Canonical Allele Identifier: CA986568459

Gene: BIRC5

Linked Data

• gnomAD v3: 17-78224079-G-GTTTTTTTTTTTTTTTTTT
• gnomAD v4: 17-78224079-G-GTTTTTTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224080_78224081insTTTTTTTTTTTTTTTTTT , CM000679.2:g.78224080_78224081insTTTTTTTTTTTTTTTTTT	GRCh38
NC_000017.10:g.76220161_76220162insTTTTTTTTTTTTTTTTTT , CM000679.1:g.76220161_76220162insTTTTTTTTTTTTTTTTTT	GRCh37
NC_000017.9:g.73731756_73731757insTTTTTTTTTTTTTTTTTT	NCBI36
NG_029069.1:g.14885_14886insTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*526_*527insTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000324180.4:n.*526_*527insTTTTTTTTTTTTTTTTTT
ENST00000301633.8:c.*526_*527insTTTTTTTTTTTTTTTTTT	ENSP00000301633.3:n.*526_*527insTTTTTTTTTTTTTTTTTT
ENST00000350051.7:c.*526_*527insTTTTTTTTTTTTTTTTTT	ENSP00000324180.4:n.*526_*527insTTTTTTTTTTTTTTTTTT
ENST00000374948.6:c.*423_*424insTTTTTTTTTTTTTTTTTT	ENSP00000364086.1:n.*423_*424insTTTTTTTTTTTTTTTTTT
NM_001012270.1:c.*423_*424insTTTTTTTTTTTTTTTTTT	NP_001012270.1:n.*423_*424insTTTTTTTTTTTTTTTTTT
NM_001012271.1:c.*526_*527insTTTTTTTTTTTTTTTTTT	NP_001012271.1:n.*526_*527insTTTTTTTTTTTTTTTTTT
NM_001168.2:c.*526_*527insTTTTTTTTTTTTTTTTTT	NP_001159.2:n.*526_*527insTTTTTTTTTTTTTTTTTT
XR_243654.3:n.1157_1158insTTTTTTTTTTTTTTTTTT
XR_934452.1:n.1226_1227insTTTTTTTTTTTTTTTTTT
XR_243654.5:n.1157_1158insTTTTTTTTTTTTTTTTTT
XR_934452.3:n.1226_1227insTTTTTTTTTTTTTTTTTT
NM_001168.3:c.*526_*527insTTTTTTTTTTTTTTTTTT MANE Select	NP_001159.2:n.*526_*527insTTTTTTTTTTTTTTTTTT
NM_001012270.2:c.*423_*424insTTTTTTTTTTTTTTTTTT	NP_001012270.1:n.*423_*424insTTTTTTTTTTTTTTTTTT
NM_001012271.2:c.*526_*527insTTTTTTTTTTTTTTTTTT	NP_001012271.1:n.*526_*527insTTTTTTTTTTTTTTTTTT