Canonical Allele Identifier: CA2640139168

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78223637-G-GGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223638_78223639insAAG , CM000679.2:g.78223638_78223639insAAG	GRCh38
NC_000017.10:g.76219719_76219720insAAG , CM000679.1:g.76219719_76219720insAAG	GRCh37
NC_000017.9:g.73731314_73731315insAAG	NCBI36
NG_029069.1:g.14443_14444insAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*84_*85insAAG MANE Select	ENSP00000324180.4:n.*84_*85insAAG
ENST00000301633.8:c.*84_*85insAAG	ENSP00000301633.3:n.*84_*85insAAG
ENST00000350051.7:c.*84_*85insAAG	ENSP00000324180.4:n.*84_*85insAAG
ENST00000374948.6:c.395_396insAAG	ENSP00000364086.1:p.Gly132_Pro133insSer
ENST00000589892.1:n.529_530insAAG
NM_001012270.1:c.395_396insAAG	NP_001012270.1:p.Gly132_Pro133insSer
NM_001012271.1:c.*84_*85insAAG	NP_001012271.1:n.*84_*85insAAG
NM_001168.2:c.*84_*85insAAG	NP_001159.2:n.*84_*85insAAG
XR_243654.3:n.715_716insAAG
XR_934452.1:n.784_785insAAG
XR_243654.5:n.715_716insAAG
XR_934452.3:n.784_785insAAG
NM_001168.3:c.*84_*85insAAG MANE Select	NP_001159.2:n.*84_*85insAAG
NM_001012270.2:c.395_396insAAG	NP_001012270.1:p.Gly132_Pro133insSer
NM_001012271.2:c.*84_*85insAAG	NP_001012271.1:n.*84_*85insAAG