Canonical Allele Identifier: CA403747915

Gene: ADAMTS10

Linked Data

• COSMIC: COSM1711745
• MyVariant Identifiers: chr19:g.8645839A>T (hg19) ; chr19:g.8580955A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580955A>T , CM000681.2:g.8580955A>T	GRCh38
NC_000019.9:g.8645839A>T , CM000681.1:g.8645839A>T	GRCh37
NC_000019.8:g.8551839A>T	NCBI36
NG_011840.2:g.34748T>A
NG_052844.1:g.1493T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3250T>A MANE Select	ENSP00000471851.1:p.Phe1084Ile
ENST00000270328.8:c.3250T>A	ENSP00000270328.4:p.Phe1084Ile
ENST00000593913.5:c.*2127T>A	ENSP00000469901.1:n.*2127T>A
ENST00000595838.5:c.1711T>A	ENSP00000470501.1:p.Phe571Ile
ENST00000597188.5:c.3250T>A	ENSP00000471851.1:p.Phe1084Ile
NM_001282352.1:c.1711T>A	NP_001269281.1:p.Phe571Ile
NM_030957.3:c.3250T>A	NP_112219.3:p.Phe1084Ile
XM_006722917.2:c.2293T>A	XP_006722980.1:p.Phe765Ile
XM_011528331.1:c.3397T>A	XP_011526633.1:p.Phe1133Ile
XM_011528332.1:c.3397T>A	XP_011526634.1:p.Phe1133Ile
XM_011528333.1:c.3397T>A	XP_011526635.1:p.Phe1133Ile
XM_011528334.1:c.3073T>A	XP_011526636.1:p.Phe1025Ile
XM_011528335.1:c.1966T>A	XP_011526637.1:p.Phe656Ile
XM_011528336.1:c.1960T>A	XP_011526638.1:p.Phe654Ile
XM_006722917.3:c.2293T>A	XP_006722980.1:p.Phe765Ile
XM_017027338.2:c.3250T>A	XP_016882827.1:p.Phe1084Ile
XM_017027339.1:c.1819T>A	XP_016882828.1:p.Phe607Ile
XM_017027340.1:c.1813T>A	XP_016882829.1:p.Phe605Ile
NM_030957.4:c.3250T>A MANE Select	NP_112219.3:p.Phe1084Ile
NM_001282352.2:c.1711T>A	NP_001269281.1:p.Phe571Ile