Canonical Allele Identifier: CA304996231

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs957733790
• gnomAD v2: 19-8645331-T-C
• gnomAD v3: 19-8580447-T-C
• gnomAD v4: 19-8580447-T-C
• MyVariant Identifiers: chr19:g.8645331T>C (hg19) ; chr19:g.8580447T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580447T>C , CM000681.2:g.8580447T>C	GRCh38
NC_000019.9:g.8645331T>C , CM000681.1:g.8645331T>C	GRCh37
NC_000019.8:g.8551331T>C	NCBI36
NG_011840.2:g.35256A>G
NG_052844.1:g.2001A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.*446A>G MANE Select	ENSP00000471851.1:n.*446A>G
ENST00000270328.8:c.*446A>G	ENSP00000270328.4:n.*446A>G
ENST00000595838.5:c.*446A>G	ENSP00000470501.1:n.*446A>G
NM_001282352.1:c.*446A>G	NP_001269281.1:n.*446A>G
NM_030957.3:c.*446A>G	NP_112219.3:n.*446A>G
XM_006722917.2:c.*446A>G	XP_006722980.1:n.*446A>G
XM_011528331.1:c.*446A>G	XP_011526633.1:n.*446A>G
XM_011528332.1:c.*446A>G	XP_011526634.1:n.*446A>G
XM_011528333.1:c.*446A>G	XP_011526635.1:n.*446A>G
XM_011528334.1:c.*446A>G	XP_011526636.1:n.*446A>G
XM_011528335.1:c.*446A>G	XP_011526637.1:n.*446A>G
XM_011528336.1:c.*446A>G	XP_011526638.1:n.*446A>G
XM_006722917.3:c.*446A>G	XP_006722980.1:n.*446A>G
XM_017027339.1:c.*446A>G	XP_016882828.1:n.*446A>G
XM_017027340.1:c.*446A>G	XP_016882829.1:n.*446A>G
NM_030957.4:c.*446A>G MANE Select	NP_112219.3:n.*446A>G
NM_001282352.2:c.*446A>G	NP_001269281.1:n.*446A>G