Canonical Allele Identifier: CA396833278

Gene: ADAMTS18

Linked Data

• MyVariant Identifiers: chr16:g.77328818A>T (hg19) ; chr16:g.77294921A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77294921A>T , CM000678.2:g.77294921A>T	GRCh38
NC_000016.9:g.77328818A>T , CM000678.1:g.77328818A>T	GRCh37
NC_000016.8:g.75886319A>T	NCBI36
NG_031879.1:g.145194T>A
NG_031879.2:g.145194T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000282849.10:c.3006+2T>A MANE Select	ENSP00000282849.5:n.3006+2T>A
ENST00000282849.9:c.3006+2T>A	ENSP00000282849.5:n.3006+2T>A
NM_199355.2:c.3006+2T>A	NP_955387.1:n.3006+2T>A
XM_006721158.2:c.918+2T>A	XP_006721221.1:n.918+2T>A
XM_011522923.1:c.2490+2T>A	XP_011521225.1:n.2490+2T>A
XM_011522924.1:c.2490+2T>A	XP_011521226.1:n.2490+2T>A
NM_001326358.1:c.2490+2T>A	NP_001313287.1:n.2490+2T>A
NM_199355.3:c.3006+2T>A	NP_955387.1:n.3006+2T>A
XM_011522924.2:c.2490+2T>A	XP_011521226.1:n.2490+2T>A
XM_017022988.2:c.1770+2T>A	XP_016878477.1:n.1770+2T>A
XM_017022989.1:c.1770+2T>A	XP_016878478.1:n.1770+2T>A
NM_199355.4:c.3006+2T>A MANE Select	NP_955387.1:n.3006+2T>A
NM_001326358.2:c.2490+2T>A	NP_001313287.1:n.2490+2T>A