Canonical Allele Identifier: CA2588115863
Gene: ADAMTS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8580659_8580661dup , CM000681.2:g.8580659_8580661dup GRCh38
NC_000019.9:g.8645543_8645545dup , CM000681.1:g.8645543_8645545dup GRCh37
NC_000019.8:g.8551543_8551545dup NCBI36
NG_011840.2:g.35046_35048dup
NG_052844.1:g.1791_1793dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.*236_*238dup MANE Select ENSP00000471851.1:n.*236_*238dup
ENST00000270328.8:c.*236_*238dup ENSP00000270328.4:n.*236_*238dup
ENST00000595838.5:c.*236_*238dup ENSP00000470501.1:n.*236_*238dup
NM_001282352.1:c.*236_*238dup NP_001269281.1:n.*236_*238dup
NM_030957.3:c.*236_*238dup NP_112219.3:n.*236_*238dup
XM_006722917.2:c.*236_*238dup XP_006722980.1:n.*236_*238dup
XM_011528331.1:c.*236_*238dup XP_011526633.1:n.*236_*238dup
XM_011528332.1:c.*236_*238dup XP_011526634.1:n.*236_*238dup
XM_011528333.1:c.*236_*238dup XP_011526635.1:n.*236_*238dup
XM_011528334.1:c.*236_*238dup XP_011526636.1:n.*236_*238dup
XM_011528335.1:c.*236_*238dup XP_011526637.1:n.*236_*238dup
XM_011528336.1:c.*236_*238dup XP_011526638.1:n.*236_*238dup
XM_006722917.3:c.*236_*238dup XP_006722980.1:n.*236_*238dup
XM_017027339.1:c.*236_*238dup XP_016882828.1:n.*236_*238dup
XM_017027340.1:c.*236_*238dup XP_016882829.1:n.*236_*238dup
NM_030957.4:c.*236_*238dup MANE Select NP_112219.3:n.*236_*238dup
NM_001282352.2:c.*236_*238dup NP_001269281.1:n.*236_*238dup