Canonical Allele Identifier: CA2276860603

Gene: BIRC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223765_78223766delinsAG , CM000679.2:g.78223765_78223766delinsAG	GRCh38
NC_000017.10:g.76219846_76219847delinsAG , CM000679.1:g.76219846_76219847delinsAG	GRCh37
NC_000017.9:g.73731441_73731442delinsAG	NCBI36
NG_029069.1:g.14570_14571delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*211_*212delinsAG MANE Select	ENSP00000324180.4:n.*211_*212delinsAG
ENST00000301633.8:c.*211_*212delinsAG	ENSP00000301633.3:n.*211_*212delinsAG
ENST00000350051.7:c.*211_*212delinsAG	ENSP00000324180.4:n.*211_*212delinsAG
ENST00000374948.6:c.*108_*109delinsAG	ENSP00000364086.1:n.*108_*109delinsAG
ENST00000589892.1:n.656_657delinsAG
NM_001012270.1:c.*108_*109delinsAG	NP_001012270.1:n.*108_*109delinsAG
NM_001012271.1:c.*211_*212delinsAG	NP_001012271.1:n.*211_*212delinsAG
NM_001168.2:c.*211_*212delinsAG	NP_001159.2:n.*211_*212delinsAG
XR_243654.3:n.842_843delinsAG
XR_934452.1:n.911_912delinsAG
XR_243654.5:n.842_843delinsAG
XR_934452.3:n.911_912delinsAG
NM_001168.3:c.*211_*212delinsAG MANE Select	NP_001159.2:n.*211_*212delinsAG
NM_001012270.2:c.*108_*109delinsAG	NP_001012270.1:n.*108_*109delinsAG
NM_001012271.2:c.*211_*212delinsAG	NP_001012271.1:n.*211_*212delinsAG