Canonical Allele Identifier: CA2321494718

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580927C= , CM000681.2:g.8580927C=	GRCh38
NC_000019.9:g.8645811C= , CM000681.1:g.8645811C=	GRCh37
NC_000019.8:g.8551811C=	NCBI36
NG_011840.2:g.34776G=
NG_052844.1:g.1521G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3278G= MANE Select	ENSP00000471851.1:p.Arg1093=
ENST00000270328.8:c.3278G=	ENSP00000270328.4:p.Arg1093=
ENST00000593913.5:c.*2155G=	ENSP00000469901.1:n.*2155G=
ENST00000595838.5:c.1739G=	ENSP00000470501.1:p.Arg580=
ENST00000597188.5:c.3278G=	ENSP00000471851.1:p.Arg1093=
NM_001282352.1:c.1739G=	NP_001269281.1:p.Arg580=
NM_030957.3:c.3278G=	NP_112219.3:p.Arg1093=
XM_006722917.2:c.2321G=	XP_006722980.1:p.Arg774=
XM_011528331.1:c.3425G=	XP_011526633.1:p.Arg1142=
XM_011528332.1:c.3425G=	XP_011526634.1:p.Arg1142=
XM_011528333.1:c.3425G=	XP_011526635.1:p.Arg1142=
XM_011528334.1:c.3101G=	XP_011526636.1:p.Arg1034=
XM_011528335.1:c.1994G=	XP_011526637.1:p.Arg665=
XM_011528336.1:c.1988G=	XP_011526638.1:p.Arg663=
XM_006722917.3:c.2321G=	XP_006722980.1:p.Arg774=
XM_017027338.2:c.3278G=	XP_016882827.1:p.Arg1093=
XM_017027339.1:c.1847G=	XP_016882828.1:p.Arg616=
XM_017027340.1:c.1841G=	XP_016882829.1:p.Arg614=
NM_030957.4:c.3278G= MANE Select	NP_112219.3:p.Arg1093=
NM_001282352.2:c.1739G=	NP_001269281.1:p.Arg580=