Canonical Allele Identifier: CA2321507056

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8607115G= , CM000681.2:g.8607115G=	GRCh38
NC_000019.9:g.8672000G= , CM000681.1:g.8672000G=	GRCh37
NC_000019.8:g.8578000G=	NCBI36
NG_011840.2:g.8588C=

Transcript Alleles

HGVS	Amino-acid Change
NM_030957.4:c.-100+1019C= MANE Select	NP_112219.3:n.-100+1019C=
ENST00000597188.6:c.-100+1019C= MANE Select	ENSP00000471851.1:n.-100+1019C=
NM_030957.3:c.-100+1019C=	NP_112219.3:n.-100+1019C=
ENST00000270328.8:c.-100+1019C=	ENSP00000270328.4:n.-100+1019C=
ENST00000593534.1:n.207+1019C=
ENST00000596466.2:n.38-1757C=
ENST00000596709.5:n.172+1019C=
ENST00000596851.5:c.-99-1306C=	ENSP00000469559.1:n.-99-1306C=
ENST00000597188.5:c.-100+1019C=	ENSP00000471851.1:n.-100+1019C=
XM_006722917.2:c.-1208-1306C=	XP_006722980.1:n.-1208-1306C=
XM_006722917.3:c.-1208-1306C=	XP_006722980.1:n.-1208-1306C=
XM_011528331.1:c.-100+1019C=	XP_011526633.1:n.-100+1019C=
XM_011528332.1:c.-100+1019C=	XP_011526634.1:n.-100+1019C=
XM_011528333.1:c.-99-1306C=	XP_011526635.1:n.-99-1306C=
XM_011528334.1:c.-100+1019C=	XP_011526636.1:n.-100+1019C=
XM_017027338.2:c.-99-1306C=	XP_016882827.1:n.-99-1306C=
XR_001753770.1:n.737+1019C=
XR_430156.2:n.177+1019C=
XR_936208.1:n.177+1019C=
XR_936209.1:n.177+1019C=