Canonical Allele Identifier: CA2371931

Gene: CDC25A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48165877G>A , CM000665.2:g.48165877G>A	GRCh38
NC_000003.11:g.48207367G>A , CM000665.1:g.48207367G>A	GRCh37
NC_000003.10:g.48182371G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001789.3:c.1046C>T MANE Select	NP_001780.2:p.Thr349Ile
ENST00000302506.8:c.1046C>T MANE Select	ENSP00000303706.3:p.Thr349Ile
NM_001789.2:c.1046C>T	NP_001780.2:p.Thr349Ile
NM_201567.1:c.926C>T	NP_963861.1:p.Thr309Ile
NM_201567.2:c.926C>T	NP_963861.1:p.Thr309Ile
ENST00000302506.7:c.1046C>T	ENSP00000303706.3:p.Thr349Ile
ENST00000351231.7:c.926C>T	ENSP00000343166.3:p.Thr309Ile
ENST00000459900.1:n.586C>T
XM_006713434.2:c.1043C>T	XP_006713497.1:p.Thr348Ile
XM_006713434.3:c.1043C>T	XP_006713497.1:p.Thr348Ile
XM_006713435.2:c.923C>T	XP_006713498.1:p.Thr308Ile
XM_006713435.3:c.923C>T	XP_006713498.1:p.Thr308Ile
XM_011534316.1:c.1046C>T	XP_011532618.1:p.Thr349Ile
XR_001740392.2:n.1043C>T