Canonical Allele Identifier: CA403747766

Gene: ADAMTS10

Linked Data

• gnomAD v4: 19-8580896-G-T
• MyVariant Identifiers: chr19:g.8645780G>T (hg19) ; chr19:g.8580896G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580896G>T , CM000681.2:g.8580896G>T	GRCh38
NC_000019.9:g.8645780G>T , CM000681.1:g.8645780G>T	GRCh37
NC_000019.8:g.8551780G>T	NCBI36
NG_011840.2:g.34807C>A
NG_052844.1:g.1552C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3309C>A MANE Select	ENSP00000471851.1:p.His1103Gln
ENST00000270328.8:c.3309C>A	ENSP00000270328.4:p.His1103Gln
ENST00000593913.5:c.*2186C>A	ENSP00000469901.1:n.*2186C>A
ENST00000595838.5:c.1770C>A	ENSP00000470501.1:p.His590Gln
ENST00000597188.5:c.3309C>A	ENSP00000471851.1:p.His1103Gln
NM_001282352.1:c.1770C>A	NP_001269281.1:p.His590Gln
NM_030957.3:c.3309C>A	NP_112219.3:p.His1103Gln
XM_006722917.2:c.2352C>A	XP_006722980.1:p.His784Gln
XM_011528331.1:c.3456C>A	XP_011526633.1:p.His1152Gln
XM_011528332.1:c.3456C>A	XP_011526634.1:p.His1152Gln
XM_011528333.1:c.3456C>A	XP_011526635.1:p.His1152Gln
XM_011528334.1:c.3132C>A	XP_011526636.1:p.His1044Gln
XM_011528335.1:c.2025C>A	XP_011526637.1:p.His675Gln
XM_011528336.1:c.2019C>A	XP_011526638.1:p.His673Gln
XM_006722917.3:c.2352C>A	XP_006722980.1:p.His784Gln
XM_017027338.2:c.3309C>A	XP_016882827.1:p.His1103Gln
XM_017027339.1:c.1878C>A	XP_016882828.1:p.His626Gln
XM_017027340.1:c.1872C>A	XP_016882829.1:p.His624Gln
NM_030957.4:c.3309C>A MANE Select	NP_112219.3:p.His1103Gln
NM_001282352.2:c.1770C>A	NP_001269281.1:p.His590Gln