Canonical Allele Identifier: CA2234406218
Gene: ADAMTS18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77335884G= , CM000678.2:g.77335884G= GRCh38
NC_000016.9:g.77369781G= , CM000678.1:g.77369781G= GRCh37
NC_000016.8:g.75927282G= NCBI36
NG_031879.1:g.104231C=
NG_031879.2:g.104231C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282849.10:c.1731C= MANE Select ENSP00000282849.5:p.Cys577=
ENST00000282849.9:c.1731C= ENSP00000282849.5:p.Cys577=
NM_199355.2:c.1731C= NP_955387.1:p.Cys577=
XM_011522923.1:c.1215C= XP_011521225.1:p.Cys405=
XM_011522924.1:c.1215C= XP_011521226.1:p.Cys405=
NM_001326358.1:c.1215C= NP_001313287.1:p.Cys405=
NM_199355.3:c.1731C= NP_955387.1:p.Cys577=
XM_011522924.2:c.1215C= XP_011521226.1:p.Cys405=
XM_017022988.2:c.495C= XP_016878477.1:p.Cys165=
XM_017022989.1:c.495C= XP_016878478.1:p.Cys165=
NM_199355.4:c.1731C= MANE Select NP_955387.1:p.Cys577=
NM_001326358.2:c.1215C= NP_001313287.1:p.Cys405=