Canonical Allele Identifier: CA349330735

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231092G>A (hg19) ; chr2:g.173366364G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366364G>A , CM000664.2:g.173366364G>A	GRCh38
NC_000002.11:g.174231092G>A , CM000664.1:g.174231092G>A	GRCh37
NC_000002.10:g.173939338G>A	NCBI36
NG_047202.1:g.17348G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+772G>A	ENSP00000512251.1:n.798+772G>A
ENST00000695911.1:c.895G>A	ENSP00000512262.1:n.895G>A
ENST00000695912.1:c.1114G>A	ENSP00000512263.1:p.Gly372Ser
ENST00000695913.1:c.*1870G>A	ENSP00000512264.1:n.*1870G>A
ENST00000695914.1:c.877G>A	ENSP00000512265.1:p.Gly293Ser
ENST00000695918.1:n.345G>A
ENST00000306721.8:c.1117G>A MANE Select	ENSP00000306968.3:p.Gly373Ser
ENST00000306721.7:c.1117G>A	ENSP00000306968.3:p.Gly373Ser
ENST00000347703.7:c.880G>A	ENSP00000272789.4:p.Gly294Ser
ENST00000410019.3:c.754G>A	ENSP00000386833.3:p.Gly252Ser
ENST00000410101.7:c.985G>A	ENSP00000386656.3:p.Gly329Ser
ENST00000467411.5:n.1768+772G>A
ENST00000496441.5:n.1871G>A
NM_031942.4:c.1117G>A	NP_114148.3:p.Gly373Ser
NM_145810.2:c.880G>A	NP_665809.1:p.Gly294Ser
XM_011511957.1:c.1036G>A	XP_011510259.1:p.Gly346Ser
XR_923034.1:n.2015G>A
NM_031942.5:c.1117G>A MANE Select	NP_114148.3:p.Gly373Ser
NM_145810.3:c.880G>A	NP_665809.1:p.Gly294Ser