Canonical Allele Identifier: CA1308216435

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366366C= , CM000664.2:g.173366366C=	GRCh38
NC_000002.11:g.174231094C= , CM000664.1:g.174231094C=	GRCh37
NC_000002.10:g.173939340C=	NCBI36
NG_047202.1:g.17350C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+774C=	ENSP00000512251.1:n.798+774C=
ENST00000695911.1:c.897C=	ENSP00000512262.1:n.897C=
ENST00000695912.1:c.1116C=	ENSP00000512263.1:p.Gly372=
ENST00000695913.1:c.*1872C=	ENSP00000512264.1:n.*1872C=
ENST00000695914.1:c.879C=	ENSP00000512265.1:p.Gly293=
ENST00000695918.1:n.347C=
ENST00000306721.8:c.1119C= MANE Select	ENSP00000306968.3:p.Gly373=
ENST00000306721.7:c.1119C=	ENSP00000306968.3:p.Gly373=
ENST00000347703.7:c.882C=	ENSP00000272789.4:p.Gly294=
ENST00000410019.3:c.756C=	ENSP00000386833.3:p.Gly252=
ENST00000410101.7:c.987C=	ENSP00000386656.3:p.Gly329=
ENST00000467411.5:n.1768+774C=
ENST00000496441.5:n.1873C=
NM_031942.4:c.1119C=	NP_114148.3:p.Gly373=
NM_145810.2:c.882C=	NP_665809.1:p.Gly294=
XM_011511957.1:c.1038C=	XP_011510259.1:p.Gly346=
XR_923034.1:n.2017C=
NM_031942.5:c.1119C= MANE Select	NP_114148.3:p.Gly373=
NM_145810.3:c.882C=	NP_665809.1:p.Gly294=