Canonical Allele Identifier: CA403747768

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645781T>C (hg19) ; chr19:g.8580897T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580897T>C , CM000681.2:g.8580897T>C	GRCh38
NC_000019.9:g.8645781T>C , CM000681.1:g.8645781T>C	GRCh37
NC_000019.8:g.8551781T>C	NCBI36
NG_011840.2:g.34806A>G
NG_052844.1:g.1551A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3308A>G MANE Select	ENSP00000471851.1:p.His1103Arg
ENST00000270328.8:c.3308A>G	ENSP00000270328.4:p.His1103Arg
ENST00000593913.5:c.*2185A>G	ENSP00000469901.1:n.*2185A>G
ENST00000595838.5:c.1769A>G	ENSP00000470501.1:p.His590Arg
ENST00000597188.5:c.3308A>G	ENSP00000471851.1:p.His1103Arg
NM_001282352.1:c.1769A>G	NP_001269281.1:p.His590Arg
NM_030957.3:c.3308A>G	NP_112219.3:p.His1103Arg
XM_006722917.2:c.2351A>G	XP_006722980.1:p.His784Arg
XM_011528331.1:c.3455A>G	XP_011526633.1:p.His1152Arg
XM_011528332.1:c.3455A>G	XP_011526634.1:p.His1152Arg
XM_011528333.1:c.3455A>G	XP_011526635.1:p.His1152Arg
XM_011528334.1:c.3131A>G	XP_011526636.1:p.His1044Arg
XM_011528335.1:c.2024A>G	XP_011526637.1:p.His675Arg
XM_011528336.1:c.2018A>G	XP_011526638.1:p.His673Arg
XM_006722917.3:c.2351A>G	XP_006722980.1:p.His784Arg
XM_017027338.2:c.3308A>G	XP_016882827.1:p.His1103Arg
XM_017027339.1:c.1877A>G	XP_016882828.1:p.His626Arg
XM_017027340.1:c.1871A>G	XP_016882829.1:p.His624Arg
NM_030957.4:c.3308A>G MANE Select	NP_112219.3:p.His1103Arg
NM_001282352.2:c.1769A>G	NP_001269281.1:p.His590Arg