Canonical Allele Identifier: CA1308216415

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366300A= , CM000664.2:g.173366300A=	GRCh38
NC_000002.11:g.174231028A= , CM000664.1:g.174231028A=	GRCh37
NC_000002.10:g.173939274A=	NCBI36
NG_047202.1:g.17284A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+708A=	ENSP00000512251.1:n.798+708A=
ENST00000695911.1:c.831A=	ENSP00000512262.1:n.831A=
ENST00000695912.1:c.1050A=	ENSP00000512263.1:p.Gln350=
ENST00000695913.1:c.*1806A=	ENSP00000512264.1:n.*1806A=
ENST00000695914.1:c.813A=	ENSP00000512265.1:p.Gln271=
ENST00000695918.1:n.281A=
ENST00000306721.8:c.1053A= MANE Select	ENSP00000306968.3:p.Gln351=
ENST00000306721.7:c.1053A=	ENSP00000306968.3:p.Gln351=
ENST00000347703.7:c.816A=	ENSP00000272789.4:p.Gln272=
ENST00000410019.3:c.690A=	ENSP00000386833.3:p.Gln230=
ENST00000410101.7:c.921A=	ENSP00000386656.3:p.Gln307=
ENST00000467411.5:n.1768+708A=
ENST00000496441.5:n.1807A=
NM_031942.4:c.1053A=	NP_114148.3:p.Gln351=
NM_145810.2:c.816A=	NP_665809.1:p.Gln272=
XM_011511957.1:c.972A=	XP_011510259.1:p.Gln324=
XR_923034.1:n.1951A=
NM_031942.5:c.1053A= MANE Select	NP_114148.3:p.Gln351=
NM_145810.3:c.816A=	NP_665809.1:p.Gln272=