Canonical Allele Identifier: CA2234465022

Gene: ADAMTS18

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77393623_77393626delinsCAAG , CM000678.2:g.77393623_77393626delinsCAAG	GRCh38
NC_000016.9:g.77427520_77427523delinsCAAG , CM000678.1:g.77427520_77427523delinsCAAG	GRCh37
NC_000016.8:g.75985021_75985024delinsCAAG	NCBI36
NG_031879.1:g.46489_46492delinsCTTG
NG_031879.2:g.46489_46492delinsCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.496-25903_496-25900delinsCTTG MANE Select	ENSP00000282849.5:n.496-25903_496-25900delinsCTTG
ENST00000282849.9:c.496-25903_496-25900delinsCTTG	ENSP00000282849.5:n.496-25903_496-25900delinsCTTG
ENST00000449265.2:c.496-25903_496-25900delinsCTTG	ENSP00000392540.2:n.496-25903_496-25900delinsCTTG
ENST00000562345.1:c.294-25957_294-25954delinsCTTG
ENST00000564369.1:n.422-25903_422-25900delinsCTTG
ENST00000567121.5:n.353-25903_353-25900delinsCTTG
ENST00000567914.1:n.340-25903_340-25900delinsCTTG
ENST00000569309.1:n.453-14647_453-14644delinsCTTG
NM_199355.2:c.496-25903_496-25900delinsCTTG	NP_955387.1:n.496-25903_496-25900delinsCTTG
XM_011522923.1:c.-25-25903_-25-25900delinsCTTG	XP_011521225.1:n.-25-25903_-25-25900delinsCTTG
XM_011522924.1:c.-25-25903_-25-25900delinsCTTG	XP_011521226.1:n.-25-25903_-25-25900delinsCTTG
NM_001326358.1:c.-25-25903_-25-25900delinsCTTG	NP_001313287.1:n.-25-25903_-25-25900delinsCTTG
NM_199355.3:c.496-25903_496-25900delinsCTTG	NP_955387.1:n.496-25903_496-25900delinsCTTG
XM_011522924.2:c.-25-25903_-25-25900delinsCTTG	XP_011521226.1:n.-25-25903_-25-25900delinsCTTG
XM_017022988.2:c.-585-25903_-585-25900delinsCTTG	XP_016878477.1:n.-585-25903_-585-25900delinsCTTG
XM_017022989.1:c.-581-25903_-581-25900delinsCTTG	XP_016878478.1:n.-581-25903_-581-25900delinsCTTG
NM_199355.4:c.496-25903_496-25900delinsCTTG MANE Select	NP_955387.1:n.496-25903_496-25900delinsCTTG
NM_001326358.2:c.-25-25903_-25-25900delinsCTTG	NP_001313287.1:n.-25-25903_-25-25900delinsCTTG