Canonical Allele Identifier: CA74102974

Gene: CDC25A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48182963A>C , CM000665.2:g.48182963A>C	GRCh38
NC_000003.11:g.48224453A>C , CM000665.1:g.48224453A>C	GRCh37
NC_000003.10:g.48199457A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001789.3:c.395T>G MANE Select	NP_001780.2:p.Phe132Cys
ENST00000302506.8:c.395T>G MANE Select	ENSP00000303706.3:p.Phe132Cys
NM_001789.2:c.395T>G	NP_001780.2:p.Phe132Cys
NM_201567.1:c.395T>G	NP_963861.1:p.Phe132Cys
NM_201567.2:c.395T>G	NP_963861.1:p.Phe132Cys
ENST00000302506.7:c.395T>G	ENSP00000303706.3:p.Phe132Cys
ENST00000351231.7:c.395T>G	ENSP00000343166.3:p.Phe132Cys
ENST00000437972.1:c.395T>G	ENSP00000404285.1:p.Phe132Cys
ENST00000443342.5:c.392T>G	ENSP00000416483.1:p.Phe131Cys
XM_006713434.2:c.392T>G	XP_006713497.1:p.Phe131Cys
XM_006713434.3:c.392T>G	XP_006713497.1:p.Phe131Cys
XM_006713435.2:c.392T>G	XP_006713498.1:p.Phe131Cys
XM_006713435.3:c.392T>G	XP_006713498.1:p.Phe131Cys
XM_006713436.2:c.395T>G	XP_006713499.1:p.Phe132Cys
XM_011534316.1:c.395T>G	XP_011532618.1:p.Phe132Cys
XR_001740392.2:n.433T>G