Canonical Allele Identifier: CA2321496525
Gene: ADAMTS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8584907C= , CM000681.2:g.8584907C= GRCh38
NC_000019.9:g.8649791C= , CM000681.1:g.8649791C= GRCh37
NC_000019.8:g.8555791C= NCBI36
NG_011840.2:g.30796G=

Transcript Alleles

HGVS Amino-acid change
ENST00000597188.6:c.3190G= MANE Select ENSP00000471851.1:p.Asp1064=
ENST00000270328.8:c.3190G= ENSP00000270328.4:p.Asp1064=
ENST00000593913.5:c.*2067G= ENSP00000469901.1:n.*2067G=
ENST00000595838.5:c.1651G= ENSP00000470501.1:p.Asp551=
ENST00000597188.5:c.3190G= ENSP00000471851.1:p.Asp1064=
NM_001282352.1:c.1651G= NP_001269281.1:p.Asp551=
NM_030957.3:c.3190G= NP_112219.3:p.Asp1064=
XM_006722917.2:c.2233G= XP_006722980.1:p.Asp745=
XM_011528331.1:c.3337G= XP_011526633.1:p.Asp1113=
XM_011528332.1:c.3337G= XP_011526634.1:p.Asp1113=
XM_011528333.1:c.3337G= XP_011526635.1:p.Asp1113=
XM_011528334.1:c.3013G= XP_011526636.1:p.Asp1005=
XM_011528335.1:c.1906G= XP_011526637.1:p.Asp636=
XM_011528336.1:c.1900G= XP_011526638.1:p.Asp634=
XM_006722917.3:c.2233G= XP_006722980.1:p.Asp745=
XM_017027338.2:c.3190G= XP_016882827.1:p.Asp1064=
XM_017027339.1:c.1759G= XP_016882828.1:p.Asp587=
XM_017027340.1:c.1753G= XP_016882829.1:p.Asp585=
NM_030957.4:c.3190G= MANE Select NP_112219.3:p.Asp1064=
NM_001282352.2:c.1651G= NP_001269281.1:p.Asp551=