Canonical Allele Identifier: CA631364676

Gene: ADAMTS10

Linked Data

• ClinVar Variation Id: 893575
• ClinVar RCV Id: RCV001132070
• dbSNP Id: rs1302375936
• gnomAD v2: 19-8645447-T-A
• gnomAD v3: 19-8580563-T-A
• gnomAD v4: 19-8580563-T-A
• MyVariant Identifiers: chr19:g.8645447T>A (hg19) ; chr19:g.8580563T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580563T>A , CM000681.2:g.8580563T>A	GRCh38
NC_000019.9:g.8645447T>A , CM000681.1:g.8645447T>A	GRCh37
NC_000019.8:g.8551447T>A	NCBI36
NG_011840.2:g.35140A>T
NG_052844.1:g.1885A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.*330A>T MANE Select	ENSP00000471851.1:n.*330A>T
ENST00000270328.8:c.*330A>T	ENSP00000270328.4:n.*330A>T
ENST00000595838.5:c.*330A>T	ENSP00000470501.1:n.*330A>T
NM_001282352.1:c.*330A>T	NP_001269281.1:n.*330A>T
NM_030957.3:c.*330A>T	NP_112219.3:n.*330A>T
XM_006722917.2:c.*330A>T	XP_006722980.1:n.*330A>T
XM_011528331.1:c.*330A>T	XP_011526633.1:n.*330A>T
XM_011528332.1:c.*330A>T	XP_011526634.1:n.*330A>T
XM_011528333.1:c.*330A>T	XP_011526635.1:n.*330A>T
XM_011528334.1:c.*330A>T	XP_011526636.1:n.*330A>T
XM_011528335.1:c.*330A>T	XP_011526637.1:n.*330A>T
XM_011528336.1:c.*330A>T	XP_011526638.1:n.*330A>T
XM_006722917.3:c.*330A>T	XP_006722980.1:n.*330A>T
XM_017027339.1:c.*330A>T	XP_016882828.1:n.*330A>T
XM_017027340.1:c.*330A>T	XP_016882829.1:n.*330A>T
NM_030957.4:c.*330A>T MANE Select	NP_112219.3:n.*330A>T
NM_001282352.2:c.*330A>T	NP_001269281.1:n.*330A>T