Canonical Allele Identifier: CA349330892

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231123G>C (hg19) ; chr2:g.173366395G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366395G>C , CM000664.2:g.173366395G>C	GRCh38
NC_000002.11:g.174231123G>C , CM000664.1:g.174231123G>C	GRCh37
NC_000002.10:g.173939369G>C	NCBI36
NG_047202.1:g.17379G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-755G>C	ENSP00000512251.1:n.799-755G>C
ENST00000695911.1:c.926G>C	ENSP00000512262.1:n.926G>C
ENST00000695912.1:c.1145G>C	ENSP00000512263.1:p.Arg382Pro
ENST00000695913.1:c.*1901G>C	ENSP00000512264.1:n.*1901G>C
ENST00000695914.1:c.908G>C	ENSP00000512265.1:p.Arg303Pro
ENST00000695918.1:n.376G>C
ENST00000306721.8:c.1148G>C MANE Select	ENSP00000306968.3:p.Arg383Pro
ENST00000306721.7:c.1148G>C	ENSP00000306968.3:p.Arg383Pro
ENST00000347703.7:c.911G>C	ENSP00000272789.4:p.Arg304Pro
ENST00000410019.3:c.785G>C	ENSP00000386833.3:p.Arg262Pro
ENST00000410101.7:c.1016G>C	ENSP00000386656.3:p.Arg339Pro
ENST00000467411.5:n.1769-755G>C
ENST00000496441.5:n.1902G>C
NM_031942.4:c.1148G>C	NP_114148.3:p.Arg383Pro
NM_145810.2:c.911G>C	NP_665809.1:p.Arg304Pro
XM_011511957.1:c.1067G>C	XP_011510259.1:p.Arg356Pro
XR_923034.1:n.2046G>C
NM_031942.5:c.1148G>C MANE Select	NP_114148.3:p.Arg383Pro
NM_145810.3:c.911G>C	NP_665809.1:p.Arg304Pro