Canonical Allele Identifier: CA9159935

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs781788129
• ExAC: 19:8645770 G / GCGC
• gnomAD v2: 19-8645770-G-GCGC
• gnomAD v3: 19-8580886-G-GCGC
• gnomAD v4: 19-8580886-G-GCGC
• MyVariant Identifiers: chr19:g.8645770_8645771insCGC (hg19) ; chr19:g.8580886_8580887insCGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580888_8580890dup , CM000681.2:g.8580888_8580890dup	GRCh38
NC_000019.9:g.8645772_8645774dup , CM000681.1:g.8645772_8645774dup	GRCh37
NC_000019.8:g.8551772_8551774dup	NCBI36
NG_011840.2:g.34814_34816dup
NG_052844.1:g.1559_1561dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.*4_*6dup MANE Select	ENSP00000471851.1:n.*4_*6dup
ENST00000270328.8:c.*4_*6dup	ENSP00000270328.4:n.*4_*6dup
ENST00000593913.5:c.*2193_*2195dup	ENSP00000469901.1:n.*2193_*2195dup
ENST00000595838.5:c.*4_*6dup	ENSP00000470501.1:n.*4_*6dup
ENST00000597188.5:c.*4_*6dup	ENSP00000471851.1:n.*4_*6dup
NM_001282352.1:c.*4_*6dup	NP_001269281.1:n.*4_*6dup
NM_030957.3:c.*4_*6dup	NP_112219.3:n.*4_*6dup
XM_006722917.2:c.*4_*6dup	XP_006722980.1:n.*4_*6dup
XM_011528331.1:c.*4_*6dup	XP_011526633.1:n.*4_*6dup
XM_011528332.1:c.*4_*6dup	XP_011526634.1:n.*4_*6dup
XM_011528333.1:c.*4_*6dup	XP_011526635.1:n.*4_*6dup
XM_011528334.1:c.*4_*6dup	XP_011526636.1:n.*4_*6dup
XM_011528335.1:c.*4_*6dup	XP_011526637.1:n.*4_*6dup
XM_011528336.1:c.*4_*6dup	XP_011526638.1:n.*4_*6dup
XM_006722917.3:c.*4_*6dup	XP_006722980.1:n.*4_*6dup
XM_017027338.2:c.*4_*6dup	XP_016882827.1:n.*4_*6dup
XM_017027339.1:c.*4_*6dup	XP_016882828.1:n.*4_*6dup
XM_017027340.1:c.*4_*6dup	XP_016882829.1:n.*4_*6dup
NM_030957.4:c.*4_*6dup MANE Select	NP_112219.3:n.*4_*6dup
NM_001282352.2:c.*4_*6dup	NP_001269281.1:n.*4_*6dup