Canonical Allele Identifier: CA993272863
Gene: ADAMTS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8600732_8600733insCA , CM000681.2:g.8600732_8600733insCA GRCh38
NC_000019.9:g.8665616_8665617insCA , CM000681.1:g.8665616_8665617insCA GRCh37
NC_000019.8:g.8571616_8571617insCA NCBI36
NG_011840.2:g.14970_14971insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.810+195_810+196insTG MANE Select ENSP00000471851.1:n.810+195_810+196insTG
ENST00000270328.8:c.810+195_810+196insTG ENSP00000270328.4:n.810+195_810+196insTG
ENST00000593913.5:c.810+195_810+196insTG ENSP00000469901.1:n.810+195_810+196insTG
ENST00000596466.2:n.759+195_759+196insTG
ENST00000596709.5:n.894+195_894+196insTG
ENST00000596851.5:c.810+195_810+196insTG ENSP00000469559.1:n.810+195_810+196insTG
ENST00000597188.5:c.810+195_810+196insTG ENSP00000471851.1:n.810+195_810+196insTG
NM_030957.3:c.810+195_810+196insTG NP_112219.3:n.810+195_810+196insTG
XM_006722917.2:c.-300+195_-300+196insTG XP_006722980.1:n.-300+195_-300+196insTG
XM_011528331.1:c.810+195_810+196insTG XP_011526633.1:n.810+195_810+196insTG
XM_011528332.1:c.810+195_810+196insTG XP_011526634.1:n.810+195_810+196insTG
XM_011528333.1:c.810+195_810+196insTG XP_011526635.1:n.810+195_810+196insTG
XM_011528334.1:c.810+195_810+196insTG XP_011526636.1:n.810+195_810+196insTG
XR_430156.2:n.1086+195_1086+196insTG
XR_936208.1:n.1086+195_1086+196insTG
XR_936209.1:n.1086+195_1086+196insTG
XM_006722917.3:c.-300+195_-300+196insTG XP_006722980.1:n.-300+195_-300+196insTG
XM_017027338.2:c.810+195_810+196insTG XP_016882827.1:n.810+195_810+196insTG
XR_001753770.1:n.1646+195_1646+196insTG
NM_030957.4:c.810+195_810+196insTG MANE Select NP_112219.3:n.810+195_810+196insTG