Canonical Allele Identifier: CA2556384644
Gene: CCDC40 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80059048_80059053del , CM000679.2:g.80059048_80059053del GRCh38
NC_000017.10:g.78032847_78032852del , CM000679.1:g.78032847_78032852del GRCh37
NC_000017.9:g.75647442_75647447del NCBI36
NG_029761.1:g.27417_27422del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397545.9:c.1440+68_1440+73del MANE Select ENSP00000380679.4:n.1440+68_1440+73del
ENST00000269318.9:c.1440+68_1440+73del ENSP00000269318.5:n.1440+68_1440+73del
ENST00000374876.4:c.1317+397_1317+402del ENSP00000364010.4:n.1317+397_1317+402del
ENST00000374877.7:c.1440+68_1440+73del ENSP00000364011.3:n.1440+68_1440+73del
ENST00000397545.8:c.1440+68_1440+73del ENSP00000380679.4:n.1440+68_1440+73del
ENST00000571028.1:c.56+68_56+73del
ENST00000574799.5:n.977+68_977+73del
NM_001243342.1:c.1440+68_1440+73del NP_001230271.1:n.1440+68_1440+73del
NM_017950.3:c.1440+68_1440+73del NP_060420.2:n.1440+68_1440+73del
XM_005257492.3:c.1440+68_1440+73del XP_005257549.1:n.1440+68_1440+73del
XM_011524963.1:c.1350+68_1350+73del XP_011523265.1:n.1350+68_1350+73del
XM_011524964.1:c.261+68_261+73del XP_011523266.1:n.261+68_261+73del
XM_011524965.1:c.1440+68_1440+73del XP_011523267.1:n.1440+68_1440+73del
XR_934495.1:n.1471+68_1471+73del
NM_001330508.1:c.1440+68_1440+73del NP_001317437.1:n.1440+68_1440+73del
XM_011524963.3:c.1350+68_1350+73del XP_011523265.1:n.1350+68_1350+73del
XM_011524964.3:c.261+68_261+73del XP_011523266.1:n.261+68_261+73del
XM_011524965.3:c.1440+68_1440+73del XP_011523267.1:n.1440+68_1440+73del
XM_017024807.1:c.1440+68_1440+73del XP_016880296.1:n.1440+68_1440+73del
XM_024450821.1:c.1350+68_1350+73del XP_024306589.1:n.1350+68_1350+73del
XR_001752550.2:n.1471+68_1471+73del
XR_934495.2:n.1471+68_1471+73del
NM_017950.4:c.1440+68_1440+73del MANE Select NP_060420.2:n.1440+68_1440+73del
NM_001330508.2:c.1440+68_1440+73del NP_001317437.1:n.1440+68_1440+73del
NM_001243342.2:c.1440+68_1440+73del NP_001230271.1:n.1440+68_1440+73del