Canonical Allele Identifier: CA349330689

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231081G>A (hg19) ; chr2:g.173366353G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366353G>A , CM000664.2:g.173366353G>A	GRCh38
NC_000002.11:g.174231081G>A , CM000664.1:g.174231081G>A	GRCh37
NC_000002.10:g.173939327G>A	NCBI36
NG_047202.1:g.17337G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+761G>A	ENSP00000512251.1:n.798+761G>A
ENST00000695911.1:c.884G>A	ENSP00000512262.1:n.884G>A
ENST00000695912.1:c.1103G>A	ENSP00000512263.1:p.Trp368Ter
ENST00000695913.1:c.*1859G>A	ENSP00000512264.1:n.*1859G>A
ENST00000695914.1:c.866G>A	ENSP00000512265.1:p.Trp289Ter
ENST00000695918.1:n.334G>A
ENST00000306721.8:c.1106G>A MANE Select	ENSP00000306968.3:p.Trp369Ter
ENST00000306721.7:c.1106G>A	ENSP00000306968.3:p.Trp369Ter
ENST00000347703.7:c.869G>A	ENSP00000272789.4:p.Trp290Ter
ENST00000410019.3:c.743G>A	ENSP00000386833.3:p.Trp248Ter
ENST00000410101.7:c.974G>A	ENSP00000386656.3:p.Trp325Ter
ENST00000467411.5:n.1768+761G>A
ENST00000496441.5:n.1860G>A
NM_031942.4:c.1106G>A	NP_114148.3:p.Trp369Ter
NM_145810.2:c.869G>A	NP_665809.1:p.Trp290Ter
XM_011511957.1:c.1025G>A	XP_011510259.1:p.Trp342Ter
XR_923034.1:n.2004G>A
NM_031942.5:c.1106G>A MANE Select	NP_114148.3:p.Trp369Ter
NM_145810.3:c.869G>A	NP_665809.1:p.Trp290Ter