Canonical Allele Identifier: CA349330809

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231104G>T (hg19) ; chr2:g.173366376G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366376G>T , CM000664.2:g.173366376G>T	GRCh38
NC_000002.11:g.174231104G>T , CM000664.1:g.174231104G>T	GRCh37
NC_000002.10:g.173939350G>T	NCBI36
NG_047202.1:g.17360G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-774G>T	ENSP00000512251.1:n.799-774G>T
ENST00000695911.1:c.907G>T	ENSP00000512262.1:n.907G>T
ENST00000695912.1:c.1126G>T	ENSP00000512263.1:p.Gly376Cys
ENST00000695913.1:c.*1882G>T	ENSP00000512264.1:n.*1882G>T
ENST00000695914.1:c.889G>T	ENSP00000512265.1:p.Gly297Cys
ENST00000695918.1:n.357G>T
ENST00000306721.8:c.1129G>T MANE Select	ENSP00000306968.3:p.Gly377Cys
ENST00000306721.7:c.1129G>T	ENSP00000306968.3:p.Gly377Cys
ENST00000347703.7:c.892G>T	ENSP00000272789.4:p.Gly298Cys
ENST00000410019.3:c.766G>T	ENSP00000386833.3:p.Gly256Cys
ENST00000410101.7:c.997G>T	ENSP00000386656.3:p.Gly333Cys
ENST00000467411.5:n.1769-774G>T
ENST00000496441.5:n.1883G>T
NM_031942.4:c.1129G>T	NP_114148.3:p.Gly377Cys
NM_145810.2:c.892G>T	NP_665809.1:p.Gly298Cys
XM_011511957.1:c.1048G>T	XP_011510259.1:p.Gly350Cys
XR_923034.1:n.2027G>T
NM_031942.5:c.1129G>T MANE Select	NP_114148.3:p.Gly377Cys
NM_145810.3:c.892G>T	NP_665809.1:p.Gly298Cys