Canonical Allele Identifier: CA2234426737

Gene: ADAMTS18

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77294924T= , CM000678.2:g.77294924T=	GRCh38
NC_000016.9:g.77328821T= , CM000678.1:g.77328821T=	GRCh37
NC_000016.8:g.75886322T=	NCBI36
NG_031879.1:g.145191A=
NG_031879.2:g.145191A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000282849.10:c.3005A= MANE Select	ENSP00000282849.5:p.Gln1002=
ENST00000282849.9:c.3005A=	ENSP00000282849.5:p.Gln1002=
NM_199355.2:c.3005A=	NP_955387.1:p.Gln1002=
XM_006721158.2:c.917A=	XP_006721221.1:p.Gln306=
XM_011522923.1:c.2489A=	XP_011521225.1:p.Gln830=
XM_011522924.1:c.2489A=	XP_011521226.1:p.Gln830=
NM_001326358.1:c.2489A=	NP_001313287.1:p.Gln830=
NM_199355.3:c.3005A=	NP_955387.1:p.Gln1002=
XM_011522924.2:c.2489A=	XP_011521226.1:p.Gln830=
XM_017022988.2:c.1769A=	XP_016878477.1:p.Gln590=
XM_017022989.1:c.1769A=	XP_016878478.1:p.Gln590=
NM_199355.4:c.3005A= MANE Select	NP_955387.1:p.Gln1002=
NM_001326358.2:c.2489A=	NP_001313287.1:p.Gln830=