Canonical Allele Identifier: CA349330662

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231075A>T (hg19) ; chr2:g.173366347A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366347A>T , CM000664.2:g.173366347A>T	GRCh38
NC_000002.11:g.174231075A>T , CM000664.1:g.174231075A>T	GRCh37
NC_000002.10:g.173939321A>T	NCBI36
NG_047202.1:g.17331A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+755A>T	ENSP00000512251.1:n.798+755A>T
ENST00000695911.1:c.878A>T	ENSP00000512262.1:n.878A>T
ENST00000695912.1:c.1097A>T	ENSP00000512263.1:p.Asp366Val
ENST00000695913.1:c.*1853A>T	ENSP00000512264.1:n.*1853A>T
ENST00000695914.1:c.860A>T	ENSP00000512265.1:p.Asp287Val
ENST00000695918.1:n.328A>T
ENST00000306721.8:c.1100A>T MANE Select	ENSP00000306968.3:p.Asp367Val
ENST00000306721.7:c.1100A>T	ENSP00000306968.3:p.Asp367Val
ENST00000347703.7:c.863A>T	ENSP00000272789.4:p.Asp288Val
ENST00000410019.3:c.737A>T	ENSP00000386833.3:p.Asp246Val
ENST00000410101.7:c.968A>T	ENSP00000386656.3:p.Asp323Val
ENST00000467411.5:n.1768+755A>T
ENST00000496441.5:n.1854A>T
NM_031942.4:c.1100A>T	NP_114148.3:p.Asp367Val
NM_145810.2:c.863A>T	NP_665809.1:p.Asp288Val
XM_011511957.1:c.1019A>T	XP_011510259.1:p.Asp340Val
XR_923034.1:n.1998A>T
NM_031942.5:c.1100A>T MANE Select	NP_114148.3:p.Asp367Val
NM_145810.3:c.863A>T	NP_665809.1:p.Asp288Val