396_*399delinsGTT
NM_001012271.1:c.*499_*502delinsGTT NP_001012271.1:n.*499_*502delinsGTT
NM_001168.2:c.*499_*502delinsGTT NP_001159.2:n.*499_*502delinsGTT
XR_243654.3:n.1130_1133delinsGTT
XR_934452.1:n.1199_1202delinsGTT
XR_243654.5:n.1130_1133delinsGTT
XR_934452.3:n.1199_1202delinsGTT
NM_001168.3:c.*499_*502delinsGTT MANE Select NP_001159.2:n.*499_*502delinsGTT
NM_001012270.2:c.*396_*399delinsGTT NP_001012270.1:n.*396_*399delinsGTT
NM_001012271.2:c.*499_*502delinsGTT NP_001012271.1:n.*499_*502delinsGTT