Canonical Allele Identifier: CA403747936

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645848C>T (hg19) ; chr19:g.8580964C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580964C>T , CM000681.2:g.8580964C>T	GRCh38
NC_000019.9:g.8645848C>T , CM000681.1:g.8645848C>T	GRCh37
NC_000019.8:g.8551848C>T	NCBI36
NG_011840.2:g.34739G>A
NG_052844.1:g.1484G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3241G>A MANE Select	ENSP00000471851.1:p.Val1081Met
ENST00000270328.8:c.3241G>A	ENSP00000270328.4:p.Val1081Met
ENST00000593913.5:c.*2118G>A	ENSP00000469901.1:n.*2118G>A
ENST00000595838.5:c.1702G>A	ENSP00000470501.1:p.Val568Met
ENST00000597188.5:c.3241G>A	ENSP00000471851.1:p.Val1081Met
NM_001282352.1:c.1702G>A	NP_001269281.1:p.Val568Met
NM_030957.3:c.3241G>A	NP_112219.3:p.Val1081Met
XM_006722917.2:c.2284G>A	XP_006722980.1:p.Val762Met
XM_011528331.1:c.3388G>A	XP_011526633.1:p.Val1130Met
XM_011528332.1:c.3388G>A	XP_011526634.1:p.Val1130Met
XM_011528333.1:c.3388G>A	XP_011526635.1:p.Val1130Met
XM_011528334.1:c.3064G>A	XP_011526636.1:p.Val1022Met
XM_011528335.1:c.1957G>A	XP_011526637.1:p.Val653Met
XM_011528336.1:c.1951G>A	XP_011526638.1:p.Val651Met
XM_006722917.3:c.2284G>A	XP_006722980.1:p.Val762Met
XM_017027338.2:c.3241G>A	XP_016882827.1:p.Val1081Met
XM_017027339.1:c.1810G>A	XP_016882828.1:p.Val604Met
XM_017027340.1:c.1804G>A	XP_016882829.1:p.Val602Met
NM_030957.4:c.3241G>A MANE Select	NP_112219.3:p.Val1081Met
NM_001282352.2:c.1702G>A	NP_001269281.1:p.Val568Met