Canonical Allele Identifier: CA2400685430
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29678276C= , CM000684.2:g.29678276C= GRCh38
NC_000022.10:g.30074265C= , CM000684.1:g.30074265C= GRCh37
NC_000022.9:g.28404265C= NCBI36
NG_009057.1:g.79721C= , LRG_511:g.79721C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.1392C= ENSP00000354529.6:p.Phe464=
ENST00000673312.2:c.*1021C= ENSP00000500186.2:n.*1021C=
ENST00000338641.10:c.1527C= MANE Select ENSP00000344666.5:p.Phe509=
ENST00000361166.9:c.945C= ENSP00000354529.5:p.Phe315=
ENST00000672461.1:c.1527C= ENSP00000500919.1:p.Phe509=
ENST00000672805.1:c.*1409C= ENSP00000500295.1:n.*1409C=
ENST00000672896.1:c.1527C= ENSP00000500117.1:p.Phe509=
ENST00000673312.1:c.1546C= ENSP00000500186.1:n.1546C=
ENST00000334961.11:c.1278C= ENSP00000335652.7:p.Phe426=
ENST00000338641.8:c.1527C= ENSP00000344666.4:p.Phe509=
ENST00000353887.8:c.1278C= ENSP00000340626.4:p.Phe426=
ENST00000361166.8:c.1527C= ENSP00000354529.4:p.Phe509=
ENST00000361452.8:c.1404C= ENSP00000354897.4:p.Phe468=
ENST00000361676.8:c.1401C= ENSP00000355183.4:p.Phe467=
ENST00000397789.3:c.1527C= ENSP00000380891.3:p.Phe509=
ENST00000403435.5:c.1440C= ENSP00000384029.1:p.Phe480=
ENST00000403999.7:c.1527C= ENSP00000384797.3:p.Phe509=
ENST00000413209.6:c.448-16476C= ENSP00000409921.2:n.448-16476C=
ENST00000432151.5:c.*46C= ENSP00000395885.1:n.*46C=
NM_000268.3:c.1527C= , LRG_511t1:c.1527C= NP_000259.1:p.Phe509=
NM_016418.5:c.1527C= , LRG_511t2:c.1527C= NP_057502.2:p.Phe509=
NM_181825.2:c.1527C= NP_861546.1:p.Phe509=
NM_181828.2:c.1401C= NP_861966.1:p.Phe467=
NM_181829.2:c.1404C= NP_861967.1:p.Phe468=
NM_181830.2:c.1278C= NP_861968.1:p.Phe426=
NM_181831.2:c.1278C= NP_861969.1:p.Phe426=
NM_181832.2:c.1527C= NP_861970.1:p.Phe509=
NM_181833.2:c.448-16476C= NP_861971.1:n.448-16476C=
NR_156186.1:n.2086C=
XM_017028809.2:c.1413C= XP_016884298.1:p.Phe471=
XM_017028810.1:c.1413C= XP_016884299.1:p.Phe471=
NM_000268.4:c.1527C= MANE Select NP_000259.1:p.Phe509=
NM_181825.3:c.1527C= NP_861546.1:p.Phe509=
NM_181828.3:c.1401C= NP_861966.1:p.Phe467=
NM_181829.3:c.1404C= NP_861967.1:p.Phe468=
NM_181830.3:c.1278C= NP_861968.1:p.Phe426=
NM_181831.3:c.1278C= NP_861969.1:p.Phe426=
NM_181832.3:c.1527C= NP_861970.1:p.Phe509=
NR_156186.2:n.2009C=
NM_181833.3:c.448-16476C= NP_861971.1:n.448-16476C=