Canonical Allele Identifier: CA349330526

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231054A>G (hg19) ; chr2:g.173366326A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366326A>G , CM000664.2:g.173366326A>G	GRCh38
NC_000002.11:g.174231054A>G , CM000664.1:g.174231054A>G	GRCh37
NC_000002.10:g.173939300A>G	NCBI36
NG_047202.1:g.17310A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+734A>G	ENSP00000512251.1:n.798+734A>G
ENST00000695911.1:c.857A>G	ENSP00000512262.1:n.857A>G
ENST00000695912.1:c.1076A>G	ENSP00000512263.1:p.Lys359Arg
ENST00000695913.1:c.*1832A>G	ENSP00000512264.1:n.*1832A>G
ENST00000695914.1:c.839A>G	ENSP00000512265.1:p.Lys280Arg
ENST00000695918.1:n.307A>G
ENST00000306721.8:c.1079A>G MANE Select	ENSP00000306968.3:p.Lys360Arg
ENST00000306721.7:c.1079A>G	ENSP00000306968.3:p.Lys360Arg
ENST00000347703.7:c.842A>G	ENSP00000272789.4:p.Lys281Arg
ENST00000410019.3:c.716A>G	ENSP00000386833.3:p.Lys239Arg
ENST00000410101.7:c.947A>G	ENSP00000386656.3:p.Lys316Arg
ENST00000467411.5:n.1768+734A>G
ENST00000496441.5:n.1833A>G
NM_031942.4:c.1079A>G	NP_114148.3:p.Lys360Arg
NM_145810.2:c.842A>G	NP_665809.1:p.Lys281Arg
XM_011511957.1:c.998A>G	XP_011510259.1:p.Lys333Arg
XR_923034.1:n.1977A>G
NM_031942.5:c.1079A>G MANE Select	NP_114148.3:p.Lys360Arg
NM_145810.3:c.842A>G	NP_665809.1:p.Lys281Arg