Canonical Allele Identifier: CA2321494723

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580941G= , CM000681.2:g.8580941G=	GRCh38
NC_000019.9:g.8645825G= , CM000681.1:g.8645825G=	GRCh37
NC_000019.8:g.8551825G=	NCBI36
NG_011840.2:g.34762C=
NG_052844.1:g.1507C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3264C= MANE Select	ENSP00000471851.1:p.Ser1088=
ENST00000270328.8:c.3264C=	ENSP00000270328.4:p.Ser1088=
ENST00000593913.5:c.*2141C=	ENSP00000469901.1:n.*2141C=
ENST00000595838.5:c.1725C=	ENSP00000470501.1:p.Ser575=
ENST00000597188.5:c.3264C=	ENSP00000471851.1:p.Ser1088=
NM_001282352.1:c.1725C=	NP_001269281.1:p.Ser575=
NM_030957.3:c.3264C=	NP_112219.3:p.Ser1088=
XM_006722917.2:c.2307C=	XP_006722980.1:p.Ser769=
XM_011528331.1:c.3411C=	XP_011526633.1:p.Ser1137=
XM_011528332.1:c.3411C=	XP_011526634.1:p.Ser1137=
XM_011528333.1:c.3411C=	XP_011526635.1:p.Ser1137=
XM_011528334.1:c.3087C=	XP_011526636.1:p.Ser1029=
XM_011528335.1:c.1980C=	XP_011526637.1:p.Ser660=
XM_011528336.1:c.1974C=	XP_011526638.1:p.Ser658=
XM_006722917.3:c.2307C=	XP_006722980.1:p.Ser769=
XM_017027338.2:c.3264C=	XP_016882827.1:p.Ser1088=
XM_017027339.1:c.1833C=	XP_016882828.1:p.Ser611=
XM_017027340.1:c.1827C=	XP_016882829.1:p.Ser609=
NM_030957.4:c.3264C= MANE Select	NP_112219.3:p.Ser1088=
NM_001282352.2:c.1725C=	NP_001269281.1:p.Ser575=