Canonical Allele Identifier: CA2640134769

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78224054-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224055_78224056insTT , CM000679.2:g.78224055_78224056insTT	GRCh38
NC_000017.10:g.76220136_76220137insTT , CM000679.1:g.76220136_76220137insTT	GRCh37
NC_000017.9:g.73731731_73731732insTT	NCBI36
NG_029069.1:g.14860_14861insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*501_*502insTT MANE Select	ENSP00000324180.4:n.*501_*502insTT
ENST00000301633.8:c.*501_*502insTT	ENSP00000301633.3:n.*501_*502insTT
ENST00000350051.7:c.*501_*502insTT	ENSP00000324180.4:n.*501_*502insTT
ENST00000374948.6:c.*398_*399insTT	ENSP00000364086.1:n.*398_*399insTT
NM_001012270.1:c.*398_*399insTT	NP_001012270.1:n.*398_*399insTT
NM_001012271.1:c.*501_*502insTT	NP_001012271.1:n.*501_*502insTT
NM_001168.2:c.*501_*502insTT	NP_001159.2:n.*501_*502insTT
XR_243654.3:n.1132_1133insTT
XR_934452.1:n.1201_1202insTT
XR_243654.5:n.1132_1133insTT
XR_934452.3:n.1201_1202insTT
NM_001168.3:c.*501_*502insTT MANE Select	NP_001159.2:n.*501_*502insTT
NM_001012270.2:c.*398_*399insTT	NP_001012270.1:n.*398_*399insTT
NM_001012271.2:c.*501_*502insTT	NP_001012271.1:n.*501_*502insTT