Canonical Allele Identifier: CA2321496478
Gene: ADAMTS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8584810A= , CM000681.2:g.8584810A= GRCh38
NC_000019.9:g.8649694A= , CM000681.1:g.8649694A= GRCh37
NC_000019.8:g.8555694A= NCBI36
NG_011840.2:g.30893T=

Transcript Alleles

HGVS Amino-acid change
ENST00000597188.6:c.3202+85T= MANE Select ENSP00000471851.1:n.3202+85T=
ENST00000270328.8:c.3202+85T= ENSP00000270328.4:n.3202+85T=
ENST00000593913.5:c.*2079+85T= ENSP00000469901.1:n.*2079+85T=
ENST00000595838.5:c.1663+85T= ENSP00000470501.1:n.1663+85T=
ENST00000597188.5:c.3202+85T= ENSP00000471851.1:n.3202+85T=
NM_001282352.1:c.1663+85T= NP_001269281.1:n.1663+85T=
NM_030957.3:c.3202+85T= NP_112219.3:n.3202+85T=
XM_006722917.2:c.2245+85T= XP_006722980.1:n.2245+85T=
XM_011528331.1:c.3349+85T= XP_011526633.1:n.3349+85T=
XM_011528332.1:c.3349+85T= XP_011526634.1:n.3349+85T=
XM_011528333.1:c.3349+85T= XP_011526635.1:n.3349+85T=
XM_011528334.1:c.3025+85T= XP_011526636.1:n.3025+85T=
XM_011528335.1:c.1918+85T= XP_011526637.1:n.1918+85T=
XM_011528336.1:c.1912+85T= XP_011526638.1:n.1912+85T=
XM_006722917.3:c.2245+85T= XP_006722980.1:n.2245+85T=
XM_017027338.2:c.3202+85T= XP_016882827.1:n.3202+85T=
XM_017027339.1:c.1771+85T= XP_016882828.1:n.1771+85T=
XM_017027340.1:c.1765+85T= XP_016882829.1:n.1765+85T=
NM_030957.4:c.3202+85T= MANE Select NP_112219.3:n.3202+85T=
NM_001282352.2:c.1663+85T= NP_001269281.1:n.1663+85T=