Canonical Allele Identifier: CA349330927

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231128G>T (hg19) ; chr2:g.173366400G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366400G>T , CM000664.2:g.173366400G>T	GRCh38
NC_000002.11:g.174231128G>T , CM000664.1:g.174231128G>T	GRCh37
NC_000002.10:g.173939374G>T	NCBI36
NG_047202.1:g.17384G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-750G>T	ENSP00000512251.1:n.799-750G>T
ENST00000695911.1:c.931G>T	ENSP00000512262.1:n.931G>T
ENST00000695912.1:c.1150G>T	ENSP00000512263.1:p.Gly384Cys
ENST00000695913.1:c.*1906G>T	ENSP00000512264.1:n.*1906G>T
ENST00000695914.1:c.913G>T	ENSP00000512265.1:p.Gly305Cys
ENST00000695918.1:n.381G>T
ENST00000306721.8:c.1153G>T MANE Select	ENSP00000306968.3:p.Gly385Cys
ENST00000306721.7:c.1153G>T	ENSP00000306968.3:p.Gly385Cys
ENST00000347703.7:c.916G>T	ENSP00000272789.4:p.Gly306Cys
ENST00000410019.3:c.790G>T	ENSP00000386833.3:p.Gly264Cys
ENST00000410101.7:c.1021G>T	ENSP00000386656.3:p.Gly341Cys
ENST00000467411.5:n.1769-750G>T
ENST00000496441.5:n.1907G>T
NM_031942.4:c.1153G>T	NP_114148.3:p.Gly385Cys
NM_145810.2:c.916G>T	NP_665809.1:p.Gly306Cys
XM_011511957.1:c.1072G>T	XP_011510259.1:p.Gly358Cys
XR_923034.1:n.2051G>T
NM_031942.5:c.1153G>T MANE Select	NP_114148.3:p.Gly385Cys
NM_145810.3:c.916G>T	NP_665809.1:p.Gly306Cys