Canonical Allele Identifier: CA2321494721

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580937C= , CM000681.2:g.8580937C=	GRCh38
NC_000019.9:g.8645821C= , CM000681.1:g.8645821C=	GRCh37
NC_000019.8:g.8551821C=	NCBI36
NG_011840.2:g.34766G=
NG_052844.1:g.1511G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3268G= MANE Select	ENSP00000471851.1:p.Ala1090=
ENST00000270328.8:c.3268G=	ENSP00000270328.4:p.Ala1090=
ENST00000593913.5:c.*2145G=	ENSP00000469901.1:n.*2145G=
ENST00000595838.5:c.1729G=	ENSP00000470501.1:p.Ala577=
ENST00000597188.5:c.3268G=	ENSP00000471851.1:p.Ala1090=
NM_001282352.1:c.1729G=	NP_001269281.1:p.Ala577=
NM_030957.3:c.3268G=	NP_112219.3:p.Ala1090=
XM_006722917.2:c.2311G=	XP_006722980.1:p.Ala771=
XM_011528331.1:c.3415G=	XP_011526633.1:p.Ala1139=
XM_011528332.1:c.3415G=	XP_011526634.1:p.Ala1139=
XM_011528333.1:c.3415G=	XP_011526635.1:p.Ala1139=
XM_011528334.1:c.3091G=	XP_011526636.1:p.Ala1031=
XM_011528335.1:c.1984G=	XP_011526637.1:p.Ala662=
XM_011528336.1:c.1978G=	XP_011526638.1:p.Ala660=
XM_006722917.3:c.2311G=	XP_006722980.1:p.Ala771=
XM_017027338.2:c.3268G=	XP_016882827.1:p.Ala1090=
XM_017027339.1:c.1837G=	XP_016882828.1:p.Ala613=
XM_017027340.1:c.1831G=	XP_016882829.1:p.Ala611=
NM_030957.4:c.3268G= MANE Select	NP_112219.3:p.Ala1090=
NM_001282352.2:c.1729G=	NP_001269281.1:p.Ala577=