Canonical Allele Identifier: CA2234465275

Gene: ADAMTS18

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77393886_77393887delinsCA , CM000678.2:g.77393886_77393887delinsCA	GRCh38
NC_000016.9:g.77427783_77427784delinsCA , CM000678.1:g.77427783_77427784delinsCA	GRCh37
NC_000016.8:g.75985284_75985285delinsCA	NCBI36
NG_031879.1:g.46228_46229delinsTG
NG_031879.2:g.46228_46229delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.496-26164_496-26163delinsTG MANE Select	ENSP00000282849.5:n.496-26164_496-26163delinsTG
ENST00000282849.9:c.496-26164_496-26163delinsTG	ENSP00000282849.5:n.496-26164_496-26163delinsTG
ENST00000449265.2:c.496-26164_496-26163delinsTG	ENSP00000392540.2:n.496-26164_496-26163delinsTG
ENST00000562345.1:c.294-26218_294-26217delinsTG
ENST00000564369.1:n.422-26164_422-26163delinsTG
ENST00000567121.5:n.353-26164_353-26163delinsTG
ENST00000567914.1:n.340-26164_340-26163delinsTG
ENST00000569309.1:n.453-14908_453-14907delinsTG
NM_199355.2:c.496-26164_496-26163delinsTG	NP_955387.1:n.496-26164_496-26163delinsTG
XM_011522923.1:c.-25-26164_-25-26163delinsTG	XP_011521225.1:n.-25-26164_-25-26163delinsTG
XM_011522924.1:c.-25-26164_-25-26163delinsTG	XP_011521226.1:n.-25-26164_-25-26163delinsTG
NM_001326358.1:c.-25-26164_-25-26163delinsTG	NP_001313287.1:n.-25-26164_-25-26163delinsTG
NM_199355.3:c.496-26164_496-26163delinsTG	NP_955387.1:n.496-26164_496-26163delinsTG
XM_011522924.2:c.-25-26164_-25-26163delinsTG	XP_011521226.1:n.-25-26164_-25-26163delinsTG
XM_017022988.2:c.-585-26164_-585-26163delinsTG	XP_016878477.1:n.-585-26164_-585-26163delinsTG
XM_017022989.1:c.-581-26164_-581-26163delinsTG	XP_016878478.1:n.-581-26164_-581-26163delinsTG
NM_199355.4:c.496-26164_496-26163delinsTG MANE Select	NP_955387.1:n.496-26164_496-26163delinsTG
NM_001326358.2:c.-25-26164_-25-26163delinsTG	NP_001313287.1:n.-25-26164_-25-26163delinsTG