Canonical Allele Identifier: CA349330722

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366361-C-G
• MyVariant Identifiers: chr2:g.174231089C>G (hg19) ; chr2:g.173366361C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366361C>G , CM000664.2:g.173366361C>G	GRCh38
NC_000002.11:g.174231089C>G , CM000664.1:g.174231089C>G	GRCh37
NC_000002.10:g.173939335C>G	NCBI36
NG_047202.1:g.17345C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+769C>G	ENSP00000512251.1:n.798+769C>G
ENST00000695911.1:c.892C>G	ENSP00000512262.1:n.892C>G
ENST00000695912.1:c.1111C>G	ENSP00000512263.1:p.Arg371Gly
ENST00000695913.1:c.*1867C>G	ENSP00000512264.1:n.*1867C>G
ENST00000695914.1:c.874C>G	ENSP00000512265.1:p.Arg292Gly
ENST00000695918.1:n.342C>G
ENST00000306721.8:c.1114C>G MANE Select	ENSP00000306968.3:p.Arg372Gly
ENST00000306721.7:c.1114C>G	ENSP00000306968.3:p.Arg372Gly
ENST00000347703.7:c.877C>G	ENSP00000272789.4:p.Arg293Gly
ENST00000410019.3:c.751C>G	ENSP00000386833.3:p.Arg251Gly
ENST00000410101.7:c.982C>G	ENSP00000386656.3:p.Arg328Gly
ENST00000467411.5:n.1768+769C>G
ENST00000496441.5:n.1868C>G
NM_031942.4:c.1114C>G	NP_114148.3:p.Arg372Gly
NM_145810.2:c.877C>G	NP_665809.1:p.Arg293Gly
XM_011511957.1:c.1033C>G	XP_011510259.1:p.Arg345Gly
XR_923034.1:n.2012C>G
NM_031942.5:c.1114C>G MANE Select	NP_114148.3:p.Arg372Gly
NM_145810.3:c.877C>G	NP_665809.1:p.Arg293Gly