Canonical Allele Identifier: CA2321494646
Gene: ADAMTS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8580832_8580864delinsGCCCGCTGCAGGGCTGGCGGCGGAGACCCCGCC , CM000681.2:g.8580832_8580864delinsGCCCGCTGCAGGGCTGGCGGCGGAGACCCCGCC GRCh38
NC_000019.9:g.8645716_8645748delinsGCCCGCTGCAGGGCTGGCGGCGGAGACCCCGCC , CM000681.1:g.8645716_8645748delinsGCCCGCTGCAGGGCTGGCGGCGGAGACCCCGCC GRCh37
NC_000019.8:g.8551716_8551748delinsGCCCGCTGCAGGGCTGGCGGCGGAGACCCCGCC NCBI36
NG_011840.2:g.34839_34871delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC
NG_052844.1:g.1584_1616delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC MANE Select ENSP00000471851.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAG...
ENST00000270328.8:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC ENSP00000270328.4:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAG...
ENST00000593913.5:c.*2218_*2250delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC ENSP00000469901.1:n.*2218_*2250delinsGGCGGGGTCTCCGCCGCCAGCCCT...
ENST00000595838.5:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC ENSP00000470501.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAG...
ENST00000597188.5:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC ENSP00000471851.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAG...
NM_001282352.1:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC NP_001269281.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
NM_030957.3:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC NP_112219.3:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC
XM_006722917.2:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_006722980.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
XM_011528331.1:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_011526633.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
XM_011528332.1:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_011526634.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
XM_011528333.1:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_011526635.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
XM_011528334.1:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_011526636.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
XM_011528335.1:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_011526637.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
XM_011528336.1:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_011526638.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
XM_006722917.3:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_006722980.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
XM_017027338.2:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_016882827.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
XM_017027339.1:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_016882828.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
XM_017027340.1:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC XP_016882829.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...
NM_030957.4:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC MANE Select NP_112219.3:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC
NM_001282352.2:c.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGGGC NP_001269281.1:n.*29_*61delinsGGCGGGGTCTCCGCCGCCAGCCCTGCAGCGG...