Canonical Allele Identifier: CA1308216417

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366305G= , CM000664.2:g.173366305G=	GRCh38
NC_000002.11:g.174231033G= , CM000664.1:g.174231033G=	GRCh37
NC_000002.10:g.173939279G=	NCBI36
NG_047202.1:g.17289G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+713G=	ENSP00000512251.1:n.798+713G=
ENST00000695911.1:c.836G=	ENSP00000512262.1:n.836G=
ENST00000695912.1:c.1055G=	ENSP00000512263.1:p.Arg352=
ENST00000695913.1:c.*1811G=	ENSP00000512264.1:n.*1811G=
ENST00000695914.1:c.818G=	ENSP00000512265.1:p.Arg273=
ENST00000695918.1:n.286G=
ENST00000306721.8:c.1058G= MANE Select	ENSP00000306968.3:p.Arg353=
ENST00000306721.7:c.1058G=	ENSP00000306968.3:p.Arg353=
ENST00000347703.7:c.821G=	ENSP00000272789.4:p.Arg274=
ENST00000410019.3:c.695G=	ENSP00000386833.3:p.Arg232=
ENST00000410101.7:c.926G=	ENSP00000386656.3:p.Arg309=
ENST00000467411.5:n.1768+713G=
ENST00000496441.5:n.1812G=
NM_031942.4:c.1058G=	NP_114148.3:p.Arg353=
NM_145810.2:c.821G=	NP_665809.1:p.Arg274=
XM_011511957.1:c.977G=	XP_011510259.1:p.Arg326=
XR_923034.1:n.1956G=
NM_031942.5:c.1058G= MANE Select	NP_114148.3:p.Arg353=
NM_145810.3:c.821G=	NP_665809.1:p.Arg274=