Canonical Allele Identifier: CA341064689

Gene: CDC7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91514028G>C , CM000663.2:g.91514028G>C	GRCh38
NC_000001.10:g.91979585G>C , CM000663.1:g.91979585G>C	GRCh37
NC_000001.9:g.91752173G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234626.11:c.903G>C MANE Select	ENSP00000234626.6:p.Glu301Asp
ENST00000234626.10:c.903G>C	ENSP00000234626.6:p.Glu301Asp
ENST00000428239.5:c.903G>C	ENSP00000393139.1:p.Glu301Asp
ENST00000486509.1:n.181+721G>C
NM_001134419.1:c.903G>C	NP_001127891.1:p.Glu301Asp
NM_001134420.1:c.903G>C	NP_001127892.1:p.Glu301Asp
NM_003503.3:c.903G>C	NP_003494.1:p.Glu301Asp
XM_005271241.2:c.903G>C	XP_005271298.1:p.Glu301Asp
XM_005271244.2:c.822+721G>C	XP_005271301.1:n.822+721G>C
XM_005271245.3:c.903G>C	XP_005271302.1:p.Glu301Asp
XM_011542226.1:c.903G>C	XP_011540528.1:p.Glu301Asp
XM_011542227.1:c.552G>C	XP_011540529.1:p.Glu184Asp
XM_005271244.3:c.822+721G>C	XP_005271301.1:n.822+721G>C
XM_017002425.2:c.822+721G>C	XP_016857914.1:n.822+721G>C
XM_017002426.1:c.822+721G>C	XP_016857915.1:n.822+721G>C
XM_017002427.2:c.552G>C	XP_016857916.1:p.Glu184Asp
XM_024450089.1:c.903G>C	XP_024305857.1:p.Glu301Asp
XM_024450090.1:c.903G>C	XP_024305858.1:p.Glu301Asp
XR_001737461.1:n.1068G>C
XR_001737462.1:n.1030G>C
NM_003503.4:c.903G>C MANE Select	NP_003494.1:p.Glu301Asp
NM_001134419.2:c.903G>C	NP_001127891.1:p.Glu301Asp
NM_001134420.2:c.903G>C	NP_001127892.1:p.Glu301Asp