Canonical Allele Identifier: CA403747932

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645847A>G (hg19) ; chr19:g.8580963A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580963A>G , CM000681.2:g.8580963A>G	GRCh38
NC_000019.9:g.8645847A>G , CM000681.1:g.8645847A>G	GRCh37
NC_000019.8:g.8551847A>G	NCBI36
NG_011840.2:g.34740T>C
NG_052844.1:g.1485T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3242T>C MANE Select	ENSP00000471851.1:p.Val1081Ala
ENST00000270328.8:c.3242T>C	ENSP00000270328.4:p.Val1081Ala
ENST00000593913.5:c.*2119T>C	ENSP00000469901.1:n.*2119T>C
ENST00000595838.5:c.1703T>C	ENSP00000470501.1:p.Val568Ala
ENST00000597188.5:c.3242T>C	ENSP00000471851.1:p.Val1081Ala
NM_001282352.1:c.1703T>C	NP_001269281.1:p.Val568Ala
NM_030957.3:c.3242T>C	NP_112219.3:p.Val1081Ala
XM_006722917.2:c.2285T>C	XP_006722980.1:p.Val762Ala
XM_011528331.1:c.3389T>C	XP_011526633.1:p.Val1130Ala
XM_011528332.1:c.3389T>C	XP_011526634.1:p.Val1130Ala
XM_011528333.1:c.3389T>C	XP_011526635.1:p.Val1130Ala
XM_011528334.1:c.3065T>C	XP_011526636.1:p.Val1022Ala
XM_011528335.1:c.1958T>C	XP_011526637.1:p.Val653Ala
XM_011528336.1:c.1952T>C	XP_011526638.1:p.Val651Ala
XM_006722917.3:c.2285T>C	XP_006722980.1:p.Val762Ala
XM_017027338.2:c.3242T>C	XP_016882827.1:p.Val1081Ala
XM_017027339.1:c.1811T>C	XP_016882828.1:p.Val604Ala
XM_017027340.1:c.1805T>C	XP_016882829.1:p.Val602Ala
NM_030957.4:c.3242T>C MANE Select	NP_112219.3:p.Val1081Ala
NM_001282352.2:c.1703T>C	NP_001269281.1:p.Val568Ala