Canonical Allele Identifier: CA26659118

Gene: CDC7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91520181G>A , CM000663.2:g.91520181G>A	GRCh38
NC_000001.10:g.91985738G>A , CM000663.1:g.91985738G>A	GRCh37
NC_000001.9:g.91758326G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234626.11:c.1232G>A MANE Select	ENSP00000234626.6:p.Arg411Gln
ENST00000234626.10:c.1232G>A	ENSP00000234626.6:p.Arg411Gln
ENST00000428239.5:c.1232G>A	ENSP00000393139.1:p.Arg411Gln
ENST00000486509.1:n.495G>A
NM_001134419.1:c.1232G>A	NP_001127891.1:p.Arg411Gln
NM_001134420.1:c.1232G>A	NP_001127892.1:p.Arg411Gln
NM_003503.3:c.1232G>A	NP_003494.1:p.Arg411Gln
XM_005271241.2:c.1232G>A	XP_005271298.1:p.Arg411Gln
XM_005271244.2:c.1136G>A	XP_005271301.1:p.Arg379Gln
XM_011542226.1:c.1232G>A	XP_011540528.1:p.Arg411Gln
XM_011542227.1:c.881G>A	XP_011540529.1:p.Arg294Gln
XR_426724.2:n.1091-1506C>T
XM_005271244.3:c.1136G>A	XP_005271301.1:p.Arg379Gln
XM_017002425.2:c.1136G>A	XP_016857914.1:p.Arg379Gln
XM_017002426.1:c.1136G>A	XP_016857915.1:p.Arg379Gln
XM_017002427.2:c.881G>A	XP_016857916.1:p.Arg294Gln
XM_024450089.1:c.1232G>A	XP_024305857.1:p.Arg411Gln
XM_024450090.1:c.1232G>A	XP_024305858.1:p.Arg411Gln
XR_001737461.1:n.1449G>A
XR_001737462.1:n.1411G>A
XR_001738150.2:n.2114-1506C>T
NM_003503.4:c.1232G>A MANE Select	NP_003494.1:p.Arg411Gln
NM_001134419.2:c.1232G>A	NP_001127891.1:p.Arg411Gln
NM_001134420.2:c.1232G>A	NP_001127892.1:p.Arg411Gln