Canonical Allele Identifier: CA505262847

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs7252299
• gnomAD v2: 19-8645786-A-G
• gnomAD v3: 19-8580902-A-G
• gnomAD v4: 19-8580902-A-G
• MyVariant Identifiers: chr19:g.8645786A>G (hg19) ; chr19:g.8580902A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580902A>G , CM000681.2:g.8580902A>G	GRCh38
NC_000019.9:g.8645786A>G , CM000681.1:g.8645786A>G	GRCh37
NC_000019.8:g.8551786A>G	NCBI36
NG_011840.2:g.34801T>C
NG_052844.1:g.1546T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3303T>C MANE Select	ENSP00000471851.1:p.His1101=
ENST00000270328.8:c.3303T>C	ENSP00000270328.4:p.His1101=
ENST00000593913.5:c.*2180T>C	ENSP00000469901.1:n.*2180T>C
ENST00000595838.5:c.1764T>C	ENSP00000470501.1:p.His588=
ENST00000597188.5:c.3303T>C	ENSP00000471851.1:p.His1101=
NM_001282352.1:c.1764T>C	NP_001269281.1:p.His588=
NM_030957.3:c.3303T>C	NP_112219.3:p.His1101=
XM_006722917.2:c.2346T>C	XP_006722980.1:p.His782=
XM_011528331.1:c.3450T>C	XP_011526633.1:p.His1150=
XM_011528332.1:c.3450T>C	XP_011526634.1:p.His1150=
XM_011528333.1:c.3450T>C	XP_011526635.1:p.His1150=
XM_011528334.1:c.3126T>C	XP_011526636.1:p.His1042=
XM_011528335.1:c.2019T>C	XP_011526637.1:p.His673=
XM_011528336.1:c.2013T>C	XP_011526638.1:p.His671=
XM_006722917.3:c.2346T>C	XP_006722980.1:p.His782=
XM_017027338.2:c.3303T>C	XP_016882827.1:p.His1101=
XM_017027339.1:c.1872T>C	XP_016882828.1:p.His624=
XM_017027340.1:c.1866T>C	XP_016882829.1:p.His622=
NM_030957.4:c.3303T>C MANE Select	NP_112219.3:p.His1101=
NM_001282352.2:c.1764T>C	NP_001269281.1:p.His588=