Canonical Allele Identifier: CA2841831012

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8597185G>T , CM000681.2:g.8597185G>T	GRCh38
NC_000019.9:g.8662069G>T , CM000681.1:g.8662069G>T	GRCh37
NC_000019.8:g.8568069G>T	NCBI36
NG_011840.2:g.18518C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.894+49C>A MANE Select	ENSP00000471851.1:n.894+49C>A
ENST00000270328.8:c.894+49C>A	ENSP00000270328.4:n.894+49C>A
ENST00000593913.5:c.*29+49C>A	ENSP00000469901.1:n.*29+49C>A
ENST00000596851.5:c.*29+49C>A	ENSP00000469559.1:n.*29+49C>A
ENST00000597188.5:c.894+49C>A	ENSP00000471851.1:n.894+49C>A
ENST00000601163.1:n.89+49C>A
NM_030957.3:c.894+49C>A	NP_112219.3:n.894+49C>A
XM_006722917.2:c.-211+49C>A	XP_006722980.1:n.-211+49C>A
XM_011528331.1:c.894+49C>A	XP_011526633.1:n.894+49C>A
XM_011528332.1:c.894+49C>A	XP_011526634.1:n.894+49C>A
XM_011528333.1:c.894+49C>A	XP_011526635.1:n.894+49C>A
XM_011528334.1:c.894+49C>A	XP_011526636.1:n.894+49C>A
XR_430156.2:n.1170+49C>A
XR_936208.1:n.1170+49C>A
XR_936209.1:n.1170+49C>A
XM_006722917.3:c.-211+49C>A	XP_006722980.1:n.-211+49C>A
XM_017027338.2:c.894+49C>A	XP_016882827.1:n.894+49C>A
XR_001753770.1:n.1730+49C>A
NM_030957.4:c.894+49C>A MANE Select	NP_112219.3:n.894+49C>A