Canonical Allele Identifier: CA2588120939
Gene: ADAMTS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8604955_8604956del , CM000681.2:g.8604955_8604956del GRCh38
NC_000019.9:g.8669840_8669841del , CM000681.1:g.8669840_8669841del GRCh37
NC_000019.8:g.8575840_8575841del NCBI36
NG_011840.2:g.10750_10751del

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.435+59_435+60del MANE Select ENSP00000471851.1:n.435+59_435+60del
ENST00000270328.8:c.435+59_435+60del ENSP00000270328.4:n.435+59_435+60del
ENST00000593534.1:n.613_614del
ENST00000593913.5:c.435+59_435+60del ENSP00000469901.1:n.435+59_435+60del
ENST00000596466.2:n.384+59_384+60del
ENST00000596709.5:n.519+59_519+60del
ENST00000596851.5:c.435+59_435+60del ENSP00000469559.1:n.435+59_435+60del
ENST00000597188.5:c.435+59_435+60del ENSP00000471851.1:n.435+59_435+60del
NM_030957.3:c.435+59_435+60del NP_112219.3:n.435+59_435+60del
XM_006722917.2:c.-675+59_-675+60del XP_006722980.1:n.-675+59_-675+60del
XM_011528331.1:c.435+59_435+60del XP_011526633.1:n.435+59_435+60del
XM_011528332.1:c.435+59_435+60del XP_011526634.1:n.435+59_435+60del
XM_011528333.1:c.435+59_435+60del XP_011526635.1:n.435+59_435+60del
XM_011528334.1:c.435+59_435+60del XP_011526636.1:n.435+59_435+60del
XR_430156.2:n.711+59_711+60del
XR_936208.1:n.711+59_711+60del
XR_936209.1:n.711+59_711+60del
XM_006722917.3:c.-675+59_-675+60del XP_006722980.1:n.-675+59_-675+60del
XM_017027338.2:c.435+59_435+60del XP_016882827.1:n.435+59_435+60del
XR_001753770.1:n.1271+59_1271+60del
NM_030957.4:c.435+59_435+60del MANE Select NP_112219.3:n.435+59_435+60del