Canonical Allele Identifier: CA396831896

Gene: ADAMTS18

Linked Data

• MyVariant Identifiers: chr16:g.77369689C>T (hg19) ; chr16:g.77335792C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77335792C>T , CM000678.2:g.77335792C>T	GRCh38
NC_000016.9:g.77369689C>T , CM000678.1:g.77369689C>T	GRCh37
NC_000016.8:g.75927190C>T	NCBI36
NG_031879.1:g.104323G>A
NG_031879.2:g.104323G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.1823G>A MANE Select	ENSP00000282849.5:p.Gly608Glu
ENST00000282849.9:c.1823G>A	ENSP00000282849.5:p.Gly608Glu
NM_199355.2:c.1823G>A	NP_955387.1:p.Gly608Glu
XM_006721158.2:c.-93G>A	XP_006721221.1:n.-93G>A
XM_011522923.1:c.1307G>A	XP_011521225.1:p.Gly436Glu
XM_011522924.1:c.1307G>A	XP_011521226.1:p.Gly436Glu
NM_001326358.1:c.1307G>A	NP_001313287.1:p.Gly436Glu
NM_199355.3:c.1823G>A	NP_955387.1:p.Gly608Glu
XM_011522924.2:c.1307G>A	XP_011521226.1:p.Gly436Glu
XM_017022988.2:c.587G>A	XP_016878477.1:p.Gly196Glu
XM_017022989.1:c.587G>A	XP_016878478.1:p.Gly196Glu
NM_199355.4:c.1823G>A MANE Select	NP_955387.1:p.Gly608Glu
NM_001326358.2:c.1307G>A	NP_001313287.1:p.Gly436Glu