Canonical Allele Identifier: CA429810472

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231052C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366324C>A , CM000664.2:g.173366324C>A	GRCh38
NC_000002.11:g.174231052C>A , CM000664.1:g.174231052C>A	GRCh37
NC_000002.10:g.173939298C>A	NCBI36
NG_047202.1:g.17308C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+732C>A	ENSP00000512251.1:n.798+732C>A
ENST00000695911.1:c.855C>A	ENSP00000512262.1:n.855C>A
ENST00000695912.1:c.1074C>A	ENSP00000512263.1:p.Thr358=
ENST00000695913.1:c.*1830C>A	ENSP00000512264.1:n.*1830C>A
ENST00000695914.1:c.837C>A	ENSP00000512265.1:p.Thr279=
ENST00000695918.1:n.305C>A
ENST00000306721.8:c.1077C>A MANE Select	ENSP00000306968.3:p.Thr359=
ENST00000306721.7:c.1077C>A	ENSP00000306968.3:p.Thr359=
ENST00000347703.7:c.840C>A	ENSP00000272789.4:p.Thr280=
ENST00000410019.3:c.714C>A	ENSP00000386833.3:p.Thr238=
ENST00000410101.7:c.945C>A	ENSP00000386656.3:p.Thr315=
ENST00000467411.5:n.1768+732C>A
ENST00000496441.5:n.1831C>A
NM_031942.4:c.1077C>A	NP_114148.3:p.Thr359=
NM_145810.2:c.840C>A	NP_665809.1:p.Thr280=
XM_011511957.1:c.996C>A	XP_011510259.1:p.Thr332=
XR_923034.1:n.1975C>A
NM_031942.5:c.1077C>A MANE Select	NP_114148.3:p.Thr359=
NM_145810.3:c.840C>A	NP_665809.1:p.Thr280=