Canonical Allele Identifier: CA349330816

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366377-G-T
• MyVariant Identifiers: chr2:g.174231105G>T (hg19) ; chr2:g.173366377G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-773G>T	ENSP00000512251.1:n.799-773G>T
ENST00000695911.1:c.908G>T	ENSP00000512262.1:n.908G>T
ENST00000695912.1:c.1127G>T	ENSP00000512263.1:p.Gly376Val
ENST00000695913.1:c.*1883G>T	ENSP00000512264.1:n.*1883G>T
ENST00000695914.1:c.890G>T	ENSP00000512265.1:p.Gly297Val
ENST00000695918.1:n.358G>T
ENST00000306721.8:c.1130G>T MANE Select	ENSP00000306968.3:p.Gly377Val
ENST00000306721.7:c.1130G>T	ENSP00000306968.3:p.Gly377Val
ENST00000347703.7:c.893G>T	ENSP00000272789.4:p.Gly298Val
ENST00000410019.3:c.767G>T	ENSP00000386833.3:p.Gly256Val
ENST00000410101.7:c.998G>T	ENSP00000386656.3:p.Gly333Val
ENST00000467411.5:n.1769-773G>T
ENST00000496441.5:n.1884G>T
NM_031942.4:c.1130G>T	NP_114148.3:p.Gly377Val
NM_145810.2:c.893G>T	NP_665809.1:p.Gly298Val
XM_011511957.1:c.1049G>T	XP_011510259.1:p.Gly350Val
XR_923034.1:n.2028G>T
NM_031942.5:c.1130G>T MANE Select	NP_114148.3:p.Gly377Val
NM_145810.3:c.893G>T	NP_665809.1:p.Gly298Val