Canonical Allele Identifier: CA2321494732

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580968G= , CM000681.2:g.8580968G=	GRCh38
NC_000019.9:g.8645852G= , CM000681.1:g.8645852G=	GRCh37
NC_000019.8:g.8551852G=	NCBI36
NG_011840.2:g.34735C=
NG_052844.1:g.1480C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3237C= MANE Select	ENSP00000471851.1:p.Pro1079=
ENST00000270328.8:c.3237C=	ENSP00000270328.4:p.Pro1079=
ENST00000593913.5:c.*2114C=	ENSP00000469901.1:n.*2114C=
ENST00000595838.5:c.1698C=	ENSP00000470501.1:p.Pro566=
ENST00000597188.5:c.3237C=	ENSP00000471851.1:p.Pro1079=
NM_001282352.1:c.1698C=	NP_001269281.1:p.Pro566=
NM_030957.3:c.3237C=	NP_112219.3:p.Pro1079=
XM_006722917.2:c.2280C=	XP_006722980.1:p.Pro760=
XM_011528331.1:c.3384C=	XP_011526633.1:p.Pro1128=
XM_011528332.1:c.3384C=	XP_011526634.1:p.Pro1128=
XM_011528333.1:c.3384C=	XP_011526635.1:p.Pro1128=
XM_011528334.1:c.3060C=	XP_011526636.1:p.Pro1020=
XM_011528335.1:c.1953C=	XP_011526637.1:p.Pro651=
XM_011528336.1:c.1947C=	XP_011526638.1:p.Pro649=
XM_006722917.3:c.2280C=	XP_006722980.1:p.Pro760=
XM_017027338.2:c.3237C=	XP_016882827.1:p.Pro1079=
XM_017027339.1:c.1806C=	XP_016882828.1:p.Pro602=
XM_017027340.1:c.1800C=	XP_016882829.1:p.Pro600=
NM_030957.4:c.3237C= MANE Select	NP_112219.3:p.Pro1079=
NM_001282352.2:c.1698C=	NP_001269281.1:p.Pro566=