Canonical Allele Identifier: CA8180421

Gene: ADAMTS18

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77289350C>T , CM000678.2:g.77289350C>T	GRCh38
NC_000016.9:g.77323247C>T , CM000678.1:g.77323247C>T	GRCh37
NC_000016.8:g.75880748C>T	NCBI36
NG_031879.1:g.150765G>A
NG_031879.2:g.150765G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.3464G>A MANE Select	ENSP00000282849.5:p.Arg1155Gln
ENST00000282849.9:c.3464G>A	ENSP00000282849.5:p.Arg1155Gln
ENST00000562332.1:c.10G>A
NM_199355.2:c.3464G>A	NP_955387.1:p.Arg1155Gln
XM_006721158.2:c.1376G>A	XP_006721221.1:p.Arg459Gln
XM_011522923.1:c.2948G>A	XP_011521225.1:p.Arg983Gln
XM_011522924.1:c.2735G>A	XP_011521226.1:p.Arg912Gln
NM_001326358.1:c.2948G>A	NP_001313287.1:p.Arg983Gln
NM_199355.3:c.3464G>A	NP_955387.1:p.Arg1155Gln
XM_011522924.2:c.2735G>A	XP_011521226.1:p.Arg912Gln
XM_017022988.2:c.2228G>A	XP_016878477.1:p.Arg743Gln
XM_017022989.1:c.2228G>A	XP_016878478.1:p.Arg743Gln
NM_199355.4:c.3464G>A MANE Select	NP_955387.1:p.Arg1155Gln
NM_001326358.2:c.2948G>A	NP_001313287.1:p.Arg983Gln