Canonical Allele Identifier: CA2580097152

Gene: ADAMTS10

Linked Data

• ClinVar Variation Id: 2017635
• ClinVar RCV Id: RCV002835276

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580923del , CM000681.2:g.8580923del	GRCh38
NC_000019.9:g.8645807del , CM000681.1:g.8645807del	GRCh37
NC_000019.8:g.8551807del	NCBI36
NG_011840.2:g.34780del
NG_052844.1:g.1525del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3282del MANE Select	ENSP00000471851.1:p.Met1095CysfsTer?
ENST00000270328.8:c.3282del	ENSP00000270328.4:p.Met1095CysfsTer?
ENST00000593913.5:c.*2159del	ENSP00000469901.1:n.*2159del
ENST00000595838.5:c.1743del	ENSP00000470501.1:p.Met582CysfsTer?
ENST00000597188.5:c.3282del	ENSP00000471851.1:p.Met1095CysfsTer?
NM_001282352.1:c.1743del	NP_001269281.1:p.Met582CysfsTer?
NM_030957.3:c.3282del	NP_112219.3:p.Met1095CysfsTer?
XM_006722917.2:c.2325del	XP_006722980.1:p.Met776CysfsTer?
XM_011528331.1:c.3429del	XP_011526633.1:p.Met1144CysfsTer?
XM_011528332.1:c.3429del	XP_011526634.1:p.Met1144CysfsTer?
XM_011528333.1:c.3429del	XP_011526635.1:p.Met1144CysfsTer?
XM_011528334.1:c.3105del	XP_011526636.1:p.Met1036CysfsTer?
XM_011528335.1:c.1998del	XP_011526637.1:p.Met667CysfsTer?
XM_011528336.1:c.1992del	XP_011526638.1:p.Met665CysfsTer?
XM_006722917.3:c.2325del	XP_006722980.1:p.Met776CysfsTer?
XM_017027338.2:c.3282del	XP_016882827.1:p.Met1095CysfsTer?
XM_017027339.1:c.1851del	XP_016882828.1:p.Met618CysfsTer?
XM_017027340.1:c.1845del	XP_016882829.1:p.Met616CysfsTer?
NM_030957.4:c.3282del MANE Select	NP_112219.3:p.Met1095CysfsTer?
NM_001282352.2:c.1743del	NP_001269281.1:p.Met582CysfsTer?