Canonical Allele Identifier: CA502084900

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78223766-G-C
• MyVariant Identifiers: chr17:g.76219847G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223766G>C , CM000679.2:g.78223766G>C	GRCh38
NC_000017.10:g.76219847G>C , CM000679.1:g.76219847G>C	GRCh37
NC_000017.9:g.73731442G>C	NCBI36
NG_029069.1:g.14571G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*212G>C MANE Select	ENSP00000324180.4:n.*212G>C
ENST00000301633.8:c.*212G>C	ENSP00000301633.3:n.*212G>C
ENST00000350051.7:c.*212G>C	ENSP00000324180.4:n.*212G>C
ENST00000374948.6:c.*109G>C	ENSP00000364086.1:n.*109G>C
ENST00000589892.1:n.657G>C
NM_001012270.1:c.*109G>C	NP_001012270.1:n.*109G>C
NM_001012271.1:c.*212G>C	NP_001012271.1:n.*212G>C
NM_001168.2:c.*212G>C	NP_001159.2:n.*212G>C
XR_243654.3:n.843G>C
XR_934452.1:n.912G>C
XR_243654.5:n.843G>C
XR_934452.3:n.912G>C
NM_001168.3:c.*212G>C MANE Select	NP_001159.2:n.*212G>C
NM_001012270.2:c.*109G>C	NP_001012270.1:n.*109G>C
NM_001012271.2:c.*212G>C	NP_001012271.1:n.*212G>C