Canonical Allele Identifier: CA496590784

Gene: ADAMTS18

Linked Data

• MyVariant Identifiers: chr16:g.77369793C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77335896C>G , CM000678.2:g.77335896C>G	GRCh38
NC_000016.9:g.77369793C>G , CM000678.1:g.77369793C>G	GRCh37
NC_000016.8:g.75927294C>G	NCBI36
NG_031879.1:g.104219G>C
NG_031879.2:g.104219G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.1719G>C MANE Select	ENSP00000282849.5:p.Arg573=
ENST00000282849.9:c.1719G>C	ENSP00000282849.5:p.Arg573=
NM_199355.2:c.1719G>C	NP_955387.1:p.Arg573=
XM_011522923.1:c.1203G>C	XP_011521225.1:p.Arg401=
XM_011522924.1:c.1203G>C	XP_011521226.1:p.Arg401=
NM_001326358.1:c.1203G>C	NP_001313287.1:p.Arg401=
NM_199355.3:c.1719G>C	NP_955387.1:p.Arg573=
XM_011522924.2:c.1203G>C	XP_011521226.1:p.Arg401=
XM_017022988.2:c.483G>C	XP_016878477.1:p.Arg161=
XM_017022989.1:c.483G>C	XP_016878478.1:p.Arg161=
NM_199355.4:c.1719G>C MANE Select	NP_955387.1:p.Arg573=
NM_001326358.2:c.1203G>C	NP_001313287.1:p.Arg401=