Canonical Allele Identifier: CA505263178

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645840T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580956T>C , CM000681.2:g.8580956T>C	GRCh38
NC_000019.9:g.8645840T>C , CM000681.1:g.8645840T>C	GRCh37
NC_000019.8:g.8551840T>C	NCBI36
NG_011840.2:g.34747A>G
NG_052844.1:g.1492A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3249A>G MANE Select	ENSP00000471851.1:p.Lys1083=
ENST00000270328.8:c.3249A>G	ENSP00000270328.4:p.Lys1083=
ENST00000593913.5:c.*2126A>G	ENSP00000469901.1:n.*2126A>G
ENST00000595838.5:c.1710A>G	ENSP00000470501.1:p.Lys570=
ENST00000597188.5:c.3249A>G	ENSP00000471851.1:p.Lys1083=
NM_001282352.1:c.1710A>G	NP_001269281.1:p.Lys570=
NM_030957.3:c.3249A>G	NP_112219.3:p.Lys1083=
XM_006722917.2:c.2292A>G	XP_006722980.1:p.Lys764=
XM_011528331.1:c.3396A>G	XP_011526633.1:p.Lys1132=
XM_011528332.1:c.3396A>G	XP_011526634.1:p.Lys1132=
XM_011528333.1:c.3396A>G	XP_011526635.1:p.Lys1132=
XM_011528334.1:c.3072A>G	XP_011526636.1:p.Lys1024=
XM_011528335.1:c.1965A>G	XP_011526637.1:p.Lys655=
XM_011528336.1:c.1959A>G	XP_011526638.1:p.Lys653=
XM_006722917.3:c.2292A>G	XP_006722980.1:p.Lys764=
XM_017027338.2:c.3249A>G	XP_016882827.1:p.Lys1083=
XM_017027339.1:c.1818A>G	XP_016882828.1:p.Lys606=
XM_017027340.1:c.1812A>G	XP_016882829.1:p.Lys604=
NM_030957.4:c.3249A>G MANE Select	NP_112219.3:p.Lys1083=
NM_001282352.2:c.1710A>G	NP_001269281.1:p.Lys570=