Canonical Allele Identifier: CA2573130176

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29674886del , CM000684.2:g.29674886del	GRCh38
NC_000022.10:g.30070875del , CM000684.1:g.30070875del	GRCh37
NC_000022.9:g.28400875del	NCBI36
NG_009057.1:g.76331del , LRG_511:g.76331del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1256del	ENSP00000354529.6:p.Ala419GlyfsTer21
ENST00000673312.2:c.*885del	ENSP00000500186.2:n.*885del
ENST00000338641.10:c.1391del MANE Select	ENSP00000344666.5:p.Ala464GlyfsTer21
ENST00000361166.9:c.809del	ENSP00000354529.5:p.Ala270GlyfsTer21
ENST00000672461.1:c.1391del	ENSP00000500919.1:p.Ala464GlyfsTer21
ENST00000672805.1:c.*1273del	ENSP00000500295.1:n.*1273del
ENST00000672896.1:c.1391del	ENSP00000500117.1:p.Ala464GlyfsTer21
ENST00000673312.1:c.1410del	ENSP00000500186.1:n.1410del
ENST00000334961.11:c.1142del	ENSP00000335652.7:p.Ala381GlyfsTer21
ENST00000338641.8:c.1391del	ENSP00000344666.4:p.Ala464GlyfsTer21
ENST00000353887.8:c.1142del	ENSP00000340626.4:p.Ala381GlyfsTer21
ENST00000361166.8:c.1391del	ENSP00000354529.4:p.Ala464GlyfsTer21
ENST00000361452.8:c.1268del	ENSP00000354897.4:p.Ala423GlyfsTer21
ENST00000361676.8:c.1265del	ENSP00000355183.4:p.Ala422GlyfsTer21
ENST00000397789.3:c.1391del	ENSP00000380891.3:p.Ala464GlyfsTer21
ENST00000403435.5:c.1304del	ENSP00000384029.1:p.Ala435GlyfsTer21
ENST00000403999.7:c.1391del	ENSP00000384797.3:p.Ala464GlyfsTer21
ENST00000413209.6:c.448-19866del	ENSP00000409921.2:n.448-19866del
ENST00000432151.5:c.573del	ENSP00000395885.1:p.Gly192GlufsTer?
NM_000268.3:c.1391del , LRG_511t1:c.1391del	NP_000259.1:p.Ala464GlyfsTer21
NM_016418.5:c.1391del , LRG_511t2:c.1391del	NP_057502.2:p.Ala464GlyfsTer21
NM_181825.2:c.1391del	NP_861546.1:p.Ala464GlyfsTer21
NM_181828.2:c.1265del	NP_861966.1:p.Ala422GlyfsTer21
NM_181829.2:c.1268del	NP_861967.1:p.Ala423GlyfsTer21
NM_181830.2:c.1142del	NP_861968.1:p.Ala381GlyfsTer21
NM_181831.2:c.1142del	NP_861969.1:p.Ala381GlyfsTer21
NM_181832.2:c.1391del	NP_861970.1:p.Ala464GlyfsTer21
NM_181833.2:c.448-19866del	NP_861971.1:n.448-19866del
NR_156186.1:n.1950del
XM_017028809.2:c.1277del	XP_016884298.1:p.Ala426GlyfsTer21
XM_017028810.1:c.1277del	XP_016884299.1:p.Ala426GlyfsTer21
NM_000268.4:c.1391del MANE Select	NP_000259.1:p.Ala464GlyfsTer21
NM_181825.3:c.1391del	NP_861546.1:p.Ala464GlyfsTer21
NM_181828.3:c.1265del	NP_861966.1:p.Ala422GlyfsTer21
NM_181829.3:c.1268del	NP_861967.1:p.Ala423GlyfsTer21
NM_181830.3:c.1142del	NP_861968.1:p.Ala381GlyfsTer21
NM_181831.3:c.1142del	NP_861969.1:p.Ala381GlyfsTer21
NM_181832.3:c.1391del	NP_861970.1:p.Ala464GlyfsTer21
NR_156186.2:n.1873del
NM_181833.3:c.448-19866del	NP_861971.1:n.448-19866del