Canonical Allele Identifier: CA724134184

Gene: ADAMTS18

Linked Data

• dbSNP Id: rs1206485115
• gnomAD v3: 16-77393623-CAAG-C
• gnomAD v4: 16-77393623-CAAG-C
• MyVariant Identifiers: chr16:g.77427521_77427523del (hg19) ; chr16:g.77393624_77393626del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77393627_77393629del , CM000678.2:g.77393627_77393629del	GRCh38
NC_000016.9:g.77427524_77427526del , CM000678.1:g.77427524_77427526del	GRCh37
NC_000016.8:g.75985025_75985027del	NCBI36
NG_031879.1:g.46489_46491del
NG_031879.2:g.46489_46491del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.496-25903_496-25901del MANE Select	ENSP00000282849.5:n.496-25903_496-25901del
ENST00000282849.9:c.496-25903_496-25901del	ENSP00000282849.5:n.496-25903_496-25901del
ENST00000449265.2:c.496-25903_496-25901del	ENSP00000392540.2:n.496-25903_496-25901del
ENST00000562345.1:c.294-25957_294-25955del
ENST00000564369.1:n.422-25903_422-25901del
ENST00000567121.5:n.353-25903_353-25901del
ENST00000567914.1:n.340-25903_340-25901del
ENST00000569309.1:n.453-14647_453-14645del
NM_199355.2:c.496-25903_496-25901del	NP_955387.1:n.496-25903_496-25901del
XM_011522923.1:c.-25-25903_-25-25901del	XP_011521225.1:n.-25-25903_-25-25901del
XM_011522924.1:c.-25-25903_-25-25901del	XP_011521226.1:n.-25-25903_-25-25901del
NM_001326358.1:c.-25-25903_-25-25901del	NP_001313287.1:n.-25-25903_-25-25901del
NM_199355.3:c.496-25903_496-25901del	NP_955387.1:n.496-25903_496-25901del
XM_011522924.2:c.-25-25903_-25-25901del	XP_011521226.1:n.-25-25903_-25-25901del
XM_017022988.2:c.-585-25903_-585-25901del	XP_016878477.1:n.-585-25903_-585-25901del
XM_017022989.1:c.-581-25903_-581-25901del	XP_016878478.1:n.-581-25903_-581-25901del
NM_199355.4:c.496-25903_496-25901del MANE Select	NP_955387.1:n.496-25903_496-25901del
NM_001326358.2:c.-25-25903_-25-25901del	NP_001313287.1:n.-25-25903_-25-25901del