Canonical Allele Identifier: CA349330812

Gene: CDCA7

Linked Data

• dbSNP Id: rs1465162652
• gnomAD v2: 2-174231105-G-A
• MyVariant Identifiers: chr2:g.174231105G>A (hg19) ; chr2:g.173366377G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366377G>A , CM000664.2:g.173366377G>A	GRCh38
NC_000002.11:g.174231105G>A , CM000664.1:g.174231105G>A	GRCh37
NC_000002.10:g.173939351G>A	NCBI36
NG_047202.1:g.17361G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-773G>A	ENSP00000512251.1:n.799-773G>A
ENST00000695911.1:c.908G>A	ENSP00000512262.1:n.908G>A
ENST00000695912.1:c.1127G>A	ENSP00000512263.1:p.Gly376Asp
ENST00000695913.1:c.*1883G>A	ENSP00000512264.1:n.*1883G>A
ENST00000695914.1:c.890G>A	ENSP00000512265.1:p.Gly297Asp
ENST00000695918.1:n.358G>A
ENST00000306721.8:c.1130G>A MANE Select	ENSP00000306968.3:p.Gly377Asp
ENST00000306721.7:c.1130G>A	ENSP00000306968.3:p.Gly377Asp
ENST00000347703.7:c.893G>A	ENSP00000272789.4:p.Gly298Asp
ENST00000410019.3:c.767G>A	ENSP00000386833.3:p.Gly256Asp
ENST00000410101.7:c.998G>A	ENSP00000386656.3:p.Gly333Asp
ENST00000467411.5:n.1769-773G>A
ENST00000496441.5:n.1884G>A
NM_031942.4:c.1130G>A	NP_114148.3:p.Gly377Asp
NM_145810.2:c.893G>A	NP_665809.1:p.Gly298Asp
XM_011511957.1:c.1049G>A	XP_011510259.1:p.Gly350Asp
XR_923034.1:n.2028G>A
NM_031942.5:c.1130G>A MANE Select	NP_114148.3:p.Gly377Asp
NM_145810.3:c.893G>A	NP_665809.1:p.Gly298Asp