Canonical Allele Identifier: CA403747827
Gene: ADAMTS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8580921A>C , CM000681.2:g.8580921A>C GRCh38
NC_000019.9:g.8645805A>C , CM000681.1:g.8645805A>C GRCh37
NC_000019.8:g.8551805A>C NCBI36
NG_011840.2:g.34782T>G
NG_052844.1:g.1527T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.3284T>G MANE Select ENSP00000471851.1:p.Met1095Arg
ENST00000270328.8:c.3284T>G ENSP00000270328.4:p.Met1095Arg
ENST00000593913.5:c.*2161T>G ENSP00000469901.1:n.*2161T>G
ENST00000595838.5:c.1745T>G ENSP00000470501.1:p.Met582Arg
ENST00000597188.5:c.3284T>G ENSP00000471851.1:p.Met1095Arg
NM_001282352.1:c.1745T>G NP_001269281.1:p.Met582Arg
NM_030957.3:c.3284T>G NP_112219.3:p.Met1095Arg
XM_006722917.2:c.2327T>G XP_006722980.1:p.Met776Arg
XM_011528331.1:c.3431T>G XP_011526633.1:p.Met1144Arg
XM_011528332.1:c.3431T>G XP_011526634.1:p.Met1144Arg
XM_011528333.1:c.3431T>G XP_011526635.1:p.Met1144Arg
XM_011528334.1:c.3107T>G XP_011526636.1:p.Met1036Arg
XM_011528335.1:c.2000T>G XP_011526637.1:p.Met667Arg
XM_011528336.1:c.1994T>G XP_011526638.1:p.Met665Arg
XM_006722917.3:c.2327T>G XP_006722980.1:p.Met776Arg
XM_017027338.2:c.3284T>G XP_016882827.1:p.Met1095Arg
XM_017027339.1:c.1853T>G XP_016882828.1:p.Met618Arg
XM_017027340.1:c.1847T>G XP_016882829.1:p.Met616Arg
NM_030957.4:c.3284T>G MANE Select NP_112219.3:p.Met1095Arg
NM_001282352.2:c.1745T>G NP_001269281.1:p.Met582Arg