Canonical Allele Identifier: CA2321494726
Gene: ADAMTS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8580951T= , CM000681.2:g.8580951T= GRCh38
NC_000019.9:g.8645835T= , CM000681.1:g.8645835T= GRCh37
NC_000019.8:g.8551835T= NCBI36
NG_011840.2:g.34752A=
NG_052844.1:g.1497A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.3254A= MANE Select ENSP00000471851.1:p.Gln1085=
ENST00000270328.8:c.3254A= ENSP00000270328.4:p.Gln1085=
ENST00000593913.5:c.*2131A= ENSP00000469901.1:n.*2131A=
ENST00000595838.5:c.1715A= ENSP00000470501.1:p.Gln572=
ENST00000597188.5:c.3254A= ENSP00000471851.1:p.Gln1085=
NM_001282352.1:c.1715A= NP_001269281.1:p.Gln572=
NM_030957.3:c.3254A= NP_112219.3:p.Gln1085=
XM_006722917.2:c.2297A= XP_006722980.1:p.Gln766=
XM_011528331.1:c.3401A= XP_011526633.1:p.Gln1134=
XM_011528332.1:c.3401A= XP_011526634.1:p.Gln1134=
XM_011528333.1:c.3401A= XP_011526635.1:p.Gln1134=
XM_011528334.1:c.3077A= XP_011526636.1:p.Gln1026=
XM_011528335.1:c.1970A= XP_011526637.1:p.Gln657=
XM_011528336.1:c.1964A= XP_011526638.1:p.Gln655=
XM_006722917.3:c.2297A= XP_006722980.1:p.Gln766=
XM_017027338.2:c.3254A= XP_016882827.1:p.Gln1085=
XM_017027339.1:c.1823A= XP_016882828.1:p.Gln608=
XM_017027340.1:c.1817A= XP_016882829.1:p.Gln606=
NM_030957.4:c.3254A= MANE Select NP_112219.3:p.Gln1085=
NM_001282352.2:c.1715A= NP_001269281.1:p.Gln572=