Canonical Allele Identifier: CA2807716820

Gene: ADAMTS18

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77335799_77335801del , CM000678.2:g.77335799_77335801del	GRCh38
NC_000016.9:g.77369696_77369698del , CM000678.1:g.77369696_77369698del	GRCh37
NC_000016.8:g.75927197_75927199del	NCBI36
NG_031879.1:g.104318_104320del
NG_031879.2:g.104318_104320del

Transcript Alleles

HGVS	Amino-acid change
ENST00000282849.10:c.1818_1820del MANE Select	ENSP00000282849.5:p.Gly607del
ENST00000282849.9:c.1818_1820del	ENSP00000282849.5:p.Gly607del
NM_199355.2:c.1818_1820del	NP_955387.1:p.Gly607del
XM_006721158.2:c.-98_-96del	XP_006721221.1:n.-98_-96del
XM_011522923.1:c.1302_1304del	XP_011521225.1:p.Gly435del
XM_011522924.1:c.1302_1304del	XP_011521226.1:p.Gly435del
NM_001326358.1:c.1302_1304del	NP_001313287.1:p.Gly435del
NM_199355.3:c.1818_1820del	NP_955387.1:p.Gly607del
XM_011522924.2:c.1302_1304del	XP_011521226.1:p.Gly435del
XM_017022988.2:c.582_584del	XP_016878477.1:p.Gly195del
XM_017022989.1:c.582_584del	XP_016878478.1:p.Gly195del
NM_199355.4:c.1818_1820del MANE Select	NP_955387.1:p.Gly607del
NM_001326358.2:c.1302_1304del	NP_001313287.1:p.Gly435del