Canonical Allele Identifier: CA9159936

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs782483131
• ExAC: 19:8645772 GCC / G
• gnomAD v4: 19-8580888-GCC-G
• MyVariant Identifiers: chr19:g.8645773_8645774del (hg19) ; chr19:g.8580889_8580890del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580892_8580893del , CM000681.2:g.8580892_8580893del	GRCh38
NC_000019.9:g.8645776_8645777del , CM000681.1:g.8645776_8645777del	GRCh37
NC_000019.8:g.8551776_8551777del	NCBI36
NG_011840.2:g.34813_34814del
NG_052844.1:g.1558_1559del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.*3_*4del MANE Select	ENSP00000471851.1:n.*3_*4del
ENST00000270328.8:c.*3_*4del	ENSP00000270328.4:n.*3_*4del
ENST00000593913.5:c.*2192_*2193del	ENSP00000469901.1:n.*2192_*2193del
ENST00000595838.5:c.*3_*4del	ENSP00000470501.1:n.*3_*4del
ENST00000597188.5:c.*3_*4del	ENSP00000471851.1:n.*3_*4del
NM_001282352.1:c.*3_*4del	NP_001269281.1:n.*3_*4del
NM_030957.3:c.*3_*4del	NP_112219.3:n.*3_*4del
XM_006722917.2:c.*3_*4del	XP_006722980.1:n.*3_*4del
XM_011528331.1:c.*3_*4del	XP_011526633.1:n.*3_*4del
XM_011528332.1:c.*3_*4del	XP_011526634.1:n.*3_*4del
XM_011528333.1:c.*3_*4del	XP_011526635.1:n.*3_*4del
XM_011528334.1:c.*3_*4del	XP_011526636.1:n.*3_*4del
XM_011528335.1:c.*3_*4del	XP_011526637.1:n.*3_*4del
XM_011528336.1:c.*3_*4del	XP_011526638.1:n.*3_*4del
XM_006722917.3:c.*3_*4del	XP_006722980.1:n.*3_*4del
XM_017027338.2:c.*3_*4del	XP_016882827.1:n.*3_*4del
XM_017027339.1:c.*3_*4del	XP_016882828.1:n.*3_*4del
XM_017027340.1:c.*3_*4del	XP_016882829.1:n.*3_*4del
NM_030957.4:c.*3_*4del MANE Select	NP_112219.3:n.*3_*4del
NM_001282352.2:c.*3_*4del	NP_001269281.1:n.*3_*4del