Canonical Allele Identifier: CA505262971

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645807C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3282G>A MANE Select	ENSP00000471851.1:p.Gln1094=
ENST00000270328.8:c.3282G>A	ENSP00000270328.4:p.Gln1094=
ENST00000593913.5:c.*2159G>A	ENSP00000469901.1:n.*2159G>A
ENST00000595838.5:c.1743G>A	ENSP00000470501.1:p.Gln581=
ENST00000597188.5:c.3282G>A	ENSP00000471851.1:p.Gln1094=
NM_001282352.1:c.1743G>A	NP_001269281.1:p.Gln581=
NM_030957.3:c.3282G>A	NP_112219.3:p.Gln1094=
XM_006722917.2:c.2325G>A	XP_006722980.1:p.Gln775=
XM_011528331.1:c.3429G>A	XP_011526633.1:p.Gln1143=
XM_011528332.1:c.3429G>A	XP_011526634.1:p.Gln1143=
XM_011528333.1:c.3429G>A	XP_011526635.1:p.Gln1143=
XM_011528334.1:c.3105G>A	XP_011526636.1:p.Gln1035=
XM_011528335.1:c.1998G>A	XP_011526637.1:p.Gln666=
XM_011528336.1:c.1992G>A	XP_011526638.1:p.Gln664=
XM_006722917.3:c.2325G>A	XP_006722980.1:p.Gln775=
XM_017027338.2:c.3282G>A	XP_016882827.1:p.Gln1094=
XM_017027339.1:c.1851G>A	XP_016882828.1:p.Gln617=
XM_017027340.1:c.1845G>A	XP_016882829.1:p.Gln615=
NM_030957.4:c.3282G>A MANE Select	NP_112219.3:p.Gln1094=
NM_001282352.2:c.1743G>A	NP_001269281.1:p.Gln581=