Canonical Allele Identifier: CA2234406049
Gene: ADAMTS18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77335792C= , CM000678.2:g.77335792C= GRCh38
NC_000016.9:g.77369689C= , CM000678.1:g.77369689C= GRCh37
NC_000016.8:g.75927190C= NCBI36
NG_031879.1:g.104323G=
NG_031879.2:g.104323G=

Transcript Alleles

HGVS Amino-acid change
ENST00000282849.10:c.1823G= MANE Select ENSP00000282849.5:p.Gly608=
ENST00000282849.9:c.1823G= ENSP00000282849.5:p.Gly608=
NM_199355.2:c.1823G= NP_955387.1:p.Gly608=
XM_006721158.2:c.-93G= XP_006721221.1:n.-93G=
XM_011522923.1:c.1307G= XP_011521225.1:p.Gly436=
XM_011522924.1:c.1307G= XP_011521226.1:p.Gly436=
NM_001326358.1:c.1307G= NP_001313287.1:p.Gly436=
NM_199355.3:c.1823G= NP_955387.1:p.Gly608=
XM_011522924.2:c.1307G= XP_011521226.1:p.Gly436=
XM_017022988.2:c.587G= XP_016878477.1:p.Gly196=
XM_017022989.1:c.587G= XP_016878478.1:p.Gly196=
NM_199355.4:c.1823G= MANE Select NP_955387.1:p.Gly608=
NM_001326358.2:c.1307G= NP_001313287.1:p.Gly436=