Canonical Allele Identifier: CA979259298

Gene: ADAMTS18

Linked Data

• dbSNP Id: rs2057222408

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77393840A>G , CM000678.2:g.77393840A>G	GRCh38
NC_000016.9:g.77427737A>G , CM000678.1:g.77427737A>G	GRCh37
NC_000016.8:g.75985238A>G	NCBI36
NG_031879.1:g.46275T>C
NG_031879.2:g.46275T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.496-26117T>C MANE Select	ENSP00000282849.5:n.496-26117T>C
ENST00000282849.9:c.496-26117T>C	ENSP00000282849.5:n.496-26117T>C
ENST00000449265.2:c.496-26117T>C	ENSP00000392540.2:n.496-26117T>C
ENST00000562345.1:c.294-26171T>C
ENST00000564369.1:n.422-26117T>C
ENST00000567121.5:n.353-26117T>C
ENST00000567914.1:n.340-26117T>C
ENST00000569309.1:n.453-14861T>C
NM_199355.2:c.496-26117T>C	NP_955387.1:n.496-26117T>C
XM_011522923.1:c.-25-26117T>C	XP_011521225.1:n.-25-26117T>C
XM_011522924.1:c.-25-26117T>C	XP_011521226.1:n.-25-26117T>C
NM_001326358.1:c.-25-26117T>C	NP_001313287.1:n.-25-26117T>C
NM_199355.3:c.496-26117T>C	NP_955387.1:n.496-26117T>C
XM_011522924.2:c.-25-26117T>C	XP_011521226.1:n.-25-26117T>C
XM_017022988.2:c.-585-26117T>C	XP_016878477.1:n.-585-26117T>C
XM_017022989.1:c.-581-26117T>C	XP_016878478.1:n.-581-26117T>C
NM_199355.4:c.496-26117T>C MANE Select	NP_955387.1:n.496-26117T>C
NM_001326358.2:c.-25-26117T>C	NP_001313287.1:n.-25-26117T>C