Canonical Allele Identifier: CA284427571
Gene: ADAMTS18 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.77295744T>G , CM000678.2:g.77295744T>G GRCh38
NC_000016.9:g.77329641T>G , CM000678.1:g.77329641T>G GRCh37
NC_000016.8:g.75887142T>G NCBI36
NG_031879.1:g.144371A>C
NG_031879.2:g.144371A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282849.10:c.2802-617A>C MANE Select ENSP00000282849.5:n.2802-617A>C
ENST00000282849.9:c.2802-617A>C ENSP00000282849.5:n.2802-617A>C
NM_199355.2:c.2802-617A>C NP_955387.1:n.2802-617A>C
XM_006721158.2:c.714-617A>C XP_006721221.1:n.714-617A>C
XM_011522923.1:c.2286-617A>C XP_011521225.1:n.2286-617A>C
XM_011522924.1:c.2286-617A>C XP_011521226.1:n.2286-617A>C
NM_001326358.1:c.2286-617A>C NP_001313287.1:n.2286-617A>C
NM_199355.3:c.2802-617A>C NP_955387.1:n.2802-617A>C
XM_011522924.2:c.2286-617A>C XP_011521226.1:n.2286-617A>C
XM_017022988.2:c.1566-617A>C XP_016878477.1:n.1566-617A>C
XM_017022989.1:c.1566-617A>C XP_016878478.1:n.1566-617A>C
NM_199355.4:c.2802-617A>C MANE Select NP_955387.1:n.2802-617A>C
NM_001326358.2:c.2286-617A>C NP_001313287.1:n.2286-617A>C
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