Canonical Allele Identifier: CA884336996

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs1172707707
• gnomAD v4: 19-8580502-T-G
• MyVariant Identifiers: chr19:g.8580502T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580502T>G , CM000681.2:g.8580502T>G	GRCh38
NC_000019.9:g.8645386T>G , CM000681.1:g.8645386T>G	GRCh37
NC_000019.8:g.8551386T>G	NCBI36
NG_011840.2:g.35201A>C
NG_052844.1:g.1946A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.*391A>C MANE Select	ENSP00000471851.1:n.*391A>C
ENST00000270328.8:c.*391A>C	ENSP00000270328.4:n.*391A>C
ENST00000595838.5:c.*391A>C	ENSP00000470501.1:n.*391A>C
NM_001282352.1:c.*391A>C	NP_001269281.1:n.*391A>C
NM_030957.3:c.*391A>C	NP_112219.3:n.*391A>C
XM_006722917.2:c.*391A>C	XP_006722980.1:n.*391A>C
XM_011528331.1:c.*391A>C	XP_011526633.1:n.*391A>C
XM_011528332.1:c.*391A>C	XP_011526634.1:n.*391A>C
XM_011528333.1:c.*391A>C	XP_011526635.1:n.*391A>C
XM_011528334.1:c.*391A>C	XP_011526636.1:n.*391A>C
XM_011528335.1:c.*391A>C	XP_011526637.1:n.*391A>C
XM_011528336.1:c.*391A>C	XP_011526638.1:n.*391A>C
XM_006722917.3:c.*391A>C	XP_006722980.1:n.*391A>C
XM_017027339.1:c.*391A>C	XP_016882828.1:n.*391A>C
XM_017027340.1:c.*391A>C	XP_016882829.1:n.*391A>C
NM_030957.4:c.*391A>C MANE Select	NP_112219.3:n.*391A>C
NM_001282352.2:c.*391A>C	NP_001269281.1:n.*391A>C