Canonical Allele Identifier: CA505263196

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645843G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580959G>C , CM000681.2:g.8580959G>C	GRCh38
NC_000019.9:g.8645843G>C , CM000681.1:g.8645843G>C	GRCh37
NC_000019.8:g.8551843G>C	NCBI36
NG_011840.2:g.34744C>G
NG_052844.1:g.1489C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3246C>G MANE Select	ENSP00000471851.1:p.Leu1082=
ENST00000270328.8:c.3246C>G	ENSP00000270328.4:p.Leu1082=
ENST00000593913.5:c.*2123C>G	ENSP00000469901.1:n.*2123C>G
ENST00000595838.5:c.1707C>G	ENSP00000470501.1:p.Leu569=
ENST00000597188.5:c.3246C>G	ENSP00000471851.1:p.Leu1082=
NM_001282352.1:c.1707C>G	NP_001269281.1:p.Leu569=
NM_030957.3:c.3246C>G	NP_112219.3:p.Leu1082=
XM_006722917.2:c.2289C>G	XP_006722980.1:p.Leu763=
XM_011528331.1:c.3393C>G	XP_011526633.1:p.Leu1131=
XM_011528332.1:c.3393C>G	XP_011526634.1:p.Leu1131=
XM_011528333.1:c.3393C>G	XP_011526635.1:p.Leu1131=
XM_011528334.1:c.3069C>G	XP_011526636.1:p.Leu1023=
XM_011528335.1:c.1962C>G	XP_011526637.1:p.Leu654=
XM_011528336.1:c.1956C>G	XP_011526638.1:p.Leu652=
XM_006722917.3:c.2289C>G	XP_006722980.1:p.Leu763=
XM_017027338.2:c.3246C>G	XP_016882827.1:p.Leu1082=
XM_017027339.1:c.1815C>G	XP_016882828.1:p.Leu605=
XM_017027340.1:c.1809C>G	XP_016882829.1:p.Leu603=
NM_030957.4:c.3246C>G MANE Select	NP_112219.3:p.Leu1082=
NM_001282352.2:c.1707C>G	NP_001269281.1:p.Leu569=