Canonical Allele Identifier: CA2234468135
Gene: ADAMTS18 HGNC NCBI

Linked Data

dbSNP Id: rs2057256539

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77396331_77396348del , CM000678.2:g.77396331_77396348del GRCh38
NC_000016.9:g.77430228_77430245del , CM000678.1:g.77430228_77430245del GRCh37
NC_000016.8:g.75987729_75987746del NCBI36
NG_031879.1:g.43767_43784del
NG_031879.2:g.43767_43784del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282849.10:c.496-28625_496-28608del MANE Select ENSP00000282849.5:n.496-28625_496-28608del
ENST00000282849.9:c.496-28625_496-28608del ENSP00000282849.5:n.496-28625_496-28608del
ENST00000449265.2:c.496-28625_496-28608del ENSP00000392540.2:n.496-28625_496-28608del
ENST00000562345.1:c.294-28679_294-28662del
ENST00000564369.1:n.422-28625_422-28608del
ENST00000567121.5:n.353-28625_353-28608del
ENST00000567914.1:n.340-28625_340-28608del
ENST00000569309.1:n.453-17369_453-17352del
NM_199355.2:c.496-28625_496-28608del NP_955387.1:n.496-28625_496-28608del
XM_011522923.1:c.-25-28625_-25-28608del XP_011521225.1:n.-25-28625_-25-28608del
XM_011522924.1:c.-25-28625_-25-28608del XP_011521226.1:n.-25-28625_-25-28608del
NM_001326358.1:c.-25-28625_-25-28608del NP_001313287.1:n.-25-28625_-25-28608del
NM_199355.3:c.496-28625_496-28608del NP_955387.1:n.496-28625_496-28608del
XM_011522924.2:c.-25-28625_-25-28608del XP_011521226.1:n.-25-28625_-25-28608del
XM_017022988.2:c.-585-28625_-585-28608del XP_016878477.1:n.-585-28625_-585-28608del
XM_017022989.1:c.-581-28625_-581-28608del XP_016878478.1:n.-581-28625_-581-28608del
NM_199355.4:c.496-28625_496-28608del MANE Select NP_955387.1:n.496-28625_496-28608del
NM_001326358.2:c.-25-28625_-25-28608del NP_001313287.1:n.-25-28625_-25-28608del