Canonical Allele Identifier: CA294307385

Gene: BIRC5

Linked Data

• dbSNP Id: rs923214582
• gnomAD v3: 17-78223989-A-G
• gnomAD v4: 17-78223989-A-G
• MyVariant Identifiers: chr17:g.76220070A>G (hg19) ; chr17:g.78223989A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223989A>G , CM000679.2:g.78223989A>G	GRCh38
NC_000017.10:g.76220070A>G , CM000679.1:g.76220070A>G	GRCh37
NC_000017.9:g.73731665A>G	NCBI36
NG_029069.1:g.14794A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*435A>G MANE Select	ENSP00000324180.4:n.*435A>G
ENST00000301633.8:c.*435A>G	ENSP00000301633.3:n.*435A>G
ENST00000350051.7:c.*435A>G	ENSP00000324180.4:n.*435A>G
ENST00000374948.6:c.*332A>G	ENSP00000364086.1:n.*332A>G
NM_001012270.1:c.*332A>G	NP_001012270.1:n.*332A>G
NM_001012271.1:c.*435A>G	NP_001012271.1:n.*435A>G
NM_001168.2:c.*435A>G	NP_001159.2:n.*435A>G
XR_243654.3:n.1066A>G
XR_934452.1:n.1135A>G
XR_243654.5:n.1066A>G
XR_934452.3:n.1135A>G
NM_001168.3:c.*435A>G MANE Select	NP_001159.2:n.*435A>G
NM_001012270.2:c.*332A>G	NP_001012270.1:n.*332A>G
NM_001012271.2:c.*435A>G	NP_001012271.1:n.*435A>G