Canonical Allele Identifier: CA1308216440

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366384C= , CM000664.2:g.173366384C=	GRCh38
NC_000002.11:g.174231112C= , CM000664.1:g.174231112C=	GRCh37
NC_000002.10:g.173939358C=	NCBI36
NG_047202.1:g.17368C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-766C=	ENSP00000512251.1:n.799-766C=
ENST00000695911.1:c.915C=	ENSP00000512262.1:n.915C=
ENST00000695912.1:c.1134C=	ENSP00000512263.1:p.Cys378=
ENST00000695913.1:c.*1890C=	ENSP00000512264.1:n.*1890C=
ENST00000695914.1:c.897C=	ENSP00000512265.1:p.Cys299=
ENST00000695918.1:n.365C=
ENST00000306721.8:c.1137C= MANE Select	ENSP00000306968.3:p.Cys379=
ENST00000306721.7:c.1137C=	ENSP00000306968.3:p.Cys379=
ENST00000347703.7:c.900C=	ENSP00000272789.4:p.Cys300=
ENST00000410019.3:c.774C=	ENSP00000386833.3:p.Cys258=
ENST00000410101.7:c.1005C=	ENSP00000386656.3:p.Cys335=
ENST00000467411.5:n.1769-766C=
ENST00000496441.5:n.1891C=
NM_031942.4:c.1137C=	NP_114148.3:p.Cys379=
NM_145810.2:c.900C=	NP_665809.1:p.Cys300=
XM_011511957.1:c.1056C=	XP_011510259.1:p.Cys352=
XR_923034.1:n.2035C=
NM_031942.5:c.1137C= MANE Select	NP_114148.3:p.Cys379=
NM_145810.3:c.900C=	NP_665809.1:p.Cys300=