Canonical Allele Identifier: CA2234468212

Gene: ADAMTS18

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77396391_77396392delinsCA , CM000678.2:g.77396391_77396392delinsCA	GRCh38
NC_000016.9:g.77430288_77430289delinsCA , CM000678.1:g.77430288_77430289delinsCA	GRCh37
NC_000016.8:g.75987789_75987790delinsCA	NCBI36
NG_031879.1:g.43723_43724delinsTG
NG_031879.2:g.43723_43724delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.496-28669_496-28668delinsTG MANE Select	ENSP00000282849.5:n.496-28669_496-28668delinsTG
ENST00000282849.9:c.496-28669_496-28668delinsTG	ENSP00000282849.5:n.496-28669_496-28668delinsTG
ENST00000449265.2:c.496-28669_496-28668delinsTG	ENSP00000392540.2:n.496-28669_496-28668delinsTG
ENST00000562345.1:c.294-28723_294-28722delinsTG
ENST00000564369.1:n.422-28669_422-28668delinsTG
ENST00000567121.5:n.353-28669_353-28668delinsTG
ENST00000567914.1:n.340-28669_340-28668delinsTG
ENST00000569309.1:n.453-17413_453-17412delinsTG
NM_199355.2:c.496-28669_496-28668delinsTG	NP_955387.1:n.496-28669_496-28668delinsTG
XM_011522923.1:c.-25-28669_-25-28668delinsTG	XP_011521225.1:n.-25-28669_-25-28668delinsTG
XM_011522924.1:c.-25-28669_-25-28668delinsTG	XP_011521226.1:n.-25-28669_-25-28668delinsTG
NM_001326358.1:c.-25-28669_-25-28668delinsTG	NP_001313287.1:n.-25-28669_-25-28668delinsTG
NM_199355.3:c.496-28669_496-28668delinsTG	NP_955387.1:n.496-28669_496-28668delinsTG
XM_011522924.2:c.-25-28669_-25-28668delinsTG	XP_011521226.1:n.-25-28669_-25-28668delinsTG
XM_017022988.2:c.-585-28669_-585-28668delinsTG	XP_016878477.1:n.-585-28669_-585-28668delinsTG
XM_017022989.1:c.-581-28669_-581-28668delinsTG	XP_016878478.1:n.-581-28669_-581-28668delinsTG
NM_199355.4:c.496-28669_496-28668delinsTG MANE Select	NP_955387.1:n.496-28669_496-28668delinsTG
NM_001326358.2:c.-25-28669_-25-28668delinsTG	NP_001313287.1:n.-25-28669_-25-28668delinsTG