Canonical Allele Identifier: CA429810500

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231097G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366369G>A , CM000664.2:g.173366369G>A	GRCh38
NC_000002.11:g.174231097G>A , CM000664.1:g.174231097G>A	GRCh37
NC_000002.10:g.173939343G>A	NCBI36
NG_047202.1:g.17353G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+777G>A	ENSP00000512251.1:n.798+777G>A
ENST00000695911.1:c.900G>A	ENSP00000512262.1:n.900G>A
ENST00000695912.1:c.1119G>A	ENSP00000512263.1:p.Gln373=
ENST00000695913.1:c.*1875G>A	ENSP00000512264.1:n.*1875G>A
ENST00000695914.1:c.882G>A	ENSP00000512265.1:p.Gln294=
ENST00000695918.1:n.350G>A
ENST00000306721.8:c.1122G>A MANE Select	ENSP00000306968.3:p.Gln374=
ENST00000306721.7:c.1122G>A	ENSP00000306968.3:p.Gln374=
ENST00000347703.7:c.885G>A	ENSP00000272789.4:p.Gln295=
ENST00000410019.3:c.759G>A	ENSP00000386833.3:p.Gln253=
ENST00000410101.7:c.990G>A	ENSP00000386656.3:p.Gln330=
ENST00000467411.5:n.1768+777G>A
ENST00000496441.5:n.1876G>A
NM_031942.4:c.1122G>A	NP_114148.3:p.Gln374=
NM_145810.2:c.885G>A	NP_665809.1:p.Gln295=
XM_011511957.1:c.1041G>A	XP_011510259.1:p.Gln347=
XR_923034.1:n.2020G>A
NM_031942.5:c.1122G>A MANE Select	NP_114148.3:p.Gln374=
NM_145810.3:c.885G>A	NP_665809.1:p.Gln295=