Canonical Allele Identifier: CA349330686

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231080T>G (hg19) ; chr2:g.173366352T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366352T>G , CM000664.2:g.173366352T>G	GRCh38
NC_000002.11:g.174231080T>G , CM000664.1:g.174231080T>G	GRCh37
NC_000002.10:g.173939326T>G	NCBI36
NG_047202.1:g.17336T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+760T>G	ENSP00000512251.1:n.798+760T>G
ENST00000695911.1:c.883T>G	ENSP00000512262.1:n.883T>G
ENST00000695912.1:c.1102T>G	ENSP00000512263.1:p.Trp368Gly
ENST00000695913.1:c.*1858T>G	ENSP00000512264.1:n.*1858T>G
ENST00000695914.1:c.865T>G	ENSP00000512265.1:p.Trp289Gly
ENST00000695918.1:n.333T>G
ENST00000306721.8:c.1105T>G MANE Select	ENSP00000306968.3:p.Trp369Gly
ENST00000306721.7:c.1105T>G	ENSP00000306968.3:p.Trp369Gly
ENST00000347703.7:c.868T>G	ENSP00000272789.4:p.Trp290Gly
ENST00000410019.3:c.742T>G	ENSP00000386833.3:p.Trp248Gly
ENST00000410101.7:c.973T>G	ENSP00000386656.3:p.Trp325Gly
ENST00000467411.5:n.1768+760T>G
ENST00000496441.5:n.1859T>G
NM_031942.4:c.1105T>G	NP_114148.3:p.Trp369Gly
NM_145810.2:c.868T>G	NP_665809.1:p.Trp290Gly
XM_011511957.1:c.1024T>G	XP_011510259.1:p.Trp342Gly
XR_923034.1:n.2003T>G
NM_031942.5:c.1105T>G MANE Select	NP_114148.3:p.Trp369Gly
NM_145810.3:c.868T>G	NP_665809.1:p.Trp290Gly