Canonical Allele Identifier: CA505263064

Gene: ADAMTS10

Linked Data

• gnomAD v4: 19-8580938-T-A
• MyVariant Identifiers: chr19:g.8645822T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580938T>A , CM000681.2:g.8580938T>A	GRCh38
NC_000019.9:g.8645822T>A , CM000681.1:g.8645822T>A	GRCh37
NC_000019.8:g.8551822T>A	NCBI36
NG_011840.2:g.34765A>T
NG_052844.1:g.1510A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3267A>T MANE Select	ENSP00000471851.1:p.Arg1089=
ENST00000270328.8:c.3267A>T	ENSP00000270328.4:p.Arg1089=
ENST00000593913.5:c.*2144A>T	ENSP00000469901.1:n.*2144A>T
ENST00000595838.5:c.1728A>T	ENSP00000470501.1:p.Arg576=
ENST00000597188.5:c.3267A>T	ENSP00000471851.1:p.Arg1089=
NM_001282352.1:c.1728A>T	NP_001269281.1:p.Arg576=
NM_030957.3:c.3267A>T	NP_112219.3:p.Arg1089=
XM_006722917.2:c.2310A>T	XP_006722980.1:p.Arg770=
XM_011528331.1:c.3414A>T	XP_011526633.1:p.Arg1138=
XM_011528332.1:c.3414A>T	XP_011526634.1:p.Arg1138=
XM_011528333.1:c.3414A>T	XP_011526635.1:p.Arg1138=
XM_011528334.1:c.3090A>T	XP_011526636.1:p.Arg1030=
XM_011528335.1:c.1983A>T	XP_011526637.1:p.Arg661=
XM_011528336.1:c.1977A>T	XP_011526638.1:p.Arg659=
XM_006722917.3:c.2310A>T	XP_006722980.1:p.Arg770=
XM_017027338.2:c.3267A>T	XP_016882827.1:p.Arg1089=
XM_017027339.1:c.1836A>T	XP_016882828.1:p.Arg612=
XM_017027340.1:c.1830A>T	XP_016882829.1:p.Arg610=
NM_030957.4:c.3267A>T MANE Select	NP_112219.3:p.Arg1089=
NM_001282352.2:c.1728A>T	NP_001269281.1:p.Arg576=