Canonical Allele Identifier: CA396831892

Gene: ADAMTS18

Linked Data

• MyVariant Identifiers: chr16:g.77369687C>T (hg19) ; chr16:g.77335790C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77335790C>T , CM000678.2:g.77335790C>T	GRCh38
NC_000016.9:g.77369687C>T , CM000678.1:g.77369687C>T	GRCh37
NC_000016.8:g.75927188C>T	NCBI36
NG_031879.1:g.104325G>A
NG_031879.2:g.104325G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.1825G>A MANE Select	ENSP00000282849.5:p.Val609Ile
ENST00000282849.9:c.1825G>A	ENSP00000282849.5:p.Val609Ile
NM_199355.2:c.1825G>A	NP_955387.1:p.Val609Ile
XM_006721158.2:c.-91G>A	XP_006721221.1:n.-91G>A
XM_011522923.1:c.1309G>A	XP_011521225.1:p.Val437Ile
XM_011522924.1:c.1309G>A	XP_011521226.1:p.Val437Ile
NM_001326358.1:c.1309G>A	NP_001313287.1:p.Val437Ile
NM_199355.3:c.1825G>A	NP_955387.1:p.Val609Ile
XM_011522924.2:c.1309G>A	XP_011521226.1:p.Val437Ile
XM_017022988.2:c.589G>A	XP_016878477.1:p.Val197Ile
XM_017022989.1:c.589G>A	XP_016878478.1:p.Val197Ile
NM_199355.4:c.1825G>A MANE Select	NP_955387.1:p.Val609Ile
NM_001326358.2:c.1309G>A	NP_001313287.1:p.Val437Ile