Canonical Allele Identifier: CA403747788

Gene: ADAMTS10

Linked Data

• gnomAD v4: 19-8580906-C-A
• MyVariant Identifiers: chr19:g.8645790C>A (hg19) ; chr19:g.8580906C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580906C>A , CM000681.2:g.8580906C>A	GRCh38
NC_000019.9:g.8645790C>A , CM000681.1:g.8645790C>A	GRCh37
NC_000019.8:g.8551790C>A	NCBI36
NG_011840.2:g.34797G>T
NG_052844.1:g.1542G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3299G>T MANE Select	ENSP00000471851.1:p.Cys1100Phe
ENST00000270328.8:c.3299G>T	ENSP00000270328.4:p.Cys1100Phe
ENST00000593913.5:c.*2176G>T	ENSP00000469901.1:n.*2176G>T
ENST00000595838.5:c.1760G>T	ENSP00000470501.1:p.Cys587Phe
ENST00000597188.5:c.3299G>T	ENSP00000471851.1:p.Cys1100Phe
NM_001282352.1:c.1760G>T	NP_001269281.1:p.Cys587Phe
NM_030957.3:c.3299G>T	NP_112219.3:p.Cys1100Phe
XM_006722917.2:c.2342G>T	XP_006722980.1:p.Cys781Phe
XM_011528331.1:c.3446G>T	XP_011526633.1:p.Cys1149Phe
XM_011528332.1:c.3446G>T	XP_011526634.1:p.Cys1149Phe
XM_011528333.1:c.3446G>T	XP_011526635.1:p.Cys1149Phe
XM_011528334.1:c.3122G>T	XP_011526636.1:p.Cys1041Phe
XM_011528335.1:c.2015G>T	XP_011526637.1:p.Cys672Phe
XM_011528336.1:c.2009G>T	XP_011526638.1:p.Cys670Phe
XM_006722917.3:c.2342G>T	XP_006722980.1:p.Cys781Phe
XM_017027338.2:c.3299G>T	XP_016882827.1:p.Cys1100Phe
XM_017027339.1:c.1868G>T	XP_016882828.1:p.Cys623Phe
XM_017027340.1:c.1862G>T	XP_016882829.1:p.Cys621Phe
NM_030957.4:c.3299G>T MANE Select	NP_112219.3:p.Cys1100Phe
NM_001282352.2:c.1760G>T	NP_001269281.1:p.Cys587Phe