Canonical Allele Identifier: CA1308216416

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366304C= , CM000664.2:g.173366304C=	GRCh38
NC_000002.11:g.174231032C= , CM000664.1:g.174231032C=	GRCh37
NC_000002.10:g.173939278C=	NCBI36
NG_047202.1:g.17288C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+712C=	ENSP00000512251.1:n.798+712C=
ENST00000695911.1:c.835C=	ENSP00000512262.1:n.835C=
ENST00000695912.1:c.1054C=	ENSP00000512263.1:p.Arg352=
ENST00000695913.1:c.*1810C=	ENSP00000512264.1:n.*1810C=
ENST00000695914.1:c.817C=	ENSP00000512265.1:p.Arg273=
ENST00000695918.1:n.285C=
ENST00000306721.8:c.1057C= MANE Select	ENSP00000306968.3:p.Arg353=
ENST00000306721.7:c.1057C=	ENSP00000306968.3:p.Arg353=
ENST00000347703.7:c.820C=	ENSP00000272789.4:p.Arg274=
ENST00000410019.3:c.694C=	ENSP00000386833.3:p.Arg232=
ENST00000410101.7:c.925C=	ENSP00000386656.3:p.Arg309=
ENST00000467411.5:n.1768+712C=
ENST00000496441.5:n.1811C=
NM_031942.4:c.1057C=	NP_114148.3:p.Arg353=
NM_145810.2:c.820C=	NP_665809.1:p.Arg274=
XM_011511957.1:c.976C=	XP_011510259.1:p.Arg326=
XR_923034.1:n.1955C=
NM_031942.5:c.1057C= MANE Select	NP_114148.3:p.Arg353=
NM_145810.3:c.820C=	NP_665809.1:p.Arg274=