Canonical Allele Identifier: CA349330890

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231122C>G (hg19) ; chr2:g.173366394C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366394C>G , CM000664.2:g.173366394C>G	GRCh38
NC_000002.11:g.174231122C>G , CM000664.1:g.174231122C>G	GRCh37
NC_000002.10:g.173939368C>G	NCBI36
NG_047202.1:g.17378C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-756C>G	ENSP00000512251.1:n.799-756C>G
ENST00000695911.1:c.925C>G	ENSP00000512262.1:n.925C>G
ENST00000695912.1:c.1144C>G	ENSP00000512263.1:p.Arg382Gly
ENST00000695913.1:c.*1900C>G	ENSP00000512264.1:n.*1900C>G
ENST00000695914.1:c.907C>G	ENSP00000512265.1:p.Arg303Gly
ENST00000695918.1:n.375C>G
ENST00000306721.8:c.1147C>G MANE Select	ENSP00000306968.3:p.Arg383Gly
ENST00000306721.7:c.1147C>G	ENSP00000306968.3:p.Arg383Gly
ENST00000347703.7:c.910C>G	ENSP00000272789.4:p.Arg304Gly
ENST00000410019.3:c.784C>G	ENSP00000386833.3:p.Arg262Gly
ENST00000410101.7:c.1015C>G	ENSP00000386656.3:p.Arg339Gly
ENST00000467411.5:n.1769-756C>G
ENST00000496441.5:n.1901C>G
NM_031942.4:c.1147C>G	NP_114148.3:p.Arg383Gly
NM_145810.2:c.910C>G	NP_665809.1:p.Arg304Gly
XM_011511957.1:c.1066C>G	XP_011510259.1:p.Arg356Gly
XR_923034.1:n.2045C>G
NM_031942.5:c.1147C>G MANE Select	NP_114148.3:p.Arg383Gly
NM_145810.3:c.910C>G	NP_665809.1:p.Arg304Gly