Canonical Allele Identifier: CA403747839

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645809G>C (hg19) ; chr19:g.8580925G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580925G>C , CM000681.2:g.8580925G>C	GRCh38
NC_000019.9:g.8645809G>C , CM000681.1:g.8645809G>C	GRCh37
NC_000019.8:g.8551809G>C	NCBI36
NG_011840.2:g.34778C>G
NG_052844.1:g.1523C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3280C>G MANE Select	ENSP00000471851.1:p.Gln1094Glu
ENST00000270328.8:c.3280C>G	ENSP00000270328.4:p.Gln1094Glu
ENST00000593913.5:c.*2157C>G	ENSP00000469901.1:n.*2157C>G
ENST00000595838.5:c.1741C>G	ENSP00000470501.1:p.Gln581Glu
ENST00000597188.5:c.3280C>G	ENSP00000471851.1:p.Gln1094Glu
NM_001282352.1:c.1741C>G	NP_001269281.1:p.Gln581Glu
NM_030957.3:c.3280C>G	NP_112219.3:p.Gln1094Glu
XM_006722917.2:c.2323C>G	XP_006722980.1:p.Gln775Glu
XM_011528331.1:c.3427C>G	XP_011526633.1:p.Gln1143Glu
XM_011528332.1:c.3427C>G	XP_011526634.1:p.Gln1143Glu
XM_011528333.1:c.3427C>G	XP_011526635.1:p.Gln1143Glu
XM_011528334.1:c.3103C>G	XP_011526636.1:p.Gln1035Glu
XM_011528335.1:c.1996C>G	XP_011526637.1:p.Gln666Glu
XM_011528336.1:c.1990C>G	XP_011526638.1:p.Gln664Glu
XM_006722917.3:c.2323C>G	XP_006722980.1:p.Gln775Glu
XM_017027338.2:c.3280C>G	XP_016882827.1:p.Gln1094Glu
XM_017027339.1:c.1849C>G	XP_016882828.1:p.Gln617Glu
XM_017027340.1:c.1843C>G	XP_016882829.1:p.Gln615Glu
NM_030957.4:c.3280C>G MANE Select	NP_112219.3:p.Gln1094Glu
NM_001282352.2:c.1741C>G	NP_001269281.1:p.Gln581Glu