Canonical Allele Identifier: CA1308216418

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366316A= , CM000664.2:g.173366316A=	GRCh38
NC_000002.11:g.174231044A= , CM000664.1:g.174231044A=	GRCh37
NC_000002.10:g.173939290A=	NCBI36
NG_047202.1:g.17300A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+724A=	ENSP00000512251.1:n.798+724A=
ENST00000695911.1:c.847A=	ENSP00000512262.1:n.847A=
ENST00000695912.1:c.1066A=	ENSP00000512263.1:p.Ile356=
ENST00000695913.1:c.*1822A=	ENSP00000512264.1:n.*1822A=
ENST00000695914.1:c.829A=	ENSP00000512265.1:p.Ile277=
ENST00000695918.1:n.297A=
ENST00000306721.8:c.1069A= MANE Select	ENSP00000306968.3:p.Ile357=
ENST00000306721.7:c.1069A=	ENSP00000306968.3:p.Ile357=
ENST00000347703.7:c.832A=	ENSP00000272789.4:p.Ile278=
ENST00000410019.3:c.706A=	ENSP00000386833.3:p.Ile236=
ENST00000410101.7:c.937A=	ENSP00000386656.3:p.Ile313=
ENST00000467411.5:n.1768+724A=
ENST00000496441.5:n.1823A=
NM_031942.4:c.1069A=	NP_114148.3:p.Ile357=
NM_145810.2:c.832A=	NP_665809.1:p.Ile278=
XM_011511957.1:c.988A=	XP_011510259.1:p.Ile330=
XR_923034.1:n.1967A=
NM_031942.5:c.1069A= MANE Select	NP_114148.3:p.Ile357=
NM_145810.3:c.832A=	NP_665809.1:p.Ile278=