Canonical Allele Identifier: CA284410248

Gene: ADAMTS18

Linked Data

• dbSNP Id: rs927331733
• gnomAD v2: 16-77427565-C-A
• gnomAD v3: 16-77393668-C-A
• gnomAD v4: 16-77393668-C-A
• MyVariant Identifiers: chr16:g.77427565C>A (hg19) ; chr16:g.77393668C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77393668C>A , CM000678.2:g.77393668C>A	GRCh38
NC_000016.9:g.77427565C>A , CM000678.1:g.77427565C>A	GRCh37
NC_000016.8:g.75985066C>A	NCBI36
NG_031879.1:g.46447G>T
NG_031879.2:g.46447G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.496-25945G>T MANE Select	ENSP00000282849.5:n.496-25945G>T
ENST00000282849.9:c.496-25945G>T	ENSP00000282849.5:n.496-25945G>T
ENST00000449265.2:c.496-25945G>T	ENSP00000392540.2:n.496-25945G>T
ENST00000562345.1:c.294-25999G>T
ENST00000564369.1:n.422-25945G>T
ENST00000567121.5:n.353-25945G>T
ENST00000567914.1:n.340-25945G>T
ENST00000569309.1:n.453-14689G>T
NM_199355.2:c.496-25945G>T	NP_955387.1:n.496-25945G>T
XM_011522923.1:c.-25-25945G>T	XP_011521225.1:n.-25-25945G>T
XM_011522924.1:c.-25-25945G>T	XP_011521226.1:n.-25-25945G>T
NM_001326358.1:c.-25-25945G>T	NP_001313287.1:n.-25-25945G>T
NM_199355.3:c.496-25945G>T	NP_955387.1:n.496-25945G>T
XM_011522924.2:c.-25-25945G>T	XP_011521226.1:n.-25-25945G>T
XM_017022988.2:c.-585-25945G>T	XP_016878477.1:n.-585-25945G>T
XM_017022989.1:c.-581-25945G>T	XP_016878478.1:n.-581-25945G>T
NM_199355.4:c.496-25945G>T MANE Select	NP_955387.1:n.496-25945G>T
NM_001326358.2:c.-25-25945G>T	NP_001313287.1:n.-25-25945G>T