Canonical Allele Identifier: CA2321494708
Gene: ADAMTS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8580895A= , CM000681.2:g.8580895A= GRCh38
NC_000019.9:g.8645779A= , CM000681.1:g.8645779A= GRCh37
NC_000019.8:g.8551779A= NCBI36
NG_011840.2:g.34808T=
NG_052844.1:g.1553T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.3310T= MANE Select ENSP00000471851.1:p.Ter1104=
ENST00000270328.8:c.3310T= ENSP00000270328.4:p.Ter1104=
ENST00000593913.5:c.*2187T= ENSP00000469901.1:n.*2187T=
ENST00000595838.5:c.1771T= ENSP00000470501.1:p.Ter591=
ENST00000597188.5:c.3310T= ENSP00000471851.1:p.Ter1104=
NM_001282352.1:c.1771T= NP_001269281.1:p.Ter591=
NM_030957.3:c.3310T= NP_112219.3:p.Ter1104=
XM_006722917.2:c.2353T= XP_006722980.1:p.Ter785=
XM_011528331.1:c.3457T= XP_011526633.1:p.Ter1153=
XM_011528332.1:c.3457T= XP_011526634.1:p.Ter1153=
XM_011528333.1:c.3457T= XP_011526635.1:p.Ter1153=
XM_011528334.1:c.3133T= XP_011526636.1:p.Ter1045=
XM_011528335.1:c.2026T= XP_011526637.1:p.Ter676=
XM_011528336.1:c.2020T= XP_011526638.1:p.Ter674=
XM_006722917.3:c.2353T= XP_006722980.1:p.Ter785=
XM_017027338.2:c.3310T= XP_016882827.1:p.Ter1104=
XM_017027339.1:c.1879T= XP_016882828.1:p.Ter627=
XM_017027340.1:c.1873T= XP_016882829.1:p.Ter625=
NM_030957.4:c.3310T= MANE Select NP_112219.3:p.Ter1104=
NM_001282352.2:c.1771T= NP_001269281.1:p.Ter591=