Canonical Allele Identifier: CA993272670
Gene: ADAMTS10 HGNC NCBI

Linked Data

dbSNP Id: rs2042656669

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8600654_8600655insTG , CM000681.2:g.8600654_8600655insTG GRCh38
NC_000019.9:g.8665538_8665539insTG , CM000681.1:g.8665538_8665539insTG GRCh37
NC_000019.8:g.8571538_8571539insTG NCBI36
NG_011840.2:g.15048_15049insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.810+273_810+274insCA MANE Select ENSP00000471851.1:n.810+273_810+274insCA
ENST00000270328.8:c.810+273_810+274insCA ENSP00000270328.4:n.810+273_810+274insCA
ENST00000593913.5:c.810+273_810+274insCA ENSP00000469901.1:n.810+273_810+274insCA
ENST00000596466.2:n.759+273_759+274insCA
ENST00000596709.5:n.894+273_894+274insCA
ENST00000596851.5:c.810+273_810+274insCA ENSP00000469559.1:n.810+273_810+274insCA
ENST00000597188.5:c.810+273_810+274insCA ENSP00000471851.1:n.810+273_810+274insCA
NM_030957.3:c.810+273_810+274insCA NP_112219.3:n.810+273_810+274insCA
XM_006722917.2:c.-300+273_-300+274insCA XP_006722980.1:n.-300+273_-300+274insCA
XM_011528331.1:c.810+273_810+274insCA XP_011526633.1:n.810+273_810+274insCA
XM_011528332.1:c.810+273_810+274insCA XP_011526634.1:n.810+273_810+274insCA
XM_011528333.1:c.810+273_810+274insCA XP_011526635.1:n.810+273_810+274insCA
XM_011528334.1:c.810+273_810+274insCA XP_011526636.1:n.810+273_810+274insCA
XR_430156.2:n.1086+273_1086+274insCA
XR_936208.1:n.1086+273_1086+274insCA
XR_936209.1:n.1086+273_1086+274insCA
XM_006722917.3:c.-300+273_-300+274insCA XP_006722980.1:n.-300+273_-300+274insCA
XM_017027338.2:c.810+273_810+274insCA XP_016882827.1:n.810+273_810+274insCA
XR_001753770.1:n.1646+273_1646+274insCA
NM_030957.4:c.810+273_810+274insCA MANE Select NP_112219.3:n.810+273_810+274insCA