Canonical Allele Identifier: CA2661982939
Gene: CDCA7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.173366206_173366207del , CM000664.2:g.173366206_173366207del GRCh38
NC_000002.11:g.174230934_174230935del , CM000664.1:g.174230934_174230935del GRCh37
NC_000002.10:g.173939180_173939181del NCBI36
NG_047202.1:g.17190_17191del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695901.1:c.798+614_798+615del ENSP00000512251.1:n.798+614_798+615del
ENST00000695911.1:c.814-77_814-76del ENSP00000512262.1:n.814-77_814-76del
ENST00000695912.1:c.1033-77_1033-76del ENSP00000512263.1:n.1033-77_1033-76del
ENST00000695913.1:c.*1712_*1713del ENSP00000512264.1:n.*1712_*1713del
ENST00000695914.1:c.796-77_796-76del ENSP00000512265.1:n.796-77_796-76del
ENST00000695918.1:n.264-77_264-76del
ENST00000306721.8:c.1036-77_1036-76del MANE Select ENSP00000306968.3:n.1036-77_1036-76del
ENST00000306721.7:c.1036-77_1036-76del ENSP00000306968.3:n.1036-77_1036-76del
ENST00000347703.7:c.799-77_799-76del ENSP00000272789.4:n.799-77_799-76del
ENST00000410019.3:c.673-77_673-76del ENSP00000386833.3:n.673-77_673-76del
ENST00000410101.7:c.904-77_904-76del ENSP00000386656.3:n.904-77_904-76del
ENST00000467411.5:n.1768+614_1768+615del
ENST00000496441.5:n.1790-77_1790-76del
NM_031942.4:c.1036-77_1036-76del NP_114148.3:n.1036-77_1036-76del
NM_145810.2:c.799-77_799-76del NP_665809.1:n.799-77_799-76del
XM_011511957.1:c.955-77_955-76del XP_011510259.1:n.955-77_955-76del
XR_923034.1:n.1934-77_1934-76del
NM_031942.5:c.1036-77_1036-76del MANE Select NP_114148.3:n.1036-77_1036-76del
NM_145810.3:c.799-77_799-76del NP_665809.1:n.799-77_799-76del