Canonical Allele Identifier: CA2640134799

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78224067-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224067T>A , CM000679.2:g.78224067T>A	GRCh38
NC_000017.10:g.76220148T>A , CM000679.1:g.76220148T>A	GRCh37
NC_000017.9:g.73731743T>A	NCBI36
NG_029069.1:g.14872T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*513T>A MANE Select	ENSP00000324180.4:n.*513T>A
ENST00000301633.8:c.*513T>A	ENSP00000301633.3:n.*513T>A
ENST00000350051.7:c.*513T>A	ENSP00000324180.4:n.*513T>A
ENST00000374948.6:c.*410T>A	ENSP00000364086.1:n.*410T>A
NM_001012270.1:c.*410T>A	NP_001012270.1:n.*410T>A
NM_001012271.1:c.*513T>A	NP_001012271.1:n.*513T>A
NM_001168.2:c.*513T>A	NP_001159.2:n.*513T>A
XR_243654.3:n.1144T>A
XR_934452.1:n.1213T>A
XR_243654.5:n.1144T>A
XR_934452.3:n.1213T>A
NM_001168.3:c.*513T>A MANE Select	NP_001159.2:n.*513T>A
NM_001012270.2:c.*410T>A	NP_001012270.1:n.*410T>A
NM_001012271.2:c.*513T>A	NP_001012271.1:n.*513T>A