Canonical Allele Identifier: CA403747884

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645829C>T (hg19) ; chr19:g.8580945C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580945C>T , CM000681.2:g.8580945C>T	GRCh38
NC_000019.9:g.8645829C>T , CM000681.1:g.8645829C>T	GRCh37
NC_000019.8:g.8551829C>T	NCBI36
NG_011840.2:g.34758G>A
NG_052844.1:g.1503G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3260G>A MANE Select	ENSP00000471851.1:p.Cys1087Tyr
ENST00000270328.8:c.3260G>A	ENSP00000270328.4:p.Cys1087Tyr
ENST00000593913.5:c.*2137G>A	ENSP00000469901.1:n.*2137G>A
ENST00000595838.5:c.1721G>A	ENSP00000470501.1:p.Cys574Tyr
ENST00000597188.5:c.3260G>A	ENSP00000471851.1:p.Cys1087Tyr
NM_001282352.1:c.1721G>A	NP_001269281.1:p.Cys574Tyr
NM_030957.3:c.3260G>A	NP_112219.3:p.Cys1087Tyr
XM_006722917.2:c.2303G>A	XP_006722980.1:p.Cys768Tyr
XM_011528331.1:c.3407G>A	XP_011526633.1:p.Cys1136Tyr
XM_011528332.1:c.3407G>A	XP_011526634.1:p.Cys1136Tyr
XM_011528333.1:c.3407G>A	XP_011526635.1:p.Cys1136Tyr
XM_011528334.1:c.3083G>A	XP_011526636.1:p.Cys1028Tyr
XM_011528335.1:c.1976G>A	XP_011526637.1:p.Cys659Tyr
XM_011528336.1:c.1970G>A	XP_011526638.1:p.Cys657Tyr
XM_006722917.3:c.2303G>A	XP_006722980.1:p.Cys768Tyr
XM_017027338.2:c.3260G>A	XP_016882827.1:p.Cys1087Tyr
XM_017027339.1:c.1829G>A	XP_016882828.1:p.Cys610Tyr
XM_017027340.1:c.1823G>A	XP_016882829.1:p.Cys608Tyr
NM_030957.4:c.3260G>A MANE Select	NP_112219.3:p.Cys1087Tyr
NM_001282352.2:c.1721G>A	NP_001269281.1:p.Cys574Tyr