Canonical Allele Identifier: CA429810523

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231133A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-745A>G	ENSP00000512251.1:n.799-745A>G
ENST00000695911.1:c.936A>G	ENSP00000512262.1:n.936A>G
ENST00000695912.1:c.1155A>G	ENSP00000512263.1:p.Glu385=
ENST00000695913.1:c.*1911A>G	ENSP00000512264.1:n.*1911A>G
ENST00000695914.1:c.918A>G	ENSP00000512265.1:p.Glu306=
ENST00000695918.1:n.386A>G
ENST00000306721.8:c.1158A>G MANE Select	ENSP00000306968.3:p.Glu386=
ENST00000306721.7:c.1158A>G	ENSP00000306968.3:p.Glu386=
ENST00000347703.7:c.921A>G	ENSP00000272789.4:p.Glu307=
ENST00000410019.3:c.795A>G	ENSP00000386833.3:p.Glu265=
ENST00000410101.7:c.1026A>G	ENSP00000386656.3:p.Glu342=
ENST00000467411.5:n.1769-745A>G
ENST00000496441.5:n.1912A>G
NM_031942.4:c.1158A>G	NP_114148.3:p.Glu386=
NM_145810.2:c.921A>G	NP_665809.1:p.Glu307=
XM_011511957.1:c.1077A>G	XP_011510259.1:p.Glu359=
XR_923034.1:n.2056A>G
NM_031942.5:c.1158A>G MANE Select	NP_114148.3:p.Glu386=
NM_145810.3:c.921A>G	NP_665809.1:p.Glu307=