Canonical Allele Identifier: CA993272728
Gene: ADAMTS10 HGNC NCBI

Linked Data

dbSNP Id: rs1207766223

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8600679dup , CM000681.2:g.8600679dup GRCh38
NC_000019.9:g.8665563dup , CM000681.1:g.8665563dup GRCh37
NC_000019.8:g.8571563dup NCBI36
NG_011840.2:g.15028dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.810+253dup MANE Select ENSP00000471851.1:n.810+253dup
ENST00000270328.8:c.810+253dup ENSP00000270328.4:n.810+253dup
ENST00000593913.5:c.810+253dup ENSP00000469901.1:n.810+253dup
ENST00000596466.2:n.759+253dup
ENST00000596709.5:n.894+253dup
ENST00000596851.5:c.810+253dup ENSP00000469559.1:n.810+253dup
ENST00000597188.5:c.810+253dup ENSP00000471851.1:n.810+253dup
NM_030957.3:c.810+253dup NP_112219.3:n.810+253dup
XM_006722917.2:c.-300+253dup XP_006722980.1:n.-300+253dup
XM_011528331.1:c.810+253dup XP_011526633.1:n.810+253dup
XM_011528332.1:c.810+253dup XP_011526634.1:n.810+253dup
XM_011528333.1:c.810+253dup XP_011526635.1:n.810+253dup
XM_011528334.1:c.810+253dup XP_011526636.1:n.810+253dup
XR_430156.2:n.1086+253dup
XR_936208.1:n.1086+253dup
XR_936209.1:n.1086+253dup
XM_006722917.3:c.-300+253dup XP_006722980.1:n.-300+253dup
XM_017027338.2:c.810+253dup XP_016882827.1:n.810+253dup
XR_001753770.1:n.1646+253dup
NM_030957.4:c.810+253dup MANE Select NP_112219.3:n.810+253dup