Canonical Allele Identifier: CA6247332
Gene: BIRC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102377646C>T , CM000673.2:g.102377646C>T GRCh38
NC_000011.9:g.102248377C>T , CM000673.1:g.102248377C>T GRCh37
NC_000011.8:g.101753587C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001166.5:c.1517C>T MANE Select NP_001157.1:p.Ala506Val
ENST00000227758.7:c.1517C>T MANE Select ENSP00000227758.2:p.Ala506Val
NM_001166.4:c.1517C>T NP_001157.1:p.Ala506Val
NM_001256163.1:c.1517C>T NP_001243092.1:p.Ala506Val
NM_001256166.1:c.1370C>T NP_001243095.1:p.Ala457Val
NM_001256166.2:c.1370C>T NP_001243095.1:p.Ala457Val
ENST00000227758.6:c.1517C>T ENSP00000227758.2:p.Ala506Val
ENST00000527910.5:n.3246C>T
ENST00000530675.5:c.1370C>T ENSP00000431723.1:p.Ala457Val
ENST00000531259.5:c.122C>T ENSP00000436741.1:p.Ala41Val
ENST00000532672.5:c.1454C>T ENSP00000434979.1:p.Ala485Val
ENST00000533742.5:c.503C>T ENSP00000433851.1:p.Ala168Val
ENST00000613397.4:c.1517C>T ENSP00000477613.1:p.Ala506Val
ENST00000621637.1:c.1517C>T ENSP00000484838.1:p.Ala506Val