Canonical Allele Identifier: CA1308216438

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366377G= , CM000664.2:g.173366377G=	GRCh38
NC_000002.11:g.174231105G= , CM000664.1:g.174231105G=	GRCh37
NC_000002.10:g.173939351G=	NCBI36
NG_047202.1:g.17361G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.799-773G=	ENSP00000512251.1:n.799-773G=
ENST00000695911.1:c.908G=	ENSP00000512262.1:n.908G=
ENST00000695912.1:c.1127G=	ENSP00000512263.1:p.Gly376=
ENST00000695913.1:c.*1883G=	ENSP00000512264.1:n.*1883G=
ENST00000695914.1:c.890G=	ENSP00000512265.1:p.Gly297=
ENST00000695918.1:n.358G=
ENST00000306721.8:c.1130G= MANE Select	ENSP00000306968.3:p.Gly377=
ENST00000306721.7:c.1130G=	ENSP00000306968.3:p.Gly377=
ENST00000347703.7:c.893G=	ENSP00000272789.4:p.Gly298=
ENST00000410019.3:c.767G=	ENSP00000386833.3:p.Gly256=
ENST00000410101.7:c.998G=	ENSP00000386656.3:p.Gly333=
ENST00000467411.5:n.1769-773G=
ENST00000496441.5:n.1884G=
NM_031942.4:c.1130G=	NP_114148.3:p.Gly377=
NM_145810.2:c.893G=	NP_665809.1:p.Gly298=
XM_011511957.1:c.1049G=	XP_011510259.1:p.Gly350=
XR_923034.1:n.2028G=
NM_031942.5:c.1130G= MANE Select	NP_114148.3:p.Gly377=
NM_145810.3:c.893G=	NP_665809.1:p.Gly298=