Canonical Allele Identifier: CA979259161
Gene: ADAMTS18 HGNC NCBI

Linked Data

dbSNP Id: rs2057219612

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77393652_77393653del , CM000678.2:g.77393652_77393653del GRCh38
NC_000016.9:g.77427549_77427550del , CM000678.1:g.77427549_77427550del GRCh37
NC_000016.8:g.75985050_75985051del NCBI36
NG_031879.1:g.46464_46465del
NG_031879.2:g.46464_46465del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282849.10:c.496-25928_496-25927del MANE Select ENSP00000282849.5:n.496-25928_496-25927del
ENST00000282849.9:c.496-25928_496-25927del ENSP00000282849.5:n.496-25928_496-25927del
ENST00000449265.2:c.496-25928_496-25927del ENSP00000392540.2:n.496-25928_496-25927del
ENST00000562345.1:c.294-25982_294-25981del
ENST00000564369.1:n.422-25928_422-25927del
ENST00000567121.5:n.353-25928_353-25927del
ENST00000567914.1:n.340-25928_340-25927del
ENST00000569309.1:n.453-14672_453-14671del
NM_199355.2:c.496-25928_496-25927del NP_955387.1:n.496-25928_496-25927del
XM_011522923.1:c.-25-25928_-25-25927del XP_011521225.1:n.-25-25928_-25-25927del
XM_011522924.1:c.-25-25928_-25-25927del XP_011521226.1:n.-25-25928_-25-25927del
NM_001326358.1:c.-25-25928_-25-25927del NP_001313287.1:n.-25-25928_-25-25927del
NM_199355.3:c.496-25928_496-25927del NP_955387.1:n.496-25928_496-25927del
XM_011522924.2:c.-25-25928_-25-25927del XP_011521226.1:n.-25-25928_-25-25927del
XM_017022988.2:c.-585-25928_-585-25927del XP_016878477.1:n.-585-25928_-585-25927del
XM_017022989.1:c.-581-25928_-581-25927del XP_016878478.1:n.-581-25928_-581-25927del
NM_199355.4:c.496-25928_496-25927del MANE Select NP_955387.1:n.496-25928_496-25927del
NM_001326358.2:c.-25-25928_-25-25927del NP_001313287.1:n.-25-25928_-25-25927del