Canonical Allele Identifier: CA403747842

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645811C>G (hg19) ; chr19:g.8580927C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580927C>G , CM000681.2:g.8580927C>G	GRCh38
NC_000019.9:g.8645811C>G , CM000681.1:g.8645811C>G	GRCh37
NC_000019.8:g.8551811C>G	NCBI36
NG_011840.2:g.34776G>C
NG_052844.1:g.1521G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3278G>C MANE Select	ENSP00000471851.1:p.Arg1093Pro
ENST00000270328.8:c.3278G>C	ENSP00000270328.4:p.Arg1093Pro
ENST00000593913.5:c.*2155G>C	ENSP00000469901.1:n.*2155G>C
ENST00000595838.5:c.1739G>C	ENSP00000470501.1:p.Arg580Pro
ENST00000597188.5:c.3278G>C	ENSP00000471851.1:p.Arg1093Pro
NM_001282352.1:c.1739G>C	NP_001269281.1:p.Arg580Pro
NM_030957.3:c.3278G>C	NP_112219.3:p.Arg1093Pro
XM_006722917.2:c.2321G>C	XP_006722980.1:p.Arg774Pro
XM_011528331.1:c.3425G>C	XP_011526633.1:p.Arg1142Pro
XM_011528332.1:c.3425G>C	XP_011526634.1:p.Arg1142Pro
XM_011528333.1:c.3425G>C	XP_011526635.1:p.Arg1142Pro
XM_011528334.1:c.3101G>C	XP_011526636.1:p.Arg1034Pro
XM_011528335.1:c.1994G>C	XP_011526637.1:p.Arg665Pro
XM_011528336.1:c.1988G>C	XP_011526638.1:p.Arg663Pro
XM_006722917.3:c.2321G>C	XP_006722980.1:p.Arg774Pro
XM_017027338.2:c.3278G>C	XP_016882827.1:p.Arg1093Pro
XM_017027339.1:c.1847G>C	XP_016882828.1:p.Arg616Pro
XM_017027340.1:c.1841G>C	XP_016882829.1:p.Arg614Pro
NM_030957.4:c.3278G>C MANE Select	NP_112219.3:p.Arg1093Pro
NM_001282352.2:c.1739G>C	NP_001269281.1:p.Arg580Pro