Canonical Allele Identifier: CA2321504179

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8601017C= , CM000681.2:g.8601017C=	GRCh38
NC_000019.9:g.8665901C= , CM000681.1:g.8665901C=	GRCh37
NC_000019.8:g.8571901C=	NCBI36
NG_011840.2:g.14686G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.721G= MANE Select	ENSP00000471851.1:p.Val241=
ENST00000270328.8:c.721G=	ENSP00000270328.4:p.Val241=
ENST00000593913.5:c.721G=	ENSP00000469901.1:p.Val241=
ENST00000596466.2:n.670G=
ENST00000596709.5:n.805G=
ENST00000596851.5:c.721G=	ENSP00000469559.1:p.Val241=
ENST00000597188.5:c.721G=	ENSP00000471851.1:p.Val241=
NM_030957.3:c.721G=	NP_112219.3:p.Val241=
XM_006722917.2:c.-389G=	XP_006722980.1:n.-389G=
XM_011528331.1:c.721G=	XP_011526633.1:p.Val241=
XM_011528332.1:c.721G=	XP_011526634.1:p.Val241=
XM_011528333.1:c.721G=	XP_011526635.1:p.Val241=
XM_011528334.1:c.721G=	XP_011526636.1:p.Val241=
XR_430156.2:n.997G=
XR_936208.1:n.997G=
XR_936209.1:n.997G=
XM_006722917.3:c.-389G=	XP_006722980.1:n.-389G=
XM_017027338.2:c.721G=	XP_016882827.1:p.Val241=
XR_001753770.1:n.1557G=
NM_030957.4:c.721G= MANE Select	NP_112219.3:p.Val241=