Canonical Allele Identifier: CA349330707

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231084G>T (hg19) ; chr2:g.173366356G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366356G>T , CM000664.2:g.173366356G>T	GRCh38
NC_000002.11:g.174231084G>T , CM000664.1:g.174231084G>T	GRCh37
NC_000002.10:g.173939330G>T	NCBI36
NG_047202.1:g.17340G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+764G>T	ENSP00000512251.1:n.798+764G>T
ENST00000695911.1:c.887G>T	ENSP00000512262.1:n.887G>T
ENST00000695912.1:c.1106G>T	ENSP00000512263.1:p.Gly369Val
ENST00000695913.1:c.*1862G>T	ENSP00000512264.1:n.*1862G>T
ENST00000695914.1:c.869G>T	ENSP00000512265.1:p.Gly290Val
ENST00000695918.1:n.337G>T
ENST00000306721.8:c.1109G>T MANE Select	ENSP00000306968.3:p.Gly370Val
ENST00000306721.7:c.1109G>T	ENSP00000306968.3:p.Gly370Val
ENST00000347703.7:c.872G>T	ENSP00000272789.4:p.Gly291Val
ENST00000410019.3:c.746G>T	ENSP00000386833.3:p.Gly249Val
ENST00000410101.7:c.977G>T	ENSP00000386656.3:p.Gly326Val
ENST00000467411.5:n.1768+764G>T
ENST00000496441.5:n.1863G>T
NM_031942.4:c.1109G>T	NP_114148.3:p.Gly370Val
NM_145810.2:c.872G>T	NP_665809.1:p.Gly291Val
XM_011511957.1:c.1028G>T	XP_011510259.1:p.Gly343Val
XR_923034.1:n.2007G>T
NM_031942.5:c.1109G>T MANE Select	NP_114148.3:p.Gly370Val
NM_145810.3:c.872G>T	NP_665809.1:p.Gly291Val