Canonical Allele Identifier: CA2588116802

Gene: ADAMTS10

Linked Data

• gnomAD v4: 19-8584829-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8584829C>A , CM000681.2:g.8584829C>A	GRCh38
NC_000019.9:g.8649713C>A , CM000681.1:g.8649713C>A	GRCh37
NC_000019.8:g.8555713C>A	NCBI36
NG_011840.2:g.30874G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.3202+66G>T MANE Select	ENSP00000471851.1:n.3202+66G>T
ENST00000270328.8:c.3202+66G>T	ENSP00000270328.4:n.3202+66G>T
ENST00000593913.5:c.*2079+66G>T	ENSP00000469901.1:n.*2079+66G>T
ENST00000595838.5:c.1663+66G>T	ENSP00000470501.1:n.1663+66G>T
ENST00000597188.5:c.3202+66G>T	ENSP00000471851.1:n.3202+66G>T
NM_001282352.1:c.1663+66G>T	NP_001269281.1:n.1663+66G>T
NM_030957.3:c.3202+66G>T	NP_112219.3:n.3202+66G>T
XM_006722917.2:c.2245+66G>T	XP_006722980.1:n.2245+66G>T
XM_011528331.1:c.3349+66G>T	XP_011526633.1:n.3349+66G>T
XM_011528332.1:c.3349+66G>T	XP_011526634.1:n.3349+66G>T
XM_011528333.1:c.3349+66G>T	XP_011526635.1:n.3349+66G>T
XM_011528334.1:c.3025+66G>T	XP_011526636.1:n.3025+66G>T
XM_011528335.1:c.1918+66G>T	XP_011526637.1:n.1918+66G>T
XM_011528336.1:c.1912+66G>T	XP_011526638.1:n.1912+66G>T
XM_006722917.3:c.2245+66G>T	XP_006722980.1:n.2245+66G>T
XM_017027338.2:c.3202+66G>T	XP_016882827.1:n.3202+66G>T
XM_017027339.1:c.1771+66G>T	XP_016882828.1:n.1771+66G>T
XM_017027340.1:c.1765+66G>T	XP_016882829.1:n.1765+66G>T
NM_030957.4:c.3202+66G>T MANE Select	NP_112219.3:n.3202+66G>T
NM_001282352.2:c.1663+66G>T	NP_001269281.1:n.1663+66G>T