Canonical Allele Identifier: CA349330427

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231032C>G (hg19) ; chr2:g.173366304C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366304C>G , CM000664.2:g.173366304C>G	GRCh38
NC_000002.11:g.174231032C>G , CM000664.1:g.174231032C>G	GRCh37
NC_000002.10:g.173939278C>G	NCBI36
NG_047202.1:g.17288C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+712C>G	ENSP00000512251.1:n.798+712C>G
ENST00000695911.1:c.835C>G	ENSP00000512262.1:n.835C>G
ENST00000695912.1:c.1054C>G	ENSP00000512263.1:p.Arg352Gly
ENST00000695913.1:c.*1810C>G	ENSP00000512264.1:n.*1810C>G
ENST00000695914.1:c.817C>G	ENSP00000512265.1:p.Arg273Gly
ENST00000695918.1:n.285C>G
ENST00000306721.8:c.1057C>G MANE Select	ENSP00000306968.3:p.Arg353Gly
ENST00000306721.7:c.1057C>G	ENSP00000306968.3:p.Arg353Gly
ENST00000347703.7:c.820C>G	ENSP00000272789.4:p.Arg274Gly
ENST00000410019.3:c.694C>G	ENSP00000386833.3:p.Arg232Gly
ENST00000410101.7:c.925C>G	ENSP00000386656.3:p.Arg309Gly
ENST00000467411.5:n.1768+712C>G
ENST00000496441.5:n.1811C>G
NM_031942.4:c.1057C>G	NP_114148.3:p.Arg353Gly
NM_145810.2:c.820C>G	NP_665809.1:p.Arg274Gly
XM_011511957.1:c.976C>G	XP_011510259.1:p.Arg326Gly
XR_923034.1:n.1955C>G
NM_031942.5:c.1057C>G MANE Select	NP_114148.3:p.Arg353Gly
NM_145810.3:c.820C>G	NP_665809.1:p.Arg274Gly