Canonical Allele Identifier: CA1308216437

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366372C= , CM000664.2:g.173366372C=	GRCh38
NC_000002.11:g.174231100C= , CM000664.1:g.174231100C=	GRCh37
NC_000002.10:g.173939346C=	NCBI36
NG_047202.1:g.17356C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-778C=	ENSP00000512251.1:n.799-778C=
ENST00000695911.1:c.903C=	ENSP00000512262.1:n.903C=
ENST00000695912.1:c.1122C=	ENSP00000512263.1:p.Phe374=
ENST00000695913.1:c.*1878C=	ENSP00000512264.1:n.*1878C=
ENST00000695914.1:c.885C=	ENSP00000512265.1:p.Phe295=
ENST00000695918.1:n.353C=
ENST00000306721.8:c.1125C= MANE Select	ENSP00000306968.3:p.Phe375=
ENST00000306721.7:c.1125C=	ENSP00000306968.3:p.Phe375=
ENST00000347703.7:c.888C=	ENSP00000272789.4:p.Phe296=
ENST00000410019.3:c.762C=	ENSP00000386833.3:p.Phe254=
ENST00000410101.7:c.993C=	ENSP00000386656.3:p.Phe331=
ENST00000467411.5:n.1769-778C=
ENST00000496441.5:n.1879C=
NM_031942.4:c.1125C=	NP_114148.3:p.Phe375=
NM_145810.2:c.888C=	NP_665809.1:p.Phe296=
XM_011511957.1:c.1044C=	XP_011510259.1:p.Phe348=
XR_923034.1:n.2023C=
NM_031942.5:c.1125C= MANE Select	NP_114148.3:p.Phe375=
NM_145810.3:c.888C=	NP_665809.1:p.Phe296=