Canonical Allele Identifier: CA2400675742
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29655628G= , CM000684.2:g.29655628G= GRCh38
NC_000022.10:g.30051617G= , CM000684.1:g.30051617G= GRCh37
NC_000022.9:g.28381617G= NCBI36
NG_009057.1:g.57073G= , LRG_511:g.57073G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.551G= ENSP00000354529.6:p.Trp184=
ENST00000673312.2:c.*45G= ENSP00000500186.2:n.*45G=
ENST00000338641.10:c.551G= MANE Select ENSP00000344666.5:p.Trp184=
ENST00000361166.9:c.104G= ENSP00000354529.5:p.Trp35=
ENST00000672461.1:c.551G= ENSP00000500919.1:p.Trp184=
ENST00000672805.1:c.*433G= ENSP00000500295.1:n.*433G=
ENST00000672896.1:c.551G= ENSP00000500117.1:p.Trp184=
ENST00000673312.1:c.570G= ENSP00000500186.1:n.570G=
ENST00000334961.11:c.302G= ENSP00000335652.7:p.Trp101=
ENST00000338641.8:c.551G= ENSP00000344666.4:p.Trp184=
ENST00000353887.8:c.302G= ENSP00000340626.4:p.Trp101=
ENST00000361166.8:c.551G= ENSP00000354529.4:p.Trp184=
ENST00000361452.8:c.428G= ENSP00000354897.4:p.Trp143=
ENST00000361676.8:c.425G= ENSP00000355183.4:p.Trp142=
ENST00000397789.3:c.551G= ENSP00000380891.3:p.Trp184=
ENST00000403435.5:c.551G= ENSP00000384029.1:p.Trp184=
ENST00000403999.7:c.551G= ENSP00000384797.3:p.Trp184=
ENST00000413209.6:c.447+13343G= ENSP00000409921.2:n.447+13343G=
ENST00000432151.5:c.199-5577G= ENSP00000395885.1:n.199-5577G=
NM_000268.3:c.551G= , LRG_511t1:c.551G= NP_000259.1:p.Trp184=
NM_016418.5:c.551G= , LRG_511t2:c.551G= NP_057502.2:p.Trp184=
NM_181825.2:c.551G= NP_861546.1:p.Trp184=
NM_181828.2:c.425G= NP_861966.1:p.Trp142=
NM_181829.2:c.428G= NP_861967.1:p.Trp143=
NM_181830.2:c.302G= NP_861968.1:p.Trp101=
NM_181831.2:c.302G= NP_861969.1:p.Trp101=
NM_181832.2:c.551G= NP_861970.1:p.Trp184=
NM_181833.2:c.447+13343G= NP_861971.1:n.447+13343G=
NR_156186.1:n.1110G=
XM_017028809.2:c.437G= XP_016884298.1:p.Trp146=
XM_017028810.1:c.437G= XP_016884299.1:p.Trp146=
NM_000268.4:c.551G= MANE Select NP_000259.1:p.Trp184=
NM_181825.3:c.551G= NP_861546.1:p.Trp184=
NM_181828.3:c.425G= NP_861966.1:p.Trp142=
NM_181829.3:c.428G= NP_861967.1:p.Trp143=
NM_181830.3:c.302G= NP_861968.1:p.Trp101=
NM_181831.3:c.302G= NP_861969.1:p.Trp101=
NM_181832.3:c.551G= NP_861970.1:p.Trp184=
NR_156186.2:n.1033G=
NM_181833.3:c.447+13343G= NP_861971.1:n.447+13343G=