Canonical Allele Identifier: CA505262889

Gene: ADAMTS10

Linked Data

• gnomAD v4: 19-8580908-G-T
• MyVariant Identifiers: chr19:g.8645792G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580908G>T , CM000681.2:g.8580908G>T	GRCh38
NC_000019.9:g.8645792G>T , CM000681.1:g.8645792G>T	GRCh37
NC_000019.8:g.8551792G>T	NCBI36
NG_011840.2:g.34795C>A
NG_052844.1:g.1540C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3297C>A MANE Select	ENSP00000471851.1:p.Thr1099=
ENST00000270328.8:c.3297C>A	ENSP00000270328.4:p.Thr1099=
ENST00000593913.5:c.*2174C>A	ENSP00000469901.1:n.*2174C>A
ENST00000595838.5:c.1758C>A	ENSP00000470501.1:p.Thr586=
ENST00000597188.5:c.3297C>A	ENSP00000471851.1:p.Thr1099=
NM_001282352.1:c.1758C>A	NP_001269281.1:p.Thr586=
NM_030957.3:c.3297C>A	NP_112219.3:p.Thr1099=
XM_006722917.2:c.2340C>A	XP_006722980.1:p.Thr780=
XM_011528331.1:c.3444C>A	XP_011526633.1:p.Thr1148=
XM_011528332.1:c.3444C>A	XP_011526634.1:p.Thr1148=
XM_011528333.1:c.3444C>A	XP_011526635.1:p.Thr1148=
XM_011528334.1:c.3120C>A	XP_011526636.1:p.Thr1040=
XM_011528335.1:c.2013C>A	XP_011526637.1:p.Thr671=
XM_011528336.1:c.2007C>A	XP_011526638.1:p.Thr669=
XM_006722917.3:c.2340C>A	XP_006722980.1:p.Thr780=
XM_017027338.2:c.3297C>A	XP_016882827.1:p.Thr1099=
XM_017027339.1:c.1866C>A	XP_016882828.1:p.Thr622=
XM_017027340.1:c.1860C>A	XP_016882829.1:p.Thr620=
NM_030957.4:c.3297C>A MANE Select	NP_112219.3:p.Thr1099=
NM_001282352.2:c.1758C>A	NP_001269281.1:p.Thr586=