Canonical Allele Identifier: CA946933

Gene: CDC7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91515810C>G , CM000663.2:g.91515810C>G	GRCh38
NC_000001.10:g.91981367C>G , CM000663.1:g.91981367C>G	GRCh37
NC_000001.9:g.91753955C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234626.11:c.1114C>G MANE Select	ENSP00000234626.6:p.Pro372Ala
ENST00000234626.10:c.1114C>G	ENSP00000234626.6:p.Pro372Ala
ENST00000428239.5:c.1114C>G	ENSP00000393139.1:p.Pro372Ala
ENST00000486509.1:n.377C>G
NM_001134419.1:c.1114C>G	NP_001127891.1:p.Pro372Ala
NM_001134420.1:c.1114C>G	NP_001127892.1:p.Pro372Ala
NM_003503.3:c.1114C>G	NP_003494.1:p.Pro372Ala
XM_005271241.2:c.1114C>G	XP_005271298.1:p.Pro372Ala
XM_005271244.2:c.1018C>G	XP_005271301.1:p.Pro340Ala
XM_005271245.3:c.*59C>G	XP_005271302.1:n.*59C>G
XM_011542226.1:c.1114C>G	XP_011540528.1:p.Pro372Ala
XM_011542227.1:c.763C>G	XP_011540529.1:p.Pro255Ala
XM_005271244.3:c.1018C>G	XP_005271301.1:p.Pro340Ala
XM_017002425.2:c.1018C>G	XP_016857914.1:p.Pro340Ala
XM_017002426.1:c.1018C>G	XP_016857915.1:p.Pro340Ala
XM_017002427.2:c.763C>G	XP_016857916.1:p.Pro255Ala
XM_024450089.1:c.1114C>G	XP_024305857.1:p.Pro372Ala
XM_024450090.1:c.1114C>G	XP_024305858.1:p.Pro372Ala
XR_001737461.1:n.1331C>G
XR_001737462.1:n.1293C>G
NM_003503.4:c.1114C>G MANE Select	NP_003494.1:p.Pro372Ala
NM_001134419.2:c.1114C>G	NP_001127891.1:p.Pro372Ala
NM_001134420.2:c.1114C>G	NP_001127892.1:p.Pro372Ala