Canonical Allele Identifier: CA2234468134

Gene: ADAMTS18

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77396330_77396348delinsAAGAAATTTATCAATATGG , CM000678.2:g.77396330_77396348delinsAAGAAATTTATCAATATGG	GRCh38
NC_000016.9:g.77430227_77430245delinsAAGAAATTTATCAATATGG , CM000678.1:g.77430227_77430245delinsAAGAAATTTATCAATATGG	GRCh37
NC_000016.8:g.75987728_75987746delinsAAGAAATTTATCAATATGG	NCBI36
NG_031879.1:g.43767_43785delinsCCATATTGATAAATTTCTT
NG_031879.2:g.43767_43785delinsCCATATTGATAAATTTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.496-28625_496-28607delinsCCATATTGATAAATTTCTT MANE Select	ENSP00000282849.5:n.496-28625_496-28607delinsCCATATTGATAAATTT...
ENST00000282849.9:c.496-28625_496-28607delinsCCATATTGATAAATTTCTT	ENSP00000282849.5:n.496-28625_496-28607delinsCCATATTGATAAATTT...
ENST00000449265.2:c.496-28625_496-28607delinsCCATATTGATAAATTTCTT	ENSP00000392540.2:n.496-28625_496-28607delinsCCATATTGATAAATTT...
ENST00000562345.1:c.294-28679_294-28661delinsCCATATTGATAAATTTCTT
ENST00000564369.1:n.422-28625_422-28607delinsCCATATTGATAAATTTCTT
ENST00000567121.5:n.353-28625_353-28607delinsCCATATTGATAAATTTCTT
ENST00000567914.1:n.340-28625_340-28607delinsCCATATTGATAAATTTCTT
ENST00000569309.1:n.453-17369_453-17351delinsCCATATTGATAAATTTCTT
NM_199355.2:c.496-28625_496-28607delinsCCATATTGATAAATTTCTT	NP_955387.1:n.496-28625_496-28607delinsCCATATTGATAAATTTCTT
XM_011522923.1:c.-25-28625_-25-28607delinsCCATATTGATAAATTTCTT	XP_011521225.1:n.-25-28625_-25-28607delinsCCATATTGATAAATTTCTT...
XM_011522924.1:c.-25-28625_-25-28607delinsCCATATTGATAAATTTCTT	XP_011521226.1:n.-25-28625_-25-28607delinsCCATATTGATAAATTTCTT...
NM_001326358.1:c.-25-28625_-25-28607delinsCCATATTGATAAATTTCTT	NP_001313287.1:n.-25-28625_-25-28607delinsCCATATTGATAAATTTCTT...
NM_199355.3:c.496-28625_496-28607delinsCCATATTGATAAATTTCTT	NP_955387.1:n.496-28625_496-28607delinsCCATATTGATAAATTTCTT
XM_011522924.2:c.-25-28625_-25-28607delinsCCATATTGATAAATTTCTT	XP_011521226.1:n.-25-28625_-25-28607delinsCCATATTGATAAATTTCTT...
XM_017022988.2:c.-585-28625_-585-28607delinsCCATATTGATAAATTTCTT	XP_016878477.1:n.-585-28625_-585-28607delinsCCATATTGATAAATTTC...
XM_017022989.1:c.-581-28625_-581-28607delinsCCATATTGATAAATTTCTT	XP_016878478.1:n.-581-28625_-581-28607delinsCCATATTGATAAATTTC...
NM_199355.4:c.496-28625_496-28607delinsCCATATTGATAAATTTCTT MANE Select	NP_955387.1:n.496-28625_496-28607delinsCCATATTGATAAATTTCTT
NM_001326358.2:c.-25-28625_-25-28607delinsCCATATTGATAAATTTCTT	NP_001313287.1:n.-25-28625_-25-28607delinsCCATATTGATAAATTTCTT...