Canonical Allele Identifier: CA2234406037
Gene: ADAMTS18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77335785C= , CM000678.2:g.77335785C= GRCh38
NC_000016.9:g.77369682C= , CM000678.1:g.77369682C= GRCh37
NC_000016.8:g.75927183C= NCBI36
NG_031879.1:g.104330G=
NG_031879.2:g.104330G=

Transcript Alleles

HGVS Amino-acid change
ENST00000282849.10:c.1830G= MANE Select ENSP00000282849.5:p.Lys610=
ENST00000282849.9:c.1830G= ENSP00000282849.5:p.Lys610=
NM_199355.2:c.1830G= NP_955387.1:p.Lys610=
XM_006721158.2:c.-86G= XP_006721221.1:n.-86G=
XM_011522923.1:c.1314G= XP_011521225.1:p.Lys438=
XM_011522924.1:c.1314G= XP_011521226.1:p.Lys438=
NM_001326358.1:c.1314G= NP_001313287.1:p.Lys438=
NM_199355.3:c.1830G= NP_955387.1:p.Lys610=
XM_011522924.2:c.1314G= XP_011521226.1:p.Lys438=
XM_017022988.2:c.594G= XP_016878477.1:p.Lys198=
XM_017022989.1:c.594G= XP_016878478.1:p.Lys198=
NM_199355.4:c.1830G= MANE Select NP_955387.1:p.Lys610=
NM_001326358.2:c.1314G= NP_001313287.1:p.Lys438=