Canonical Allele Identifier: CA2234406046
Gene: ADAMTS18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77335791T= , CM000678.2:g.77335791T= GRCh38
NC_000016.9:g.77369688T= , CM000678.1:g.77369688T= GRCh37
NC_000016.8:g.75927189T= NCBI36
NG_031879.1:g.104324A=
NG_031879.2:g.104324A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282849.10:c.1824A= MANE Select ENSP00000282849.5:p.Gly608=
ENST00000282849.9:c.1824A= ENSP00000282849.5:p.Gly608=
NM_199355.2:c.1824A= NP_955387.1:p.Gly608=
XM_006721158.2:c.-92A= XP_006721221.1:n.-92A=
XM_011522923.1:c.1308A= XP_011521225.1:p.Gly436=
XM_011522924.1:c.1308A= XP_011521226.1:p.Gly436=
NM_001326358.1:c.1308A= NP_001313287.1:p.Gly436=
NM_199355.3:c.1824A= NP_955387.1:p.Gly608=
XM_011522924.2:c.1308A= XP_011521226.1:p.Gly436=
XM_017022988.2:c.588A= XP_016878477.1:p.Gly196=
XM_017022989.1:c.588A= XP_016878478.1:p.Gly196=
NM_199355.4:c.1824A= MANE Select NP_955387.1:p.Gly608=
NM_001326358.2:c.1308A= NP_001313287.1:p.Gly436=