Canonical Allele Identifier: CA429810481

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231067A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366339A>G , CM000664.2:g.173366339A>G	GRCh38
NC_000002.11:g.174231067A>G , CM000664.1:g.174231067A>G	GRCh37
NC_000002.10:g.173939313A>G	NCBI36
NG_047202.1:g.17323A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+747A>G	ENSP00000512251.1:n.798+747A>G
ENST00000695911.1:c.870A>G	ENSP00000512262.1:n.870A>G
ENST00000695912.1:c.1089A>G	ENSP00000512263.1:p.Arg363=
ENST00000695913.1:c.*1845A>G	ENSP00000512264.1:n.*1845A>G
ENST00000695914.1:c.852A>G	ENSP00000512265.1:p.Arg284=
ENST00000695918.1:n.320A>G
ENST00000306721.8:c.1092A>G MANE Select	ENSP00000306968.3:p.Arg364=
ENST00000306721.7:c.1092A>G	ENSP00000306968.3:p.Arg364=
ENST00000347703.7:c.855A>G	ENSP00000272789.4:p.Arg285=
ENST00000410019.3:c.729A>G	ENSP00000386833.3:p.Arg243=
ENST00000410101.7:c.960A>G	ENSP00000386656.3:p.Arg320=
ENST00000467411.5:n.1768+747A>G
ENST00000496441.5:n.1846A>G
NM_031942.4:c.1092A>G	NP_114148.3:p.Arg364=
NM_145810.2:c.855A>G	NP_665809.1:p.Arg285=
XM_011511957.1:c.1011A>G	XP_011510259.1:p.Arg337=
XR_923034.1:n.1990A>G
NM_031942.5:c.1092A>G MANE Select	NP_114148.3:p.Arg364=
NM_145810.3:c.855A>G	NP_665809.1:p.Arg285=