Canonical Allele Identifier: CA16567667

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8592282C>A , CM000681.2:g.8592282C>A	GRCh38
NC_000019.9:g.8657166C>A , CM000681.1:g.8657166C>A	GRCh37
NC_000019.8:g.8563166C>A	NCBI36
NG_011840.2:g.23421G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_030957.4:c.1588-179G>T MANE Select	NP_112219.3:n.1588-179G>T
ENST00000597188.6:c.1588-179G>T MANE Select	ENSP00000471851.1:n.1588-179G>T
NM_030957.3:c.1588-179G>T	NP_112219.3:n.1588-179G>T
ENST00000270328.8:c.1588-179G>T	ENSP00000270328.4:n.1588-179G>T
ENST00000593913.5:c.*465-179G>T	ENSP00000469901.1:n.*465-179G>T
ENST00000596851.5:c.*723-179G>T	ENSP00000469559.1:n.*723-179G>T
ENST00000597188.5:c.1588-179G>T	ENSP00000471851.1:n.1588-179G>T
ENST00000601163.1:n.870-179G>T
ENST00000603221.5:n.755-179G>T
XM_006722917.2:c.484-179G>T	XP_006722980.1:n.484-179G>T
XM_006722917.3:c.484-179G>T	XP_006722980.1:n.484-179G>T
XM_011528331.1:c.1588-179G>T	XP_011526633.1:n.1588-179G>T
XM_011528332.1:c.1588-179G>T	XP_011526634.1:n.1588-179G>T
XM_011528333.1:c.1588-179G>T	XP_011526635.1:n.1588-179G>T
XM_011528334.1:c.1588-179G>T	XP_011526636.1:n.1588-179G>T
XM_011528335.1:c.157-179G>T	XP_011526637.1:n.157-179G>T
XM_011528336.1:c.151-179G>T	XP_011526638.1:n.151-179G>T
XM_017027338.2:c.1588-179G>T	XP_016882827.1:n.1588-179G>T
XM_017027339.1:c.157-179G>T	XP_016882828.1:n.157-179G>T
XM_017027340.1:c.151-179G>T	XP_016882829.1:n.151-179G>T
XR_001753770.1:n.2424-179G>T
XR_430156.2:n.1847-179G>T
XR_936208.1:n.1864-179G>T
XR_936209.1:n.1847-179G>T