Canonical Allele Identifier: CA349330914

Gene: CDCA7

Linked Data

• gnomAD v4: 2-173366398-A-G
• MyVariant Identifiers: chr2:g.174231126A>G (hg19) ; chr2:g.173366398A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366398A>G , CM000664.2:g.173366398A>G	GRCh38
NC_000002.11:g.174231126A>G , CM000664.1:g.174231126A>G	GRCh37
NC_000002.10:g.173939372A>G	NCBI36
NG_047202.1:g.17382A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-752A>G	ENSP00000512251.1:n.799-752A>G
ENST00000695911.1:c.929A>G	ENSP00000512262.1:n.929A>G
ENST00000695912.1:c.1148A>G	ENSP00000512263.1:p.Tyr383Cys
ENST00000695913.1:c.*1904A>G	ENSP00000512264.1:n.*1904A>G
ENST00000695914.1:c.911A>G	ENSP00000512265.1:p.Tyr304Cys
ENST00000695918.1:n.379A>G
ENST00000306721.8:c.1151A>G MANE Select	ENSP00000306968.3:p.Tyr384Cys
ENST00000306721.7:c.1151A>G	ENSP00000306968.3:p.Tyr384Cys
ENST00000347703.7:c.914A>G	ENSP00000272789.4:p.Tyr305Cys
ENST00000410019.3:c.788A>G	ENSP00000386833.3:p.Tyr263Cys
ENST00000410101.7:c.1019A>G	ENSP00000386656.3:p.Tyr340Cys
ENST00000467411.5:n.1769-752A>G
ENST00000496441.5:n.1905A>G
NM_031942.4:c.1151A>G	NP_114148.3:p.Tyr384Cys
NM_145810.2:c.914A>G	NP_665809.1:p.Tyr305Cys
XM_011511957.1:c.1070A>G	XP_011510259.1:p.Tyr357Cys
XR_923034.1:n.2049A>G
NM_031942.5:c.1151A>G MANE Select	NP_114148.3:p.Tyr384Cys
NM_145810.3:c.914A>G	NP_665809.1:p.Tyr305Cys