Canonical Allele Identifier: CA403747773

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645784C>A (hg19) ; chr19:g.8580900C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580900C>A , CM000681.2:g.8580900C>A	GRCh38
NC_000019.9:g.8645784C>A , CM000681.1:g.8645784C>A	GRCh37
NC_000019.8:g.8551784C>A	NCBI36
NG_011840.2:g.34803G>T
NG_052844.1:g.1548G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3305G>T MANE Select	ENSP00000471851.1:p.Gly1102Val
ENST00000270328.8:c.3305G>T	ENSP00000270328.4:p.Gly1102Val
ENST00000593913.5:c.*2182G>T	ENSP00000469901.1:n.*2182G>T
ENST00000595838.5:c.1766G>T	ENSP00000470501.1:p.Gly589Val
ENST00000597188.5:c.3305G>T	ENSP00000471851.1:p.Gly1102Val
NM_001282352.1:c.1766G>T	NP_001269281.1:p.Gly589Val
NM_030957.3:c.3305G>T	NP_112219.3:p.Gly1102Val
XM_006722917.2:c.2348G>T	XP_006722980.1:p.Gly783Val
XM_011528331.1:c.3452G>T	XP_011526633.1:p.Gly1151Val
XM_011528332.1:c.3452G>T	XP_011526634.1:p.Gly1151Val
XM_011528333.1:c.3452G>T	XP_011526635.1:p.Gly1151Val
XM_011528334.1:c.3128G>T	XP_011526636.1:p.Gly1043Val
XM_011528335.1:c.2021G>T	XP_011526637.1:p.Gly674Val
XM_011528336.1:c.2015G>T	XP_011526638.1:p.Gly672Val
XM_006722917.3:c.2348G>T	XP_006722980.1:p.Gly783Val
XM_017027338.2:c.3305G>T	XP_016882827.1:p.Gly1102Val
XM_017027339.1:c.1874G>T	XP_016882828.1:p.Gly625Val
XM_017027340.1:c.1868G>T	XP_016882829.1:p.Gly623Val
NM_030957.4:c.3305G>T MANE Select	NP_112219.3:p.Gly1102Val
NM_001282352.2:c.1766G>T	NP_001269281.1:p.Gly589Val