Canonical Allele Identifier: CA2234468582
Gene: ADAMTS18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77396697_77396699delinsAAC , CM000678.2:g.77396697_77396699delinsAAC GRCh38
NC_000016.9:g.77430594_77430596delinsAAC , CM000678.1:g.77430594_77430596delinsAAC GRCh37
NC_000016.8:g.75988095_75988097delinsAAC NCBI36
NG_031879.1:g.43416_43418delinsGTT
NG_031879.2:g.43416_43418delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000282849.10:c.496-28976_496-28974delinsGTT MANE Select ENSP00000282849.5:n.496-28976_496-28974delinsGTT
ENST00000282849.9:c.496-28976_496-28974delinsGTT ENSP00000282849.5:n.496-28976_496-28974delinsGTT
ENST00000449265.2:c.496-28976_496-28974delinsGTT ENSP00000392540.2:n.496-28976_496-28974delinsGTT
ENST00000562345.1:c.294-29030_294-29028delinsGTT
ENST00000564369.1:n.422-28976_422-28974delinsGTT
ENST00000567121.5:n.353-28976_353-28974delinsGTT
ENST00000567914.1:n.340-28976_340-28974delinsGTT
ENST00000569309.1:n.453-17720_453-17718delinsGTT
NM_199355.2:c.496-28976_496-28974delinsGTT NP_955387.1:n.496-28976_496-28974delinsGTT
XM_011522923.1:c.-25-28976_-25-28974delinsGTT XP_011521225.1:n.-25-28976_-25-28974delinsGTT
XM_011522924.1:c.-25-28976_-25-28974delinsGTT XP_011521226.1:n.-25-28976_-25-28974delinsGTT
NM_001326358.1:c.-25-28976_-25-28974delinsGTT NP_001313287.1:n.-25-28976_-25-28974delinsGTT
NM_199355.3:c.496-28976_496-28974delinsGTT NP_955387.1:n.496-28976_496-28974delinsGTT
XM_011522924.2:c.-25-28976_-25-28974delinsGTT XP_011521226.1:n.-25-28976_-25-28974delinsGTT
XM_017022988.2:c.-585-28976_-585-28974delinsGTT XP_016878477.1:n.-585-28976_-585-28974delinsGTT
XM_017022989.1:c.-581-28976_-581-28974delinsGTT XP_016878478.1:n.-581-28976_-581-28974delinsGTT
NM_199355.4:c.496-28976_496-28974delinsGTT MANE Select NP_955387.1:n.496-28976_496-28974delinsGTT
NM_001326358.2:c.-25-28976_-25-28974delinsGTT NP_001313287.1:n.-25-28976_-25-28974delinsGTT