Canonical Allele Identifier: CA403747834

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645807C>A (hg19) ; chr19:g.8580923C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580923C>A , CM000681.2:g.8580923C>A	GRCh38
NC_000019.9:g.8645807C>A , CM000681.1:g.8645807C>A	GRCh37
NC_000019.8:g.8551807C>A	NCBI36
NG_011840.2:g.34780G>T
NG_052844.1:g.1525G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3282G>T MANE Select	ENSP00000471851.1:p.Gln1094His
ENST00000270328.8:c.3282G>T	ENSP00000270328.4:p.Gln1094His
ENST00000593913.5:c.*2159G>T	ENSP00000469901.1:n.*2159G>T
ENST00000595838.5:c.1743G>T	ENSP00000470501.1:p.Gln581His
ENST00000597188.5:c.3282G>T	ENSP00000471851.1:p.Gln1094His
NM_001282352.1:c.1743G>T	NP_001269281.1:p.Gln581His
NM_030957.3:c.3282G>T	NP_112219.3:p.Gln1094His
XM_006722917.2:c.2325G>T	XP_006722980.1:p.Gln775His
XM_011528331.1:c.3429G>T	XP_011526633.1:p.Gln1143His
XM_011528332.1:c.3429G>T	XP_011526634.1:p.Gln1143His
XM_011528333.1:c.3429G>T	XP_011526635.1:p.Gln1143His
XM_011528334.1:c.3105G>T	XP_011526636.1:p.Gln1035His
XM_011528335.1:c.1998G>T	XP_011526637.1:p.Gln666His
XM_011528336.1:c.1992G>T	XP_011526638.1:p.Gln664His
XM_006722917.3:c.2325G>T	XP_006722980.1:p.Gln775His
XM_017027338.2:c.3282G>T	XP_016882827.1:p.Gln1094His
XM_017027339.1:c.1851G>T	XP_016882828.1:p.Gln617His
XM_017027340.1:c.1845G>T	XP_016882829.1:p.Gln615His
NM_030957.4:c.3282G>T MANE Select	NP_112219.3:p.Gln1094His
NM_001282352.2:c.1743G>T	NP_001269281.1:p.Gln581His