Canonical Allele Identifier: CA10652342

Gene: ADAMTS10

Linked Data

• ClinVar Variation Id: 330570
• ClinVar RCV Id: RCV000383937
• dbSNP Id: rs886054707
• gnomAD v3: 19-8580482-G-A
• gnomAD v4: 19-8580482-G-A
• MyVariant Identifiers: chr19:g.8645366G>A (hg19) ; chr19:g.8580482G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580482G>A , CM000681.2:g.8580482G>A	GRCh38
NC_000019.9:g.8645366G>A , CM000681.1:g.8645366G>A	GRCh37
NC_000019.8:g.8551366G>A	NCBI36
NG_011840.2:g.35221C>T
NG_052844.1:g.1966C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.*411C>T MANE Select	ENSP00000471851.1:n.*411C>T
ENST00000270328.8:c.*411C>T	ENSP00000270328.4:n.*411C>T
ENST00000595838.5:c.*411C>T	ENSP00000470501.1:n.*411C>T
NM_001282352.1:c.*411C>T	NP_001269281.1:n.*411C>T
NM_030957.3:c.*411C>T	NP_112219.3:n.*411C>T
XM_006722917.2:c.*411C>T	XP_006722980.1:n.*411C>T
XM_011528331.1:c.*411C>T	XP_011526633.1:n.*411C>T
XM_011528332.1:c.*411C>T	XP_011526634.1:n.*411C>T
XM_011528333.1:c.*411C>T	XP_011526635.1:n.*411C>T
XM_011528334.1:c.*411C>T	XP_011526636.1:n.*411C>T
XM_011528335.1:c.*411C>T	XP_011526637.1:n.*411C>T
XM_011528336.1:c.*411C>T	XP_011526638.1:n.*411C>T
XM_006722917.3:c.*411C>T	XP_006722980.1:n.*411C>T
XM_017027339.1:c.*411C>T	XP_016882828.1:n.*411C>T
XM_017027340.1:c.*411C>T	XP_016882829.1:n.*411C>T
NM_030957.4:c.*411C>T MANE Select	NP_112219.3:n.*411C>T
NM_001282352.2:c.*411C>T	NP_001269281.1:n.*411C>T