Canonical Allele Identifier: CA1308216452

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366427G= , CM000664.2:g.173366427G=	GRCh38
NC_000002.11:g.174231155G= , CM000664.1:g.174231155G=	GRCh37
NC_000002.10:g.173939401G=	NCBI36
NG_047202.1:g.17411G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-723G=	ENSP00000512251.1:n.799-723G=
ENST00000695911.1:c.958G=	ENSP00000512262.1:n.958G=
ENST00000695912.1:c.1177G=	ENSP00000512263.1:p.Asp393=
ENST00000695913.1:c.*1933G=	ENSP00000512264.1:n.*1933G=
ENST00000695914.1:c.940G=	ENSP00000512265.1:p.Asp314=
ENST00000695918.1:n.408G=
ENST00000306721.8:c.1180G= MANE Select	ENSP00000306968.3:p.Asp394=
ENST00000306721.7:c.1180G=	ENSP00000306968.3:p.Asp394=
ENST00000347703.7:c.943G=	ENSP00000272789.4:p.Asp315=
ENST00000410019.3:c.817G=	ENSP00000386833.3:p.Asp273=
ENST00000410101.7:c.1048G=	ENSP00000386656.3:p.Asp350=
ENST00000467411.5:n.1769-723G=
ENST00000496441.5:n.1934G=
NM_031942.4:c.1180G=	NP_114148.3:p.Asp394=
NM_145810.2:c.943G=	NP_665809.1:p.Asp315=
XM_011511957.1:c.1099G=	XP_011510259.1:p.Asp367=
XR_923034.1:n.2078G=
NM_031942.5:c.1180G= MANE Select	NP_114148.3:p.Asp394=
NM_145810.3:c.943G=	NP_665809.1:p.Asp315=