Canonical Allele Identifier: CA2530130553

Gene: ADAMTS18

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77395179_77395181del , CM000678.2:g.77395179_77395181del	GRCh38
NC_000016.9:g.77429076_77429078del , CM000678.1:g.77429076_77429078del	GRCh37
NC_000016.8:g.75986577_75986579del	NCBI36
NG_031879.1:g.44938_44940del
NG_031879.2:g.44938_44940del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.496-27454_496-27452del MANE Select	ENSP00000282849.5:n.496-27454_496-27452del
ENST00000282849.9:c.496-27454_496-27452del	ENSP00000282849.5:n.496-27454_496-27452del
ENST00000449265.2:c.496-27454_496-27452del	ENSP00000392540.2:n.496-27454_496-27452del
ENST00000562345.1:c.294-27508_294-27506del
ENST00000564369.1:n.422-27454_422-27452del
ENST00000567121.5:n.353-27454_353-27452del
ENST00000567914.1:n.340-27454_340-27452del
ENST00000569309.1:n.453-16198_453-16196del
NM_199355.2:c.496-27454_496-27452del	NP_955387.1:n.496-27454_496-27452del
XM_011522923.1:c.-25-27454_-25-27452del	XP_011521225.1:n.-25-27454_-25-27452del
XM_011522924.1:c.-25-27454_-25-27452del	XP_011521226.1:n.-25-27454_-25-27452del
NM_001326358.1:c.-25-27454_-25-27452del	NP_001313287.1:n.-25-27454_-25-27452del
NM_199355.3:c.496-27454_496-27452del	NP_955387.1:n.496-27454_496-27452del
XM_011522924.2:c.-25-27454_-25-27452del	XP_011521226.1:n.-25-27454_-25-27452del
XM_017022988.2:c.-585-27454_-585-27452del	XP_016878477.1:n.-585-27454_-585-27452del
XM_017022989.1:c.-581-27454_-581-27452del	XP_016878478.1:n.-581-27454_-581-27452del
NM_199355.4:c.496-27454_496-27452del MANE Select	NP_955387.1:n.496-27454_496-27452del
NM_001326358.2:c.-25-27454_-25-27452del	NP_001313287.1:n.-25-27454_-25-27452del