Canonical Allele Identifier: CA2234426734
Gene: ADAMTS18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77294919T= , CM000678.2:g.77294919T= GRCh38
NC_000016.9:g.77328816T= , CM000678.1:g.77328816T= GRCh37
NC_000016.8:g.75886317T= NCBI36
NG_031879.1:g.145196A=
NG_031879.2:g.145196A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282849.10:c.3006+4A= MANE Select ENSP00000282849.5:n.3006+4A=
ENST00000282849.9:c.3006+4A= ENSP00000282849.5:n.3006+4A=
NM_199355.2:c.3006+4A= NP_955387.1:n.3006+4A=
XM_006721158.2:c.918+4A= XP_006721221.1:n.918+4A=
XM_011522923.1:c.2490+4A= XP_011521225.1:n.2490+4A=
XM_011522924.1:c.2490+4A= XP_011521226.1:n.2490+4A=
NM_001326358.1:c.2490+4A= NP_001313287.1:n.2490+4A=
NM_199355.3:c.3006+4A= NP_955387.1:n.3006+4A=
XM_011522924.2:c.2490+4A= XP_011521226.1:n.2490+4A=
XM_017022988.2:c.1770+4A= XP_016878477.1:n.1770+4A=
XM_017022989.1:c.1770+4A= XP_016878478.1:n.1770+4A=
NM_199355.4:c.3006+4A= MANE Select NP_955387.1:n.3006+4A=
NM_001326358.2:c.2490+4A= NP_001313287.1:n.2490+4A=