Canonical Allele Identifier: CA403747942

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645853G>T (hg19) ; chr19:g.8580969G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580969G>T , CM000681.2:g.8580969G>T	GRCh38
NC_000019.9:g.8645853G>T , CM000681.1:g.8645853G>T	GRCh37
NC_000019.8:g.8551853G>T	NCBI36
NG_011840.2:g.34734C>A
NG_052844.1:g.1479C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3236C>A MANE Select	ENSP00000471851.1:p.Pro1079His
ENST00000270328.8:c.3236C>A	ENSP00000270328.4:p.Pro1079His
ENST00000593913.5:c.*2113C>A	ENSP00000469901.1:n.*2113C>A
ENST00000595838.5:c.1697C>A	ENSP00000470501.1:p.Pro566His
ENST00000597188.5:c.3236C>A	ENSP00000471851.1:p.Pro1079His
NM_001282352.1:c.1697C>A	NP_001269281.1:p.Pro566His
NM_030957.3:c.3236C>A	NP_112219.3:p.Pro1079His
XM_006722917.2:c.2279C>A	XP_006722980.1:p.Pro760His
XM_011528331.1:c.3383C>A	XP_011526633.1:p.Pro1128His
XM_011528332.1:c.3383C>A	XP_011526634.1:p.Pro1128His
XM_011528333.1:c.3383C>A	XP_011526635.1:p.Pro1128His
XM_011528334.1:c.3059C>A	XP_011526636.1:p.Pro1020His
XM_011528335.1:c.1952C>A	XP_011526637.1:p.Pro651His
XM_011528336.1:c.1946C>A	XP_011526638.1:p.Pro649His
XM_006722917.3:c.2279C>A	XP_006722980.1:p.Pro760His
XM_017027338.2:c.3236C>A	XP_016882827.1:p.Pro1079His
XM_017027339.1:c.1805C>A	XP_016882828.1:p.Pro602His
XM_017027340.1:c.1799C>A	XP_016882829.1:p.Pro600His
NM_030957.4:c.3236C>A MANE Select	NP_112219.3:p.Pro1079His
NM_001282352.2:c.1697C>A	NP_001269281.1:p.Pro566His