Canonical Allele Identifier: CA502084708

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219821C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223740C>G , CM000679.2:g.78223740C>G	GRCh38
NC_000017.10:g.76219821C>G , CM000679.1:g.76219821C>G	GRCh37
NC_000017.9:g.73731416C>G	NCBI36
NG_029069.1:g.14545C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*186C>G MANE Select	ENSP00000324180.4:n.*186C>G
ENST00000301633.8:c.*186C>G	ENSP00000301633.3:n.*186C>G
ENST00000350051.7:c.*186C>G	ENSP00000324180.4:n.*186C>G
ENST00000374948.6:c.*83C>G	ENSP00000364086.1:n.*83C>G
ENST00000589892.1:n.631C>G
NM_001012270.1:c.*83C>G	NP_001012270.1:n.*83C>G
NM_001012271.1:c.*186C>G	NP_001012271.1:n.*186C>G
NM_001168.2:c.*186C>G	NP_001159.2:n.*186C>G
XR_243654.3:n.817C>G
XR_934452.1:n.886C>G
XR_243654.5:n.817C>G
XR_934452.3:n.886C>G
NM_001168.3:c.*186C>G MANE Select	NP_001159.2:n.*186C>G
NM_001012270.2:c.*83C>G	NP_001012270.1:n.*83C>G
NM_001012271.2:c.*186C>G	NP_001012271.1:n.*186C>G