Canonical Allele Identifier: CA505262921

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645798G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580914G>A , CM000681.2:g.8580914G>A	GRCh38
NC_000019.9:g.8645798G>A , CM000681.1:g.8645798G>A	GRCh37
NC_000019.8:g.8551798G>A	NCBI36
NG_011840.2:g.34789C>T
NG_052844.1:g.1534C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3291C>T MANE Select	ENSP00000471851.1:p.Cys1097=
ENST00000270328.8:c.3291C>T	ENSP00000270328.4:p.Cys1097=
ENST00000593913.5:c.*2168C>T	ENSP00000469901.1:n.*2168C>T
ENST00000595838.5:c.1752C>T	ENSP00000470501.1:p.Cys584=
ENST00000597188.5:c.3291C>T	ENSP00000471851.1:p.Cys1097=
NM_001282352.1:c.1752C>T	NP_001269281.1:p.Cys584=
NM_030957.3:c.3291C>T	NP_112219.3:p.Cys1097=
XM_006722917.2:c.2334C>T	XP_006722980.1:p.Cys778=
XM_011528331.1:c.3438C>T	XP_011526633.1:p.Cys1146=
XM_011528332.1:c.3438C>T	XP_011526634.1:p.Cys1146=
XM_011528333.1:c.3438C>T	XP_011526635.1:p.Cys1146=
XM_011528334.1:c.3114C>T	XP_011526636.1:p.Cys1038=
XM_011528335.1:c.2007C>T	XP_011526637.1:p.Cys669=
XM_011528336.1:c.2001C>T	XP_011526638.1:p.Cys667=
XM_006722917.3:c.2334C>T	XP_006722980.1:p.Cys778=
XM_017027338.2:c.3291C>T	XP_016882827.1:p.Cys1097=
XM_017027339.1:c.1860C>T	XP_016882828.1:p.Cys620=
XM_017027340.1:c.1854C>T	XP_016882829.1:p.Cys618=
NM_030957.4:c.3291C>T MANE Select	NP_112219.3:p.Cys1097=
NM_001282352.2:c.1752C>T	NP_001269281.1:p.Cys584=