Canonical Allele Identifier: CA403748079

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8649794C>A (hg19) ; chr19:g.8584910C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8584910C>A , CM000681.2:g.8584910C>A	GRCh38
NC_000019.9:g.8649794C>A , CM000681.1:g.8649794C>A	GRCh37
NC_000019.8:g.8555794C>A	NCBI36
NG_011840.2:g.30793G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.3187G>T MANE Select	ENSP00000471851.1:p.Gly1063Trp
ENST00000270328.8:c.3187G>T	ENSP00000270328.4:p.Gly1063Trp
ENST00000593913.5:c.*2064G>T	ENSP00000469901.1:n.*2064G>T
ENST00000595838.5:c.1648G>T	ENSP00000470501.1:p.Gly550Trp
ENST00000597188.5:c.3187G>T	ENSP00000471851.1:p.Gly1063Trp
NM_001282352.1:c.1648G>T	NP_001269281.1:p.Gly550Trp
NM_030957.3:c.3187G>T	NP_112219.3:p.Gly1063Trp
XM_006722917.2:c.2230G>T	XP_006722980.1:p.Gly744Trp
XM_011528331.1:c.3334G>T	XP_011526633.1:p.Gly1112Trp
XM_011528332.1:c.3334G>T	XP_011526634.1:p.Gly1112Trp
XM_011528333.1:c.3334G>T	XP_011526635.1:p.Gly1112Trp
XM_011528334.1:c.3010G>T	XP_011526636.1:p.Gly1004Trp
XM_011528335.1:c.1903G>T	XP_011526637.1:p.Gly635Trp
XM_011528336.1:c.1897G>T	XP_011526638.1:p.Gly633Trp
XM_006722917.3:c.2230G>T	XP_006722980.1:p.Gly744Trp
XM_017027338.2:c.3187G>T	XP_016882827.1:p.Gly1063Trp
XM_017027339.1:c.1756G>T	XP_016882828.1:p.Gly586Trp
XM_017027340.1:c.1750G>T	XP_016882829.1:p.Gly584Trp
NM_030957.4:c.3187G>T MANE Select	NP_112219.3:p.Gly1063Trp
NM_001282352.2:c.1648G>T	NP_001269281.1:p.Gly550Trp