Canonical Allele Identifier: CA2234466572
Gene: ADAMTS18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77395079T= , CM000678.2:g.77395079T= GRCh38
NC_000016.9:g.77428976T= , CM000678.1:g.77428976T= GRCh37
NC_000016.8:g.75986477T= NCBI36
NG_031879.1:g.45036A=
NG_031879.2:g.45036A=

Transcript Alleles

HGVS Amino-acid change
ENST00000282849.10:c.496-27356A= MANE Select ENSP00000282849.5:n.496-27356A=
ENST00000282849.9:c.496-27356A= ENSP00000282849.5:n.496-27356A=
ENST00000449265.2:c.496-27356A= ENSP00000392540.2:n.496-27356A=
ENST00000562345.1:c.294-27410A=
ENST00000564369.1:n.422-27356A=
ENST00000567121.5:n.353-27356A=
ENST00000567914.1:n.340-27356A=
ENST00000569309.1:n.453-16100A=
NM_199355.2:c.496-27356A= NP_955387.1:n.496-27356A=
XM_011522923.1:c.-25-27356A= XP_011521225.1:n.-25-27356A=
XM_011522924.1:c.-25-27356A= XP_011521226.1:n.-25-27356A=
NM_001326358.1:c.-25-27356A= NP_001313287.1:n.-25-27356A=
NM_199355.3:c.496-27356A= NP_955387.1:n.496-27356A=
XM_011522924.2:c.-25-27356A= XP_011521226.1:n.-25-27356A=
XM_017022988.2:c.-585-27356A= XP_016878477.1:n.-585-27356A=
XM_017022989.1:c.-581-27356A= XP_016878478.1:n.-581-27356A=
NM_199355.4:c.496-27356A= MANE Select NP_955387.1:n.496-27356A=
NM_001326358.2:c.-25-27356A= NP_001313287.1:n.-25-27356A=