Canonical Allele Identifier: CA1308216422

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366329C= , CM000664.2:g.173366329C=	GRCh38
NC_000002.11:g.174231057C= , CM000664.1:g.174231057C=	GRCh37
NC_000002.10:g.173939303C=	NCBI36
NG_047202.1:g.17313C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+737C=	ENSP00000512251.1:n.798+737C=
ENST00000695911.1:c.860C=	ENSP00000512262.1:n.860C=
ENST00000695912.1:c.1079C=	ENSP00000512263.1:p.Thr360=
ENST00000695913.1:c.*1835C=	ENSP00000512264.1:n.*1835C=
ENST00000695914.1:c.842C=	ENSP00000512265.1:p.Thr281=
ENST00000695918.1:n.310C=
ENST00000306721.8:c.1082C= MANE Select	ENSP00000306968.3:p.Thr361=
ENST00000306721.7:c.1082C=	ENSP00000306968.3:p.Thr361=
ENST00000347703.7:c.845C=	ENSP00000272789.4:p.Thr282=
ENST00000410019.3:c.719C=	ENSP00000386833.3:p.Thr240=
ENST00000410101.7:c.950C=	ENSP00000386656.3:p.Thr317=
ENST00000467411.5:n.1768+737C=
ENST00000496441.5:n.1836C=
NM_031942.4:c.1082C=	NP_114148.3:p.Thr361=
NM_145810.2:c.845C=	NP_665809.1:p.Thr282=
XM_011511957.1:c.1001C=	XP_011510259.1:p.Thr334=
XR_923034.1:n.1980C=
NM_031942.5:c.1082C= MANE Select	NP_114148.3:p.Thr361=
NM_145810.3:c.845C=	NP_665809.1:p.Thr282=