Canonical Allele Identifier: CA2321503951

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8600665_8600667delinsATT , CM000681.2:g.8600665_8600667delinsATT	GRCh38
NC_000019.9:g.8665549_8665551delinsATT , CM000681.1:g.8665549_8665551delinsATT	GRCh37
NC_000019.8:g.8571549_8571551delinsATT	NCBI36
NG_011840.2:g.15036_15038delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.810+261_810+263delinsAAT MANE Select	ENSP00000471851.1:n.810+261_810+263delinsAAT
ENST00000270328.8:c.810+261_810+263delinsAAT	ENSP00000270328.4:n.810+261_810+263delinsAAT
ENST00000593913.5:c.810+261_810+263delinsAAT	ENSP00000469901.1:n.810+261_810+263delinsAAT
ENST00000596466.2:n.759+261_759+263delinsAAT
ENST00000596709.5:n.894+261_894+263delinsAAT
ENST00000596851.5:c.810+261_810+263delinsAAT	ENSP00000469559.1:n.810+261_810+263delinsAAT
ENST00000597188.5:c.810+261_810+263delinsAAT	ENSP00000471851.1:n.810+261_810+263delinsAAT
NM_030957.3:c.810+261_810+263delinsAAT	NP_112219.3:n.810+261_810+263delinsAAT
XM_006722917.2:c.-300+261_-300+263delinsAAT	XP_006722980.1:n.-300+261_-300+263delinsAAT
XM_011528331.1:c.810+261_810+263delinsAAT	XP_011526633.1:n.810+261_810+263delinsAAT
XM_011528332.1:c.810+261_810+263delinsAAT	XP_011526634.1:n.810+261_810+263delinsAAT
XM_011528333.1:c.810+261_810+263delinsAAT	XP_011526635.1:n.810+261_810+263delinsAAT
XM_011528334.1:c.810+261_810+263delinsAAT	XP_011526636.1:n.810+261_810+263delinsAAT
XR_430156.2:n.1086+261_1086+263delinsAAT
XR_936208.1:n.1086+261_1086+263delinsAAT
XR_936209.1:n.1086+261_1086+263delinsAAT
XM_006722917.3:c.-300+261_-300+263delinsAAT	XP_006722980.1:n.-300+261_-300+263delinsAAT
XM_017027338.2:c.810+261_810+263delinsAAT	XP_016882827.1:n.810+261_810+263delinsAAT
XR_001753770.1:n.1646+261_1646+263delinsAAT
NM_030957.4:c.810+261_810+263delinsAAT MANE Select	NP_112219.3:n.810+261_810+263delinsAAT