Canonical Allele Identifier: CA2276860482

Gene: BIRC5

Linked Data

• dbSNP Id: rs2076528111

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223430G>C , CM000679.2:g.78223430G>C	GRCh38
NC_000017.10:g.76219511G>C , CM000679.1:g.76219511G>C	GRCh37
NC_000017.9:g.73731106G>C	NCBI36
NG_029069.1:g.14235G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.340-35G>C MANE Select	ENSP00000324180.4:n.340-35G>C
ENST00000301633.8:c.409-35G>C	ENSP00000301633.3:n.409-35G>C
ENST00000350051.7:c.340-35G>C	ENSP00000324180.4:n.340-35G>C
ENST00000374948.6:c.222-35G>C	ENSP00000364086.1:n.222-35G>C
ENST00000589892.1:n.356-35G>C
ENST00000590925.6:c.*142-35G>C	ENSP00000467336.1:n.*142-35G>C
NM_001012270.1:c.222-35G>C	NP_001012270.1:n.222-35G>C
NM_001012271.1:c.409-35G>C	NP_001012271.1:n.409-35G>C
NM_001168.2:c.340-35G>C	NP_001159.2:n.340-35G>C
XR_243654.3:n.542-35G>C
XR_934452.1:n.611-35G>C
XR_243654.5:n.542-35G>C
XR_934452.3:n.611-35G>C
NM_001168.3:c.340-35G>C MANE Select	NP_001159.2:n.340-35G>C
NM_001012270.2:c.222-35G>C	NP_001012270.1:n.222-35G>C
NM_001012271.2:c.409-35G>C	NP_001012271.1:n.409-35G>C