Canonical Allele Identifier: CA2234406242
Gene: ADAMTS18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77335890G= , CM000678.2:g.77335890G= GRCh38
NC_000016.9:g.77369787G= , CM000678.1:g.77369787G= GRCh37
NC_000016.8:g.75927288G= NCBI36
NG_031879.1:g.104225C=
NG_031879.2:g.104225C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282849.10:c.1725C= MANE Select ENSP00000282849.5:p.Gly575=
ENST00000282849.9:c.1725C= ENSP00000282849.5:p.Gly575=
NM_199355.2:c.1725C= NP_955387.1:p.Gly575=
XM_011522923.1:c.1209C= XP_011521225.1:p.Gly403=
XM_011522924.1:c.1209C= XP_011521226.1:p.Gly403=
NM_001326358.1:c.1209C= NP_001313287.1:p.Gly403=
NM_199355.3:c.1725C= NP_955387.1:p.Gly575=
XM_011522924.2:c.1209C= XP_011521226.1:p.Gly403=
XM_017022988.2:c.489C= XP_016878477.1:p.Gly163=
XM_017022989.1:c.489C= XP_016878478.1:p.Gly163=
NM_199355.4:c.1725C= MANE Select NP_955387.1:p.Gly575=
NM_001326358.2:c.1209C= NP_001313287.1:p.Gly403=