Canonical Allele Identifier: CA724135107

Gene: ADAMTS18

Linked Data

• dbSNP Id: rs1485139920
• MyVariant Identifiers: chr16:g.77429012_77429013insC (hg19) ; chr16:g.77395115_77395116insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77395117dup , CM000678.2:g.77395117dup	GRCh38
NC_000016.9:g.77429014dup , CM000678.1:g.77429014dup	GRCh37
NC_000016.8:g.75986515dup	NCBI36
NG_031879.1:g.44999dup
NG_031879.2:g.44999dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000282849.10:c.496-27393dup MANE Select	ENSP00000282849.5:n.496-27393dup
ENST00000282849.9:c.496-27393dup	ENSP00000282849.5:n.496-27393dup
ENST00000449265.2:c.496-27393dup	ENSP00000392540.2:n.496-27393dup
ENST00000562345.1:c.294-27447dup
ENST00000564369.1:n.422-27393dup
ENST00000567121.5:n.353-27393dup
ENST00000567914.1:n.340-27393dup
ENST00000569309.1:n.453-16137dup
NM_199355.2:c.496-27393dup	NP_955387.1:n.496-27393dup
XM_011522923.1:c.-25-27393dup	XP_011521225.1:n.-25-27393dup
XM_011522924.1:c.-25-27393dup	XP_011521226.1:n.-25-27393dup
NM_001326358.1:c.-25-27393dup	NP_001313287.1:n.-25-27393dup
NM_199355.3:c.496-27393dup	NP_955387.1:n.496-27393dup
XM_011522924.2:c.-25-27393dup	XP_011521226.1:n.-25-27393dup
XM_017022988.2:c.-585-27393dup	XP_016878477.1:n.-585-27393dup
XM_017022989.1:c.-581-27393dup	XP_016878478.1:n.-581-27393dup
NM_199355.4:c.496-27393dup MANE Select	NP_955387.1:n.496-27393dup
NM_001326358.2:c.-25-27393dup	NP_001313287.1:n.-25-27393dup