Canonical Allele Identifier: CA1308216436

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366370T= , CM000664.2:g.173366370T=	GRCh38
NC_000002.11:g.174231098T= , CM000664.1:g.174231098T=	GRCh37
NC_000002.10:g.173939344T=	NCBI36
NG_047202.1:g.17354T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+778T=	ENSP00000512251.1:n.798+778T=
ENST00000695911.1:c.901T=	ENSP00000512262.1:n.901T=
ENST00000695912.1:c.1120T=	ENSP00000512263.1:p.Phe374=
ENST00000695913.1:c.*1876T=	ENSP00000512264.1:n.*1876T=
ENST00000695914.1:c.883T=	ENSP00000512265.1:p.Phe295=
ENST00000695918.1:n.351T=
ENST00000306721.8:c.1123T= MANE Select	ENSP00000306968.3:p.Phe375=
ENST00000306721.7:c.1123T=	ENSP00000306968.3:p.Phe375=
ENST00000347703.7:c.886T=	ENSP00000272789.4:p.Phe296=
ENST00000410019.3:c.760T=	ENSP00000386833.3:p.Phe254=
ENST00000410101.7:c.991T=	ENSP00000386656.3:p.Phe331=
ENST00000467411.5:n.1768+778T=
ENST00000496441.5:n.1877T=
NM_031942.4:c.1123T=	NP_114148.3:p.Phe375=
NM_145810.2:c.886T=	NP_665809.1:p.Phe296=
XM_011511957.1:c.1042T=	XP_011510259.1:p.Phe348=
XR_923034.1:n.2021T=
NM_031942.5:c.1123T= MANE Select	NP_114148.3:p.Phe375=
NM_145810.3:c.886T=	NP_665809.1:p.Phe296=