Canonical Allele Identifier: CA2810526038

Gene: BIRC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223943_78223944del , CM000679.2:g.78223943_78223944del	GRCh38
NC_000017.10:g.76220024_76220025del , CM000679.1:g.76220024_76220025del	GRCh37
NC_000017.9:g.73731619_73731620del	NCBI36
NG_029069.1:g.14748_14749del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*389_*390del MANE Select	ENSP00000324180.4:n.*389_*390del
ENST00000301633.8:c.*389_*390del	ENSP00000301633.3:n.*389_*390del
ENST00000350051.7:c.*389_*390del	ENSP00000324180.4:n.*389_*390del
ENST00000374948.6:c.*286_*287del	ENSP00000364086.1:n.*286_*287del
NM_001012270.1:c.*286_*287del	NP_001012270.1:n.*286_*287del
NM_001012271.1:c.*389_*390del	NP_001012271.1:n.*389_*390del
NM_001168.2:c.*389_*390del	NP_001159.2:n.*389_*390del
XR_243654.3:n.1020_1021del
XR_934452.1:n.1089_1090del
XR_243654.5:n.1020_1021del
XR_934452.3:n.1089_1090del
NM_001168.3:c.*389_*390del MANE Select	NP_001159.2:n.*389_*390del
NM_001012270.2:c.*286_*287del	NP_001012270.1:n.*286_*287del
NM_001012271.2:c.*389_*390del	NP_001012271.1:n.*389_*390del