Canonical Allele Identifier: CA349330413

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231029T>G (hg19) ; chr2:g.173366301T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366301T>G , CM000664.2:g.173366301T>G	GRCh38
NC_000002.11:g.174231029T>G , CM000664.1:g.174231029T>G	GRCh37
NC_000002.10:g.173939275T>G	NCBI36
NG_047202.1:g.17285T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+709T>G	ENSP00000512251.1:n.798+709T>G
ENST00000695911.1:c.832T>G	ENSP00000512262.1:n.832T>G
ENST00000695912.1:c.1051T>G	ENSP00000512263.1:p.Cys351Gly
ENST00000695913.1:c.*1807T>G	ENSP00000512264.1:n.*1807T>G
ENST00000695914.1:c.814T>G	ENSP00000512265.1:p.Cys272Gly
ENST00000695918.1:n.282T>G
ENST00000306721.8:c.1054T>G MANE Select	ENSP00000306968.3:p.Cys352Gly
ENST00000306721.7:c.1054T>G	ENSP00000306968.3:p.Cys352Gly
ENST00000347703.7:c.817T>G	ENSP00000272789.4:p.Cys273Gly
ENST00000410019.3:c.691T>G	ENSP00000386833.3:p.Cys231Gly
ENST00000410101.7:c.922T>G	ENSP00000386656.3:p.Cys308Gly
ENST00000467411.5:n.1768+709T>G
ENST00000496441.5:n.1808T>G
NM_031942.4:c.1054T>G	NP_114148.3:p.Cys352Gly
NM_145810.2:c.817T>G	NP_665809.1:p.Cys273Gly
XM_011511957.1:c.973T>G	XP_011510259.1:p.Cys325Gly
XR_923034.1:n.1952T>G
NM_031942.5:c.1054T>G MANE Select	NP_114148.3:p.Cys352Gly
NM_145810.3:c.817T>G	NP_665809.1:p.Cys273Gly