Canonical Allele Identifier: CA349330933

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231131G>C (hg19) ; chr2:g.173366403G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366403G>C , CM000664.2:g.173366403G>C	GRCh38
NC_000002.11:g.174231131G>C , CM000664.1:g.174231131G>C	GRCh37
NC_000002.10:g.173939377G>C	NCBI36
NG_047202.1:g.17387G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-747G>C	ENSP00000512251.1:n.799-747G>C
ENST00000695911.1:c.934G>C	ENSP00000512262.1:n.934G>C
ENST00000695912.1:c.1153G>C	ENSP00000512263.1:p.Glu385Gln
ENST00000695913.1:c.*1909G>C	ENSP00000512264.1:n.*1909G>C
ENST00000695914.1:c.916G>C	ENSP00000512265.1:p.Glu306Gln
ENST00000695918.1:n.384G>C
ENST00000306721.8:c.1156G>C MANE Select	ENSP00000306968.3:p.Glu386Gln
ENST00000306721.7:c.1156G>C	ENSP00000306968.3:p.Glu386Gln
ENST00000347703.7:c.919G>C	ENSP00000272789.4:p.Glu307Gln
ENST00000410019.3:c.793G>C	ENSP00000386833.3:p.Glu265Gln
ENST00000410101.7:c.1024G>C	ENSP00000386656.3:p.Glu342Gln
ENST00000467411.5:n.1769-747G>C
ENST00000496441.5:n.1910G>C
NM_031942.4:c.1156G>C	NP_114148.3:p.Glu386Gln
NM_145810.2:c.919G>C	NP_665809.1:p.Glu307Gln
XM_011511957.1:c.1075G>C	XP_011510259.1:p.Glu359Gln
XR_923034.1:n.2054G>C
NM_031942.5:c.1156G>C MANE Select	NP_114148.3:p.Glu386Gln
NM_145810.3:c.919G>C	NP_665809.1:p.Glu307Gln