Canonical Allele Identifier: CA349330946

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231133A>C (hg19) ; chr2:g.173366405A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366405A>C , CM000664.2:g.173366405A>C	GRCh38
NC_000002.11:g.174231133A>C , CM000664.1:g.174231133A>C	GRCh37
NC_000002.10:g.173939379A>C	NCBI36
NG_047202.1:g.17389A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-745A>C	ENSP00000512251.1:n.799-745A>C
ENST00000695911.1:c.936A>C	ENSP00000512262.1:n.936A>C
ENST00000695912.1:c.1155A>C	ENSP00000512263.1:p.Glu385Asp
ENST00000695913.1:c.*1911A>C	ENSP00000512264.1:n.*1911A>C
ENST00000695914.1:c.918A>C	ENSP00000512265.1:p.Glu306Asp
ENST00000695918.1:n.386A>C
ENST00000306721.8:c.1158A>C MANE Select	ENSP00000306968.3:p.Glu386Asp
ENST00000306721.7:c.1158A>C	ENSP00000306968.3:p.Glu386Asp
ENST00000347703.7:c.921A>C	ENSP00000272789.4:p.Glu307Asp
ENST00000410019.3:c.795A>C	ENSP00000386833.3:p.Glu265Asp
ENST00000410101.7:c.1026A>C	ENSP00000386656.3:p.Glu342Asp
ENST00000467411.5:n.1769-745A>C
ENST00000496441.5:n.1912A>C
NM_031942.4:c.1158A>C	NP_114148.3:p.Glu386Asp
NM_145810.2:c.921A>C	NP_665809.1:p.Glu307Asp
XM_011511957.1:c.1077A>C	XP_011510259.1:p.Glu359Asp
XR_923034.1:n.2056A>C
NM_031942.5:c.1158A>C MANE Select	NP_114148.3:p.Glu386Asp
NM_145810.3:c.921A>C	NP_665809.1:p.Glu307Asp