Canonical Allele Identifier: CA349330590

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231065A>G (hg19) ; chr2:g.173366337A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366337A>G , CM000664.2:g.173366337A>G	GRCh38
NC_000002.11:g.174231065A>G , CM000664.1:g.174231065A>G	GRCh37
NC_000002.10:g.173939311A>G	NCBI36
NG_047202.1:g.17321A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+745A>G	ENSP00000512251.1:n.798+745A>G
ENST00000695911.1:c.868A>G	ENSP00000512262.1:n.868A>G
ENST00000695912.1:c.1087A>G	ENSP00000512263.1:p.Arg363Gly
ENST00000695913.1:c.*1843A>G	ENSP00000512264.1:n.*1843A>G
ENST00000695914.1:c.850A>G	ENSP00000512265.1:p.Arg284Gly
ENST00000695918.1:n.318A>G
ENST00000306721.8:c.1090A>G MANE Select	ENSP00000306968.3:p.Arg364Gly
ENST00000306721.7:c.1090A>G	ENSP00000306968.3:p.Arg364Gly
ENST00000347703.7:c.853A>G	ENSP00000272789.4:p.Arg285Gly
ENST00000410019.3:c.727A>G	ENSP00000386833.3:p.Arg243Gly
ENST00000410101.7:c.958A>G	ENSP00000386656.3:p.Arg320Gly
ENST00000467411.5:n.1768+745A>G
ENST00000496441.5:n.1844A>G
NM_031942.4:c.1090A>G	NP_114148.3:p.Arg364Gly
NM_145810.2:c.853A>G	NP_665809.1:p.Arg285Gly
XM_011511957.1:c.1009A>G	XP_011510259.1:p.Arg337Gly
XR_923034.1:n.1988A>G
NM_031942.5:c.1090A>G MANE Select	NP_114148.3:p.Arg364Gly
NM_145810.3:c.853A>G	NP_665809.1:p.Arg285Gly