Canonical Allele Identifier: CA986568507

Gene: BIRC5

Linked Data

• gnomAD v3: 17-78224089-G-GTTTTTTT
• gnomAD v4: 17-78224089-G-GTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224089_78224090insTTTTTTT , CM000679.2:g.78224089_78224090insTTTTTTT	GRCh38
NC_000017.10:g.76220170_76220171insTTTTTTT , CM000679.1:g.76220170_76220171insTTTTTTT	GRCh37
NC_000017.9:g.73731765_73731766insTTTTTTT	NCBI36
NG_029069.1:g.14894_14895insTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*535_*536insTTTTTTT MANE Select	ENSP00000324180.4:n.*535_*536insTTTTTTT
ENST00000301633.8:c.*535_*536insTTTTTTT	ENSP00000301633.3:n.*535_*536insTTTTTTT
ENST00000350051.7:c.*535_*536insTTTTTTT	ENSP00000324180.4:n.*535_*536insTTTTTTT
ENST00000374948.6:c.*432_*433insTTTTTTT	ENSP00000364086.1:n.*432_*433insTTTTTTT
NM_001012270.1:c.*432_*433insTTTTTTT	NP_001012270.1:n.*432_*433insTTTTTTT
NM_001012271.1:c.*535_*536insTTTTTTT	NP_001012271.1:n.*535_*536insTTTTTTT
NM_001168.2:c.*535_*536insTTTTTTT	NP_001159.2:n.*535_*536insTTTTTTT
XR_243654.3:n.1166_1167insTTTTTTT
XR_934452.1:n.1235_1236insTTTTTTT
XR_243654.5:n.1166_1167insTTTTTTT
XR_934452.3:n.1235_1236insTTTTTTT
NM_001168.3:c.*535_*536insTTTTTTT MANE Select	NP_001159.2:n.*535_*536insTTTTTTT
NM_001012270.2:c.*432_*433insTTTTTTT	NP_001012270.1:n.*432_*433insTTTTTTT
NM_001012271.2:c.*535_*536insTTTTTTT	NP_001012271.1:n.*535_*536insTTTTTTT