Canonical Allele Identifier: CA349330449

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231036A>G (hg19) ; chr2:g.173366308A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366308A>G , CM000664.2:g.173366308A>G	GRCh38
NC_000002.11:g.174231036A>G , CM000664.1:g.174231036A>G	GRCh37
NC_000002.10:g.173939282A>G	NCBI36
NG_047202.1:g.17292A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+716A>G	ENSP00000512251.1:n.798+716A>G
ENST00000695911.1:c.839A>G	ENSP00000512262.1:n.839A>G
ENST00000695912.1:c.1058A>G	ENSP00000512263.1:p.Gln353Arg
ENST00000695913.1:c.*1814A>G	ENSP00000512264.1:n.*1814A>G
ENST00000695914.1:c.821A>G	ENSP00000512265.1:p.Gln274Arg
ENST00000695918.1:n.289A>G
ENST00000306721.8:c.1061A>G MANE Select	ENSP00000306968.3:p.Gln354Arg
ENST00000306721.7:c.1061A>G	ENSP00000306968.3:p.Gln354Arg
ENST00000347703.7:c.824A>G	ENSP00000272789.4:p.Gln275Arg
ENST00000410019.3:c.698A>G	ENSP00000386833.3:p.Gln233Arg
ENST00000410101.7:c.929A>G	ENSP00000386656.3:p.Gln310Arg
ENST00000467411.5:n.1768+716A>G
ENST00000496441.5:n.1815A>G
NM_031942.4:c.1061A>G	NP_114148.3:p.Gln354Arg
NM_145810.2:c.824A>G	NP_665809.1:p.Gln275Arg
XM_011511957.1:c.980A>G	XP_011510259.1:p.Gln327Arg
XR_923034.1:n.1959A>G
NM_031942.5:c.1061A>G MANE Select	NP_114148.3:p.Gln354Arg
NM_145810.3:c.824A>G	NP_665809.1:p.Gln275Arg