Canonical Allele Identifier: CA2372118

Gene: CDC25A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48180836G>C , CM000665.2:g.48180836G>C	GRCh38
NC_000003.11:g.48222326G>C , CM000665.1:g.48222326G>C	GRCh37
NC_000003.10:g.48197330G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001789.3:c.434C>G MANE Select	NP_001780.2:p.Ala145Gly
ENST00000302506.8:c.434C>G MANE Select	ENSP00000303706.3:p.Ala145Gly
NM_001789.2:c.434C>G	NP_001780.2:p.Ala145Gly
NM_201567.1:c.429+2093C>G	NP_963861.1:n.429+2093C>G
NM_201567.2:c.429+2093C>G	NP_963861.1:n.429+2093C>G
ENST00000302506.7:c.434C>G	ENSP00000303706.3:p.Ala145Gly
ENST00000351231.7:c.429+2093C>G	ENSP00000343166.3:n.429+2093C>G
ENST00000443342.5:c.431C>G	ENSP00000416483.1:p.Ala144Gly
XM_006713434.2:c.431C>G	XP_006713497.1:p.Ala144Gly
XM_006713434.3:c.431C>G	XP_006713497.1:p.Ala144Gly
XM_006713435.2:c.426+2093C>G	XP_006713498.1:n.426+2093C>G
XM_006713435.3:c.426+2093C>G	XP_006713498.1:n.426+2093C>G
XM_006713436.2:c.434C>G	XP_006713499.1:p.Ala145Gly
XM_011534316.1:c.434C>G	XP_011532618.1:p.Ala145Gly
XR_001740392.2:n.472C>G