Canonical Allele Identifier: CA349330475

Gene: CDCA7

Linked Data

• dbSNP Id: rs1686719440
• gnomAD v4: 2-173366316-A-G
• MyVariant Identifiers: chr2:g.174231044A>G (hg19) ; chr2:g.173366316A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366316A>G , CM000664.2:g.173366316A>G	GRCh38
NC_000002.11:g.174231044A>G , CM000664.1:g.174231044A>G	GRCh37
NC_000002.10:g.173939290A>G	NCBI36
NG_047202.1:g.17300A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+724A>G	ENSP00000512251.1:n.798+724A>G
ENST00000695911.1:c.847A>G	ENSP00000512262.1:n.847A>G
ENST00000695912.1:c.1066A>G	ENSP00000512263.1:p.Ile356Val
ENST00000695913.1:c.*1822A>G	ENSP00000512264.1:n.*1822A>G
ENST00000695914.1:c.829A>G	ENSP00000512265.1:p.Ile277Val
ENST00000695918.1:n.297A>G
ENST00000306721.8:c.1069A>G MANE Select	ENSP00000306968.3:p.Ile357Val
ENST00000306721.7:c.1069A>G	ENSP00000306968.3:p.Ile357Val
ENST00000347703.7:c.832A>G	ENSP00000272789.4:p.Ile278Val
ENST00000410019.3:c.706A>G	ENSP00000386833.3:p.Ile236Val
ENST00000410101.7:c.937A>G	ENSP00000386656.3:p.Ile313Val
ENST00000467411.5:n.1768+724A>G
ENST00000496441.5:n.1823A>G
NM_031942.4:c.1069A>G	NP_114148.3:p.Ile357Val
NM_145810.2:c.832A>G	NP_665809.1:p.Ile278Val
XM_011511957.1:c.988A>G	XP_011510259.1:p.Ile330Val
XR_923034.1:n.1967A>G
NM_031942.5:c.1069A>G MANE Select	NP_114148.3:p.Ile357Val
NM_145810.3:c.832A>G	NP_665809.1:p.Ile278Val