Canonical Allele Identifier: CA9160598

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8596314C>T , CM000681.2:g.8596314C>T	GRCh38
NC_000019.9:g.8661198C>T , CM000681.1:g.8661198C>T	GRCh37
NC_000019.8:g.8567198C>T	NCBI36
NG_011840.2:g.19389G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.1183G>A MANE Select	ENSP00000471851.1:p.Gly395Arg
ENST00000270328.8:c.1183G>A	ENSP00000270328.4:p.Gly395Arg
ENST00000593913.5:c.*79-95G>A	ENSP00000469901.1:n.*79-95G>A
ENST00000596851.5:c.*318G>A	ENSP00000469559.1:n.*318G>A
ENST00000597188.5:c.1183G>A	ENSP00000471851.1:p.Gly395Arg
ENST00000601163.1:n.378G>A
ENST00000601872.1:n.44G>A
NM_030957.3:c.1183G>A	NP_112219.3:p.Gly395Arg
XM_006722917.2:c.79G>A	XP_006722980.1:p.Gly27Arg
XM_011528331.1:c.1183G>A	XP_011526633.1:p.Gly395Arg
XM_011528332.1:c.1183G>A	XP_011526634.1:p.Gly395Arg
XM_011528333.1:c.1183G>A	XP_011526635.1:p.Gly395Arg
XM_011528334.1:c.1183G>A	XP_011526636.1:p.Gly395Arg
XR_430156.2:n.1459G>A
XR_936208.1:n.1459G>A
XR_936209.1:n.1459G>A
XM_006722917.3:c.79G>A	XP_006722980.1:p.Gly27Arg
XM_017027338.2:c.1183G>A	XP_016882827.1:p.Gly395Arg
XR_001753770.1:n.2019G>A
NM_030957.4:c.1183G>A MANE Select	NP_112219.3:p.Gly395Arg