Canonical Allele Identifier: CA2321494714

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580920C= , CM000681.2:g.8580920C=	GRCh38
NC_000019.9:g.8645804C= , CM000681.1:g.8645804C=	GRCh37
NC_000019.8:g.8551804C=	NCBI36
NG_011840.2:g.34783G=
NG_052844.1:g.1528G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3285G= MANE Select	ENSP00000471851.1:p.Met1095=
ENST00000270328.8:c.3285G=	ENSP00000270328.4:p.Met1095=
ENST00000593913.5:c.*2162G=	ENSP00000469901.1:n.*2162G=
ENST00000595838.5:c.1746G=	ENSP00000470501.1:p.Met582=
ENST00000597188.5:c.3285G=	ENSP00000471851.1:p.Met1095=
NM_001282352.1:c.1746G=	NP_001269281.1:p.Met582=
NM_030957.3:c.3285G=	NP_112219.3:p.Met1095=
XM_006722917.2:c.2328G=	XP_006722980.1:p.Met776=
XM_011528331.1:c.3432G=	XP_011526633.1:p.Met1144=
XM_011528332.1:c.3432G=	XP_011526634.1:p.Met1144=
XM_011528333.1:c.3432G=	XP_011526635.1:p.Met1144=
XM_011528334.1:c.3108G=	XP_011526636.1:p.Met1036=
XM_011528335.1:c.2001G=	XP_011526637.1:p.Met667=
XM_011528336.1:c.1995G=	XP_011526638.1:p.Met665=
XM_006722917.3:c.2328G=	XP_006722980.1:p.Met776=
XM_017027338.2:c.3285G=	XP_016882827.1:p.Met1095=
XM_017027339.1:c.1854G=	XP_016882828.1:p.Met618=
XM_017027340.1:c.1848G=	XP_016882829.1:p.Met616=
NM_030957.4:c.3285G= MANE Select	NP_112219.3:p.Met1095=
NM_001282352.2:c.1746G=	NP_001269281.1:p.Met582=