Canonical Allele Identifier: CA505263021

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645816G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580932G>A , CM000681.2:g.8580932G>A	GRCh38
NC_000019.9:g.8645816G>A , CM000681.1:g.8645816G>A	GRCh37
NC_000019.8:g.8551816G>A	NCBI36
NG_011840.2:g.34771C>T
NG_052844.1:g.1516C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3273C>T MANE Select	ENSP00000471851.1:p.Tyr1091=
ENST00000270328.8:c.3273C>T	ENSP00000270328.4:p.Tyr1091=
ENST00000593913.5:c.*2150C>T	ENSP00000469901.1:n.*2150C>T
ENST00000595838.5:c.1734C>T	ENSP00000470501.1:p.Tyr578=
ENST00000597188.5:c.3273C>T	ENSP00000471851.1:p.Tyr1091=
NM_001282352.1:c.1734C>T	NP_001269281.1:p.Tyr578=
NM_030957.3:c.3273C>T	NP_112219.3:p.Tyr1091=
XM_006722917.2:c.2316C>T	XP_006722980.1:p.Tyr772=
XM_011528331.1:c.3420C>T	XP_011526633.1:p.Tyr1140=
XM_011528332.1:c.3420C>T	XP_011526634.1:p.Tyr1140=
XM_011528333.1:c.3420C>T	XP_011526635.1:p.Tyr1140=
XM_011528334.1:c.3096C>T	XP_011526636.1:p.Tyr1032=
XM_011528335.1:c.1989C>T	XP_011526637.1:p.Tyr663=
XM_011528336.1:c.1983C>T	XP_011526638.1:p.Tyr661=
XM_006722917.3:c.2316C>T	XP_006722980.1:p.Tyr772=
XM_017027338.2:c.3273C>T	XP_016882827.1:p.Tyr1091=
XM_017027339.1:c.1842C>T	XP_016882828.1:p.Tyr614=
XM_017027340.1:c.1836C>T	XP_016882829.1:p.Tyr612=
NM_030957.4:c.3273C>T MANE Select	NP_112219.3:p.Tyr1091=
NM_001282352.2:c.1734C>T	NP_001269281.1:p.Tyr578=