Canonical Allele Identifier: CA403748076

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs1555736411
• gnomAD v2: 19-8649791-C-T
• gnomAD v3: 19-8584907-C-T
• gnomAD v4: 19-8584907-C-T
• MyVariant Identifiers: chr19:g.8649791C>T (hg19) ; chr19:g.8584907C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8584907C>T , CM000681.2:g.8584907C>T	GRCh38
NC_000019.9:g.8649791C>T , CM000681.1:g.8649791C>T	GRCh37
NC_000019.8:g.8555791C>T	NCBI36
NG_011840.2:g.30796G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.3190G>A MANE Select	ENSP00000471851.1:p.Asp1064Asn
ENST00000270328.8:c.3190G>A	ENSP00000270328.4:p.Asp1064Asn
ENST00000593913.5:c.*2067G>A	ENSP00000469901.1:n.*2067G>A
ENST00000595838.5:c.1651G>A	ENSP00000470501.1:p.Asp551Asn
ENST00000597188.5:c.3190G>A	ENSP00000471851.1:p.Asp1064Asn
NM_001282352.1:c.1651G>A	NP_001269281.1:p.Asp551Asn
NM_030957.3:c.3190G>A	NP_112219.3:p.Asp1064Asn
XM_006722917.2:c.2233G>A	XP_006722980.1:p.Asp745Asn
XM_011528331.1:c.3337G>A	XP_011526633.1:p.Asp1113Asn
XM_011528332.1:c.3337G>A	XP_011526634.1:p.Asp1113Asn
XM_011528333.1:c.3337G>A	XP_011526635.1:p.Asp1113Asn
XM_011528334.1:c.3013G>A	XP_011526636.1:p.Asp1005Asn
XM_011528335.1:c.1906G>A	XP_011526637.1:p.Asp636Asn
XM_011528336.1:c.1900G>A	XP_011526638.1:p.Asp634Asn
XM_006722917.3:c.2233G>A	XP_006722980.1:p.Asp745Asn
XM_017027338.2:c.3190G>A	XP_016882827.1:p.Asp1064Asn
XM_017027339.1:c.1759G>A	XP_016882828.1:p.Asp587Asn
XM_017027340.1:c.1753G>A	XP_016882829.1:p.Asp585Asn
NM_030957.4:c.3190G>A MANE Select	NP_112219.3:p.Asp1064Asn
NM_001282352.2:c.1651G>A	NP_001269281.1:p.Asp551Asn