Canonical Allele Identifier: CA2588120936
Gene: ADAMTS10 HGNC NCBI

Linked Data

gnomAD v4: 19-8604946-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8604946G>C , CM000681.2:g.8604946G>C GRCh38
NC_000019.9:g.8669831G>C , CM000681.1:g.8669831G>C GRCh37
NC_000019.8:g.8575831G>C NCBI36
NG_011840.2:g.10757C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000597188.6:c.435+66C>G MANE Select ENSP00000471851.1:n.435+66C>G
ENST00000270328.8:c.435+66C>G ENSP00000270328.4:n.435+66C>G
ENST00000593534.1:n.620C>G
ENST00000593913.5:c.435+66C>G ENSP00000469901.1:n.435+66C>G
ENST00000596466.2:n.384+66C>G
ENST00000596709.5:n.519+66C>G
ENST00000596851.5:c.435+66C>G ENSP00000469559.1:n.435+66C>G
ENST00000597188.5:c.435+66C>G ENSP00000471851.1:n.435+66C>G
NM_030957.3:c.435+66C>G NP_112219.3:n.435+66C>G
XM_006722917.2:c.-675+66C>G XP_006722980.1:n.-675+66C>G
XM_011528331.1:c.435+66C>G XP_011526633.1:n.435+66C>G
XM_011528332.1:c.435+66C>G XP_011526634.1:n.435+66C>G
XM_011528333.1:c.435+66C>G XP_011526635.1:n.435+66C>G
XM_011528334.1:c.435+66C>G XP_011526636.1:n.435+66C>G
XR_430156.2:n.711+66C>G
XR_936208.1:n.711+66C>G
XR_936209.1:n.711+66C>G
XM_006722917.3:c.-675+66C>G XP_006722980.1:n.-675+66C>G
XM_017027338.2:c.435+66C>G XP_016882827.1:n.435+66C>G
XR_001753770.1:n.1271+66C>G
NM_030957.4:c.435+66C>G MANE Select NP_112219.3:n.435+66C>G