Canonical Allele Identifier: CA2530464864
Gene: ADAMTS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8600904_8600905insAG , CM000681.2:g.8600904_8600905insAG GRCh38
NC_000019.9:g.8665788_8665789insAG , CM000681.1:g.8665788_8665789insAG GRCh37
NC_000019.8:g.8571788_8571789insAG NCBI36
NG_011840.2:g.14799_14800insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.810+24_810+25insTC MANE Select ENSP00000471851.1:n.810+24_810+25insTC
ENST00000270328.8:c.810+24_810+25insTC ENSP00000270328.4:n.810+24_810+25insTC
ENST00000593913.5:c.810+24_810+25insTC ENSP00000469901.1:n.810+24_810+25insTC
ENST00000596466.2:n.759+24_759+25insTC
ENST00000596709.5:n.894+24_894+25insTC
ENST00000596851.5:c.810+24_810+25insTC ENSP00000469559.1:n.810+24_810+25insTC
ENST00000597188.5:c.810+24_810+25insTC ENSP00000471851.1:n.810+24_810+25insTC
NM_030957.3:c.810+24_810+25insTC NP_112219.3:n.810+24_810+25insTC
XM_006722917.2:c.-300+24_-300+25insTC XP_006722980.1:n.-300+24_-300+25insTC
XM_011528331.1:c.810+24_810+25insTC XP_011526633.1:n.810+24_810+25insTC
XM_011528332.1:c.810+24_810+25insTC XP_011526634.1:n.810+24_810+25insTC
XM_011528333.1:c.810+24_810+25insTC XP_011526635.1:n.810+24_810+25insTC
XM_011528334.1:c.810+24_810+25insTC XP_011526636.1:n.810+24_810+25insTC
XR_430156.2:n.1086+24_1086+25insTC
XR_936208.1:n.1086+24_1086+25insTC
XR_936209.1:n.1086+24_1086+25insTC
XM_006722917.3:c.-300+24_-300+25insTC XP_006722980.1:n.-300+24_-300+25insTC
XM_017027338.2:c.810+24_810+25insTC XP_016882827.1:n.810+24_810+25insTC
XR_001753770.1:n.1646+24_1646+25insTC
NM_030957.4:c.810+24_810+25insTC MANE Select NP_112219.3:n.810+24_810+25insTC