Canonical Allele Identifier: CA2234465039

Gene: ADAMTS18

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77393649_77393651delinsAAG , CM000678.2:g.77393649_77393651delinsAAG	GRCh38
NC_000016.9:g.77427546_77427548delinsAAG , CM000678.1:g.77427546_77427548delinsAAG	GRCh37
NC_000016.8:g.75985047_75985049delinsAAG	NCBI36
NG_031879.1:g.46464_46466delinsCTT
NG_031879.2:g.46464_46466delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.496-25928_496-25926delinsCTT MANE Select	ENSP00000282849.5:n.496-25928_496-25926delinsCTT
ENST00000282849.9:c.496-25928_496-25926delinsCTT	ENSP00000282849.5:n.496-25928_496-25926delinsCTT
ENST00000449265.2:c.496-25928_496-25926delinsCTT	ENSP00000392540.2:n.496-25928_496-25926delinsCTT
ENST00000562345.1:c.294-25982_294-25980delinsCTT
ENST00000564369.1:n.422-25928_422-25926delinsCTT
ENST00000567121.5:n.353-25928_353-25926delinsCTT
ENST00000567914.1:n.340-25928_340-25926delinsCTT
ENST00000569309.1:n.453-14672_453-14670delinsCTT
NM_199355.2:c.496-25928_496-25926delinsCTT	NP_955387.1:n.496-25928_496-25926delinsCTT
XM_011522923.1:c.-25-25928_-25-25926delinsCTT	XP_011521225.1:n.-25-25928_-25-25926delinsCTT
XM_011522924.1:c.-25-25928_-25-25926delinsCTT	XP_011521226.1:n.-25-25928_-25-25926delinsCTT
NM_001326358.1:c.-25-25928_-25-25926delinsCTT	NP_001313287.1:n.-25-25928_-25-25926delinsCTT
NM_199355.3:c.496-25928_496-25926delinsCTT	NP_955387.1:n.496-25928_496-25926delinsCTT
XM_011522924.2:c.-25-25928_-25-25926delinsCTT	XP_011521226.1:n.-25-25928_-25-25926delinsCTT
XM_017022988.2:c.-585-25928_-585-25926delinsCTT	XP_016878477.1:n.-585-25928_-585-25926delinsCTT
XM_017022989.1:c.-581-25928_-581-25926delinsCTT	XP_016878478.1:n.-581-25928_-581-25926delinsCTT
NM_199355.4:c.496-25928_496-25926delinsCTT MANE Select	NP_955387.1:n.496-25928_496-25926delinsCTT
NM_001326358.2:c.-25-25928_-25-25926delinsCTT	NP_001313287.1:n.-25-25928_-25-25926delinsCTT