Canonical Allele Identifier: CA349331062

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231152C>A (hg19) ; chr2:g.173366424C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366424C>A , CM000664.2:g.173366424C>A	GRCh38
NC_000002.11:g.174231152C>A , CM000664.1:g.174231152C>A	GRCh37
NC_000002.10:g.173939398C>A	NCBI36
NG_047202.1:g.17408C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-726C>A	ENSP00000512251.1:n.799-726C>A
ENST00000695911.1:c.955C>A	ENSP00000512262.1:n.955C>A
ENST00000695912.1:c.1174C>A	ENSP00000512263.1:p.Leu392Met
ENST00000695913.1:c.*1930C>A	ENSP00000512264.1:n.*1930C>A
ENST00000695914.1:c.937C>A	ENSP00000512265.1:p.Leu313Met
ENST00000695918.1:n.405C>A
ENST00000306721.8:c.1177C>A MANE Select	ENSP00000306968.3:p.Leu393Met
ENST00000306721.7:c.1177C>A	ENSP00000306968.3:p.Leu393Met
ENST00000347703.7:c.940C>A	ENSP00000272789.4:p.Leu314Met
ENST00000410019.3:c.814C>A	ENSP00000386833.3:p.Leu272Met
ENST00000410101.7:c.1045C>A	ENSP00000386656.3:p.Leu349Met
ENST00000467411.5:n.1769-726C>A
ENST00000496441.5:n.1931C>A
NM_031942.4:c.1177C>A	NP_114148.3:p.Leu393Met
NM_145810.2:c.940C>A	NP_665809.1:p.Leu314Met
XM_011511957.1:c.1096C>A	XP_011510259.1:p.Leu366Met
XR_923034.1:n.2075C>A
NM_031942.5:c.1177C>A MANE Select	NP_114148.3:p.Leu393Met
NM_145810.3:c.940C>A	NP_665809.1:p.Leu314Met