Canonical Allele Identifier: CA403748090

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8649800T>A (hg19) ; chr19:g.8584916T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8584916T>A , CM000681.2:g.8584916T>A	GRCh38
NC_000019.9:g.8649800T>A , CM000681.1:g.8649800T>A	GRCh37
NC_000019.8:g.8555800T>A	NCBI36
NG_011840.2:g.30787A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.3181A>T MANE Select	ENSP00000471851.1:p.Thr1061Ser
ENST00000270328.8:c.3181A>T	ENSP00000270328.4:p.Thr1061Ser
ENST00000593913.5:c.*2058A>T	ENSP00000469901.1:n.*2058A>T
ENST00000595838.5:c.1642A>T	ENSP00000470501.1:p.Thr548Ser
ENST00000597188.5:c.3181A>T	ENSP00000471851.1:p.Thr1061Ser
NM_001282352.1:c.1642A>T	NP_001269281.1:p.Thr548Ser
NM_030957.3:c.3181A>T	NP_112219.3:p.Thr1061Ser
XM_006722917.2:c.2224A>T	XP_006722980.1:p.Thr742Ser
XM_011528331.1:c.3328A>T	XP_011526633.1:p.Thr1110Ser
XM_011528332.1:c.3328A>T	XP_011526634.1:p.Thr1110Ser
XM_011528333.1:c.3328A>T	XP_011526635.1:p.Thr1110Ser
XM_011528334.1:c.3004A>T	XP_011526636.1:p.Thr1002Ser
XM_011528335.1:c.1897A>T	XP_011526637.1:p.Thr633Ser
XM_011528336.1:c.1891A>T	XP_011526638.1:p.Thr631Ser
XM_006722917.3:c.2224A>T	XP_006722980.1:p.Thr742Ser
XM_017027338.2:c.3181A>T	XP_016882827.1:p.Thr1061Ser
XM_017027339.1:c.1750A>T	XP_016882828.1:p.Thr584Ser
XM_017027340.1:c.1744A>T	XP_016882829.1:p.Thr582Ser
NM_030957.4:c.3181A>T MANE Select	NP_112219.3:p.Thr1061Ser
NM_001282352.2:c.1642A>T	NP_001269281.1:p.Thr548Ser