Canonical Allele Identifier: CA403747933

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645847A>T (hg19) ; chr19:g.8580963A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580963A>T , CM000681.2:g.8580963A>T	GRCh38
NC_000019.9:g.8645847A>T , CM000681.1:g.8645847A>T	GRCh37
NC_000019.8:g.8551847A>T	NCBI36
NG_011840.2:g.34740T>A
NG_052844.1:g.1485T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3242T>A MANE Select	ENSP00000471851.1:p.Val1081Glu
ENST00000270328.8:c.3242T>A	ENSP00000270328.4:p.Val1081Glu
ENST00000593913.5:c.*2119T>A	ENSP00000469901.1:n.*2119T>A
ENST00000595838.5:c.1703T>A	ENSP00000470501.1:p.Val568Glu
ENST00000597188.5:c.3242T>A	ENSP00000471851.1:p.Val1081Glu
NM_001282352.1:c.1703T>A	NP_001269281.1:p.Val568Glu
NM_030957.3:c.3242T>A	NP_112219.3:p.Val1081Glu
XM_006722917.2:c.2285T>A	XP_006722980.1:p.Val762Glu
XM_011528331.1:c.3389T>A	XP_011526633.1:p.Val1130Glu
XM_011528332.1:c.3389T>A	XP_011526634.1:p.Val1130Glu
XM_011528333.1:c.3389T>A	XP_011526635.1:p.Val1130Glu
XM_011528334.1:c.3065T>A	XP_011526636.1:p.Val1022Glu
XM_011528335.1:c.1958T>A	XP_011526637.1:p.Val653Glu
XM_011528336.1:c.1952T>A	XP_011526638.1:p.Val651Glu
XM_006722917.3:c.2285T>A	XP_006722980.1:p.Val762Glu
XM_017027338.2:c.3242T>A	XP_016882827.1:p.Val1081Glu
XM_017027339.1:c.1811T>A	XP_016882828.1:p.Val604Glu
XM_017027340.1:c.1805T>A	XP_016882829.1:p.Val602Glu
NM_030957.4:c.3242T>A MANE Select	NP_112219.3:p.Val1081Glu
NM_001282352.2:c.1703T>A	NP_001269281.1:p.Val568Glu