Canonical Allele Identifier: CA2588116123

Gene: ADAMTS10

Linked Data

• gnomAD v4: 19-8580897-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580899del , CM000681.2:g.8580899del	GRCh38
NC_000019.9:g.8645783del , CM000681.1:g.8645783del	GRCh37
NC_000019.8:g.8551783del	NCBI36
NG_011840.2:g.34805del
NG_052844.1:g.1550del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3307del MANE Select	ENSP00000471851.1:p.His1103ThrfsTer?
ENST00000270328.8:c.3307del	ENSP00000270328.4:p.His1103ThrfsTer?
ENST00000593913.5:c.*2184del	ENSP00000469901.1:n.*2184del
ENST00000595838.5:c.1768del	ENSP00000470501.1:p.His590ThrfsTer?
ENST00000597188.5:c.3307del	ENSP00000471851.1:p.His1103ThrfsTer?
NM_001282352.1:c.1768del	NP_001269281.1:p.His590ThrfsTer?
NM_030957.3:c.3307del	NP_112219.3:p.His1103ThrfsTer?
XM_006722917.2:c.2350del	XP_006722980.1:p.His784ThrfsTer?
XM_011528331.1:c.3454del	XP_011526633.1:p.His1152ThrfsTer?
XM_011528332.1:c.3454del	XP_011526634.1:p.His1152ThrfsTer?
XM_011528333.1:c.3454del	XP_011526635.1:p.His1152ThrfsTer?
XM_011528334.1:c.3130del	XP_011526636.1:p.His1044ThrfsTer?
XM_011528335.1:c.2023del	XP_011526637.1:p.His675ThrfsTer?
XM_011528336.1:c.2017del	XP_011526638.1:p.His673ThrfsTer?
XM_006722917.3:c.2350del	XP_006722980.1:p.His784ThrfsTer?
XM_017027338.2:c.3307del	XP_016882827.1:p.His1103ThrfsTer?
XM_017027339.1:c.1876del	XP_016882828.1:p.His626ThrfsTer?
XM_017027340.1:c.1870del	XP_016882829.1:p.His624ThrfsTer?
NM_030957.4:c.3307del MANE Select	NP_112219.3:p.His1103ThrfsTer?
NM_001282352.2:c.1768del	NP_001269281.1:p.His590ThrfsTer?