Canonical Allele Identifier: CA403747828

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs1600087531
• MyVariant Identifiers: chr19:g.8645805A>G (hg19) ; chr19:g.8580921A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580921A>G , CM000681.2:g.8580921A>G	GRCh38
NC_000019.9:g.8645805A>G , CM000681.1:g.8645805A>G	GRCh37
NC_000019.8:g.8551805A>G	NCBI36
NG_011840.2:g.34782T>C
NG_052844.1:g.1527T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3284T>C MANE Select	ENSP00000471851.1:p.Met1095Thr
ENST00000270328.8:c.3284T>C	ENSP00000270328.4:p.Met1095Thr
ENST00000593913.5:c.*2161T>C	ENSP00000469901.1:n.*2161T>C
ENST00000595838.5:c.1745T>C	ENSP00000470501.1:p.Met582Thr
ENST00000597188.5:c.3284T>C	ENSP00000471851.1:p.Met1095Thr
NM_001282352.1:c.1745T>C	NP_001269281.1:p.Met582Thr
NM_030957.3:c.3284T>C	NP_112219.3:p.Met1095Thr
XM_006722917.2:c.2327T>C	XP_006722980.1:p.Met776Thr
XM_011528331.1:c.3431T>C	XP_011526633.1:p.Met1144Thr
XM_011528332.1:c.3431T>C	XP_011526634.1:p.Met1144Thr
XM_011528333.1:c.3431T>C	XP_011526635.1:p.Met1144Thr
XM_011528334.1:c.3107T>C	XP_011526636.1:p.Met1036Thr
XM_011528335.1:c.2000T>C	XP_011526637.1:p.Met667Thr
XM_011528336.1:c.1994T>C	XP_011526638.1:p.Met665Thr
XM_006722917.3:c.2327T>C	XP_006722980.1:p.Met776Thr
XM_017027338.2:c.3284T>C	XP_016882827.1:p.Met1095Thr
XM_017027339.1:c.1853T>C	XP_016882828.1:p.Met618Thr
XM_017027340.1:c.1847T>C	XP_016882829.1:p.Met616Thr
NM_030957.4:c.3284T>C MANE Select	NP_112219.3:p.Met1095Thr
NM_001282352.2:c.1745T>C	NP_001269281.1:p.Met582Thr