Canonical Allele Identifier: CA349330752

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231095C>G (hg19) ; chr2:g.173366367C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366367C>G , CM000664.2:g.173366367C>G	GRCh38
NC_000002.11:g.174231095C>G , CM000664.1:g.174231095C>G	GRCh37
NC_000002.10:g.173939341C>G	NCBI36
NG_047202.1:g.17351C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695901.1:c.798+775C>G	ENSP00000512251.1:n.798+775C>G
ENST00000695911.1:c.898C>G	ENSP00000512262.1:n.898C>G
ENST00000695912.1:c.1117C>G	ENSP00000512263.1:p.Gln373Glu
ENST00000695913.1:c.*1873C>G	ENSP00000512264.1:n.*1873C>G
ENST00000695914.1:c.880C>G	ENSP00000512265.1:p.Gln294Glu
ENST00000695918.1:n.348C>G
ENST00000306721.8:c.1120C>G MANE Select	ENSP00000306968.3:p.Gln374Glu
ENST00000306721.7:c.1120C>G	ENSP00000306968.3:p.Gln374Glu
ENST00000347703.7:c.883C>G	ENSP00000272789.4:p.Gln295Glu
ENST00000410019.3:c.757C>G	ENSP00000386833.3:p.Gln253Glu
ENST00000410101.7:c.988C>G	ENSP00000386656.3:p.Gln330Glu
ENST00000467411.5:n.1768+775C>G
ENST00000496441.5:n.1874C>G
NM_031942.4:c.1120C>G	NP_114148.3:p.Gln374Glu
NM_145810.2:c.883C>G	NP_665809.1:p.Gln295Glu
XM_011511957.1:c.1039C>G	XP_011510259.1:p.Gln347Glu
XR_923034.1:n.2018C>G
NM_031942.5:c.1120C>G MANE Select	NP_114148.3:p.Gln374Glu
NM_145810.3:c.883C>G	NP_665809.1:p.Gln295Glu