Canonical Allele Identifier: CA986568438

Gene: BIRC5

Linked Data

• dbSNP Id: rs2076534153
• gnomAD v3: 17-78224066-T-TG
• gnomAD v4: 17-78224066-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224066_78224067insG , CM000679.2:g.78224066_78224067insG	GRCh38
NC_000017.10:g.76220147_76220148insG , CM000679.1:g.76220147_76220148insG	GRCh37
NC_000017.9:g.73731742_73731743insG	NCBI36
NG_029069.1:g.14871_14872insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*512_*513insG MANE Select	ENSP00000324180.4:n.*512_*513insG
ENST00000301633.8:c.*512_*513insG	ENSP00000301633.3:n.*512_*513insG
ENST00000350051.7:c.*512_*513insG	ENSP00000324180.4:n.*512_*513insG
ENST00000374948.6:c.*409_*410insG	ENSP00000364086.1:n.*409_*410insG
NM_001012270.1:c.*409_*410insG	NP_001012270.1:n.*409_*410insG
NM_001012271.1:c.*512_*513insG	NP_001012271.1:n.*512_*513insG
NM_001168.2:c.*512_*513insG	NP_001159.2:n.*512_*513insG
XR_243654.3:n.1143_1144insG
XR_934452.1:n.1212_1213insG
XR_243654.5:n.1143_1144insG
XR_934452.3:n.1212_1213insG
NM_001168.3:c.*512_*513insG MANE Select	NP_001159.2:n.*512_*513insG
NM_001012270.2:c.*409_*410insG	NP_001012270.1:n.*409_*410insG
NM_001012271.2:c.*512_*513insG	NP_001012271.1:n.*512_*513insG