Canonical Allele Identifier: CA429810502

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231106C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366378C>A , CM000664.2:g.173366378C>A	GRCh38
NC_000002.11:g.174231106C>A , CM000664.1:g.174231106C>A	GRCh37
NC_000002.10:g.173939352C>A	NCBI36
NG_047202.1:g.17362C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.799-772C>A	ENSP00000512251.1:n.799-772C>A
ENST00000695911.1:c.909C>A	ENSP00000512262.1:n.909C>A
ENST00000695912.1:c.1128C>A	ENSP00000512263.1:p.Gly376=
ENST00000695913.1:c.*1884C>A	ENSP00000512264.1:n.*1884C>A
ENST00000695914.1:c.891C>A	ENSP00000512265.1:p.Gly297=
ENST00000695918.1:n.359C>A
ENST00000306721.8:c.1131C>A MANE Select	ENSP00000306968.3:p.Gly377=
ENST00000306721.7:c.1131C>A	ENSP00000306968.3:p.Gly377=
ENST00000347703.7:c.894C>A	ENSP00000272789.4:p.Gly298=
ENST00000410019.3:c.768C>A	ENSP00000386833.3:p.Gly256=
ENST00000410101.7:c.999C>A	ENSP00000386656.3:p.Gly333=
ENST00000467411.5:n.1769-772C>A
ENST00000496441.5:n.1885C>A
NM_031942.4:c.1131C>A	NP_114148.3:p.Gly377=
NM_145810.2:c.894C>A	NP_665809.1:p.Gly298=
XM_011511957.1:c.1050C>A	XP_011510259.1:p.Gly350=
XR_923034.1:n.2029C>A
NM_031942.5:c.1131C>A MANE Select	NP_114148.3:p.Gly377=
NM_145810.3:c.894C>A	NP_665809.1:p.Gly298=