Canonical Allele Identifier: CA2588120363
Gene: ADAMTS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8600782_8600783del , CM000681.2:g.8600782_8600783del GRCh38
NC_000019.9:g.8665666_8665667del , CM000681.1:g.8665666_8665667del GRCh37
NC_000019.8:g.8571666_8571667del NCBI36
NG_011840.2:g.14920_14921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.810+145_810+146del MANE Select ENSP00000471851.1:n.810+145_810+146del
ENST00000270328.8:c.810+145_810+146del ENSP00000270328.4:n.810+145_810+146del
ENST00000593913.5:c.810+145_810+146del ENSP00000469901.1:n.810+145_810+146del
ENST00000596466.2:n.759+145_759+146del
ENST00000596709.5:n.894+145_894+146del
ENST00000596851.5:c.810+145_810+146del ENSP00000469559.1:n.810+145_810+146del
ENST00000597188.5:c.810+145_810+146del ENSP00000471851.1:n.810+145_810+146del
NM_030957.3:c.810+145_810+146del NP_112219.3:n.810+145_810+146del
XM_006722917.2:c.-300+145_-300+146del XP_006722980.1:n.-300+145_-300+146del
XM_011528331.1:c.810+145_810+146del XP_011526633.1:n.810+145_810+146del
XM_011528332.1:c.810+145_810+146del XP_011526634.1:n.810+145_810+146del
XM_011528333.1:c.810+145_810+146del XP_011526635.1:n.810+145_810+146del
XM_011528334.1:c.810+145_810+146del XP_011526636.1:n.810+145_810+146del
XR_430156.2:n.1086+145_1086+146del
XR_936208.1:n.1086+145_1086+146del
XR_936209.1:n.1086+145_1086+146del
XM_006722917.3:c.-300+145_-300+146del XP_006722980.1:n.-300+145_-300+146del
XM_017027338.2:c.810+145_810+146del XP_016882827.1:n.810+145_810+146del
XR_001753770.1:n.1646+145_1646+146del
NM_030957.4:c.810+145_810+146del MANE Select NP_112219.3:n.810+145_810+146del