Canonical Allele Identifier: CA2321494573

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580737_8580738delinsCA , CM000681.2:g.8580737_8580738delinsCA	GRCh38
NC_000019.9:g.8645621_8645622delinsCA , CM000681.1:g.8645621_8645622delinsCA	GRCh37
NC_000019.8:g.8551621_8551622delinsCA	NCBI36
NG_011840.2:g.34965_34966delinsTG
NG_052844.1:g.1710_1711delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.*155_*156delinsTG MANE Select	ENSP00000471851.1:n.*155_*156delinsTG
ENST00000270328.8:c.*155_*156delinsTG	ENSP00000270328.4:n.*155_*156delinsTG
ENST00000593913.5:c.*2344_*2345delinsTG	ENSP00000469901.1:n.*2344_*2345delinsTG
ENST00000595838.5:c.*155_*156delinsTG	ENSP00000470501.1:n.*155_*156delinsTG
ENST00000597188.5:c.*155_*156delinsTG	ENSP00000471851.1:n.*155_*156delinsTG
NM_001282352.1:c.*155_*156delinsTG	NP_001269281.1:n.*155_*156delinsTG
NM_030957.3:c.*155_*156delinsTG	NP_112219.3:n.*155_*156delinsTG
XM_006722917.2:c.*155_*156delinsTG	XP_006722980.1:n.*155_*156delinsTG
XM_011528331.1:c.*155_*156delinsTG	XP_011526633.1:n.*155_*156delinsTG
XM_011528332.1:c.*155_*156delinsTG	XP_011526634.1:n.*155_*156delinsTG
XM_011528333.1:c.*155_*156delinsTG	XP_011526635.1:n.*155_*156delinsTG
XM_011528334.1:c.*155_*156delinsTG	XP_011526636.1:n.*155_*156delinsTG
XM_011528335.1:c.*155_*156delinsTG	XP_011526637.1:n.*155_*156delinsTG
XM_011528336.1:c.*155_*156delinsTG	XP_011526638.1:n.*155_*156delinsTG
XM_006722917.3:c.*155_*156delinsTG	XP_006722980.1:n.*155_*156delinsTG
XM_017027338.2:c.*155_*156delinsTG	XP_016882827.1:n.*155_*156delinsTG
XM_017027339.1:c.*155_*156delinsTG	XP_016882828.1:n.*155_*156delinsTG
XM_017027340.1:c.*155_*156delinsTG	XP_016882829.1:n.*155_*156delinsTG
NM_030957.4:c.*155_*156delinsTG MANE Select	NP_112219.3:n.*155_*156delinsTG
NM_001282352.2:c.*155_*156delinsTG	NP_001269281.1:n.*155_*156delinsTG