Canonical Allele Identifier: CA2321504084
Gene: ADAMTS10 HGNC NCBI

Linked Data

dbSNP Id: rs6603092
gnomAD v4: 19-8600792-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8600792C>T , CM000681.2:g.8600792C>T GRCh38
NC_000019.9:g.8665676C>T , CM000681.1:g.8665676C>T GRCh37
NC_000019.8:g.8571676C>T NCBI36
NG_011840.2:g.14911G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000597188.6:c.810+136G>A MANE Select ENSP00000471851.1:n.810+136G>A
ENST00000270328.8:c.810+136G>A ENSP00000270328.4:n.810+136G>A
ENST00000593913.5:c.810+136G>A ENSP00000469901.1:n.810+136G>A
ENST00000596466.2:n.759+136G>A
ENST00000596709.5:n.894+136G>A
ENST00000596851.5:c.810+136G>A ENSP00000469559.1:n.810+136G>A
ENST00000597188.5:c.810+136G>A ENSP00000471851.1:n.810+136G>A
NM_030957.3:c.810+136G>A NP_112219.3:n.810+136G>A
XM_006722917.2:c.-300+136G>A XP_006722980.1:n.-300+136G>A
XM_011528331.1:c.810+136G>A XP_011526633.1:n.810+136G>A
XM_011528332.1:c.810+136G>A XP_011526634.1:n.810+136G>A
XM_011528333.1:c.810+136G>A XP_011526635.1:n.810+136G>A
XM_011528334.1:c.810+136G>A XP_011526636.1:n.810+136G>A
XR_430156.2:n.1086+136G>A
XR_936208.1:n.1086+136G>A
XR_936209.1:n.1086+136G>A
XM_006722917.3:c.-300+136G>A XP_006722980.1:n.-300+136G>A
XM_017027338.2:c.810+136G>A XP_016882827.1:n.810+136G>A
XR_001753770.1:n.1646+136G>A
NM_030957.4:c.810+136G>A MANE Select NP_112219.3:n.810+136G>A