Canonical Allele Identifier: CA349330822

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231108C>A (hg19) ; chr2:g.173366380C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366380C>A , CM000664.2:g.173366380C>A	GRCh38
NC_000002.11:g.174231108C>A , CM000664.1:g.174231108C>A	GRCh37
NC_000002.10:g.173939354C>A	NCBI36
NG_047202.1:g.17364C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-770C>A	ENSP00000512251.1:n.799-770C>A
ENST00000695911.1:c.911C>A	ENSP00000512262.1:n.911C>A
ENST00000695912.1:c.1130C>A	ENSP00000512263.1:p.Pro377His
ENST00000695913.1:c.*1886C>A	ENSP00000512264.1:n.*1886C>A
ENST00000695914.1:c.893C>A	ENSP00000512265.1:p.Pro298His
ENST00000695918.1:n.361C>A
ENST00000306721.8:c.1133C>A MANE Select	ENSP00000306968.3:p.Pro378His
ENST00000306721.7:c.1133C>A	ENSP00000306968.3:p.Pro378His
ENST00000347703.7:c.896C>A	ENSP00000272789.4:p.Pro299His
ENST00000410019.3:c.770C>A	ENSP00000386833.3:p.Pro257His
ENST00000410101.7:c.1001C>A	ENSP00000386656.3:p.Pro334His
ENST00000467411.5:n.1769-770C>A
ENST00000496441.5:n.1887C>A
NM_031942.4:c.1133C>A	NP_114148.3:p.Pro378His
NM_145810.2:c.896C>A	NP_665809.1:p.Pro299His
XM_011511957.1:c.1052C>A	XP_011510259.1:p.Pro351His
XR_923034.1:n.2031C>A
NM_031942.5:c.1133C>A MANE Select	NP_114148.3:p.Pro378His
NM_145810.3:c.896C>A	NP_665809.1:p.Pro299His