Canonical Allele Identifier: CA9749431

Gene: CDC25B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3802003A>G , CM000682.2:g.3802003A>G	GRCh38
NC_000020.10:g.3782650A>G , CM000682.1:g.3782650A>G	GRCh37
NC_000020.9:g.3730650A>G	NCBI36
NG_029040.2:g.20232A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021873.4:c.1001A>G MANE Select	NP_068659.1:p.Lys334Arg
ENST00000245960.10:c.1001A>G MANE Select	ENSP00000245960.5:p.Lys334Arg
NM_001287516.1:c.809A>G	NP_001274445.1:p.Lys270Arg
NM_001287516.2:c.809A>G	NP_001274445.1:p.Lys270Arg
NM_001287517.1:c.767A>G	NP_001274446.1:p.Lys256Arg
NM_001287517.2:c.767A>G	NP_001274446.1:p.Lys256Arg
NM_001287518.1:c.728A>G	NP_001274447.1:p.Lys243Arg
NM_001287518.2:c.728A>G	NP_001274447.1:p.Lys243Arg
NM_001287519.1:c.665A>G	NP_001274448.1:p.Lys222Arg
NM_001287519.2:c.665A>G	NP_001274448.1:p.Lys222Arg
NM_001287520.1:c.665A>G	NP_001274449.1:p.Lys222Arg
NM_001287520.2:c.665A>G	NP_001274449.1:p.Lys222Arg
NM_001287522.1:c.542A>G	NP_001274451.1:p.Lys181Arg
NM_001287522.2:c.542A>G	NP_001274451.1:p.Lys181Arg
NM_001287524.1:c.425A>G	NP_001274453.1:p.Lys142Arg
NM_001287524.2:c.425A>G	NP_001274453.1:p.Lys142Arg
NM_004358.4:c.959A>G	NP_004349.1:p.Lys320Arg
NM_004358.5:c.959A>G	NP_004349.1:p.Lys320Arg
NM_021872.3:c.878A>G	NP_068658.1:p.Lys293Arg
NM_021872.4:c.878A>G	NP_068658.1:p.Lys293Arg
NM_021873.3:c.1001A>G	NP_068659.1:p.Lys334Arg
NR_136335.1:n.942A>G
NR_136335.2:n.892A>G
NR_136336.1:n.1169A>G
NR_136336.2:n.990A>G
ENST00000245960.9:c.1001A>G	ENSP00000245960.5:p.Lys334Arg
ENST00000340833.4:c.878A>G	ENSP00000339170.4:p.Lys293Arg
ENST00000344256.10:c.809A>G	ENSP00000339125.6:p.Lys270Arg
ENST00000379598.9:c.728A>G	ENSP00000368918.5:p.Lys243Arg
ENST00000439880.6:c.959A>G	ENSP00000405972.2:p.Lys320Arg
ENST00000467519.5:n.942A>G
ENST00000468979.1:n.231A>G
ENST00000480816.5:n.319A>G
XR_937181.1:n.1265A>G
XR_937181.3:n.1070A>G