Canonical Allele Identifier: CA429810512

Gene: CDCA7

Linked Data

• dbSNP Id: rs1686720963
• gnomAD v4: 2-173366388-C-A
• MyVariant Identifiers: chr2:g.174231116C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366388C>A , CM000664.2:g.173366388C>A	GRCh38
NC_000002.11:g.174231116C>A , CM000664.1:g.174231116C>A	GRCh37
NC_000002.10:g.173939362C>A	NCBI36
NG_047202.1:g.17372C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-762C>A	ENSP00000512251.1:n.799-762C>A
ENST00000695911.1:c.919C>A	ENSP00000512262.1:n.919C>A
ENST00000695912.1:c.1138C>A	ENSP00000512263.1:p.Arg380=
ENST00000695913.1:c.*1894C>A	ENSP00000512264.1:n.*1894C>A
ENST00000695914.1:c.901C>A	ENSP00000512265.1:p.Arg301=
ENST00000695918.1:n.369C>A
ENST00000306721.8:c.1141C>A MANE Select	ENSP00000306968.3:p.Arg381=
ENST00000306721.7:c.1141C>A	ENSP00000306968.3:p.Arg381=
ENST00000347703.7:c.904C>A	ENSP00000272789.4:p.Arg302=
ENST00000410019.3:c.778C>A	ENSP00000386833.3:p.Arg260=
ENST00000410101.7:c.1009C>A	ENSP00000386656.3:p.Arg337=
ENST00000467411.5:n.1769-762C>A
ENST00000496441.5:n.1895C>A
NM_031942.4:c.1141C>A	NP_114148.3:p.Arg381=
NM_145810.2:c.904C>A	NP_665809.1:p.Arg302=
XM_011511957.1:c.1060C>A	XP_011510259.1:p.Arg354=
XR_923034.1:n.2039C>A
NM_031942.5:c.1141C>A MANE Select	NP_114148.3:p.Arg381=
NM_145810.3:c.904C>A	NP_665809.1:p.Arg302=