Canonical Allele Identifier: CA505262987

Gene: ADAMTS10

Linked Data

• gnomAD v4: 19-8580926-G-T
• MyVariant Identifiers: chr19:g.8645810G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580926G>T , CM000681.2:g.8580926G>T	GRCh38
NC_000019.9:g.8645810G>T , CM000681.1:g.8645810G>T	GRCh37
NC_000019.8:g.8551810G>T	NCBI36
NG_011840.2:g.34777C>A
NG_052844.1:g.1522C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3279C>A MANE Select	ENSP00000471851.1:p.Arg1093=
ENST00000270328.8:c.3279C>A	ENSP00000270328.4:p.Arg1093=
ENST00000593913.5:c.*2156C>A	ENSP00000469901.1:n.*2156C>A
ENST00000595838.5:c.1740C>A	ENSP00000470501.1:p.Arg580=
ENST00000597188.5:c.3279C>A	ENSP00000471851.1:p.Arg1093=
NM_001282352.1:c.1740C>A	NP_001269281.1:p.Arg580=
NM_030957.3:c.3279C>A	NP_112219.3:p.Arg1093=
XM_006722917.2:c.2322C>A	XP_006722980.1:p.Arg774=
XM_011528331.1:c.3426C>A	XP_011526633.1:p.Arg1142=
XM_011528332.1:c.3426C>A	XP_011526634.1:p.Arg1142=
XM_011528333.1:c.3426C>A	XP_011526635.1:p.Arg1142=
XM_011528334.1:c.3102C>A	XP_011526636.1:p.Arg1034=
XM_011528335.1:c.1995C>A	XP_011526637.1:p.Arg665=
XM_011528336.1:c.1989C>A	XP_011526638.1:p.Arg663=
XM_006722917.3:c.2322C>A	XP_006722980.1:p.Arg774=
XM_017027338.2:c.3279C>A	XP_016882827.1:p.Arg1093=
XM_017027339.1:c.1848C>A	XP_016882828.1:p.Arg616=
XM_017027340.1:c.1842C>A	XP_016882829.1:p.Arg614=
NM_030957.4:c.3279C>A MANE Select	NP_112219.3:p.Arg1093=
NM_001282352.2:c.1740C>A	NP_001269281.1:p.Arg580=