Canonical Allele Identifier: CA2400686799

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29681443G= , CM000684.2:g.29681443G=	GRCh38
NC_000022.10:g.30077432G= , CM000684.1:g.30077432G=	GRCh37
NC_000022.9:g.28407432G=	NCBI36
NG_009057.1:g.82888G= , LRG_511:g.82888G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000268.4:c.1579G= MANE Select	NP_000259.1:p.Glu527=
ENST00000338641.10:c.1579G= MANE Select	ENSP00000344666.5:p.Glu527=
NM_000268.3:c.1579G= , LRG_511t1:c.1579G=	NP_000259.1:p.Glu527=
NM_016418.5:c.1579G= , LRG_511t2:c.1579G=	NP_057502.2:p.Glu527=
NM_181825.2:c.1579G=	NP_861546.1:p.Glu527=
NM_181825.3:c.1579G=	NP_861546.1:p.Glu527=
NM_181828.2:c.1453G=	NP_861966.1:p.Glu485=
NM_181828.3:c.1453G=	NP_861966.1:p.Glu485=
NM_181829.2:c.1456G=	NP_861967.1:p.Glu486=
NM_181829.3:c.1456G=	NP_861967.1:p.Glu486=
NM_181830.2:c.1330G=	NP_861968.1:p.Glu444=
NM_181830.3:c.1330G=	NP_861968.1:p.Glu444=
NM_181831.2:c.1330G=	NP_861969.1:p.Glu444=
NM_181831.3:c.1330G=	NP_861969.1:p.Glu444=
NM_181832.2:c.1579G=	NP_861970.1:p.Glu527=
NM_181832.3:c.1579G=	NP_861970.1:p.Glu527=
NM_181833.2:c.448-13309G=	NP_861971.1:n.448-13309G=
NM_181833.3:c.448-13309G=	NP_861971.1:n.448-13309G=
NR_156186.1:n.2138G=
NR_156186.2:n.2061G=
ENST00000334961.11:c.1330G=	ENSP00000335652.7:p.Glu444=
ENST00000338641.8:c.1579G=	ENSP00000344666.4:p.Glu527=
ENST00000353887.8:c.1330G=	ENSP00000340626.4:p.Glu444=
ENST00000361166.10:c.1444G=	ENSP00000354529.6:p.Glu482=
ENST00000361166.8:c.1579G=	ENSP00000354529.4:p.Glu527=
ENST00000361166.9:c.997G=	ENSP00000354529.5:p.Glu333=
ENST00000361452.8:c.1456G=	ENSP00000354897.4:p.Glu486=
ENST00000361676.8:c.1453G=	ENSP00000355183.4:p.Glu485=
ENST00000397789.3:c.1579G=	ENSP00000380891.3:p.Glu527=
ENST00000403435.5:c.1492G=	ENSP00000384029.1:p.Glu498=
ENST00000403999.7:c.1579G=	ENSP00000384797.3:p.Glu527=
ENST00000413209.6:c.448-13309G=	ENSP00000409921.2:n.448-13309G=
ENST00000432151.5:c.*93+3120G=	ENSP00000395885.1:n.*93+3120G=
ENST00000672461.1:c.1579G=	ENSP00000500919.1:p.Glu527=
ENST00000672805.1:c.*1461G=	ENSP00000500295.1:n.*1461G=
ENST00000672896.1:c.1579G=	ENSP00000500117.1:p.Glu527=
ENST00000673312.1:c.1598G=	ENSP00000500186.1:n.1598G=
ENST00000673312.2:c.*1073G=	ENSP00000500186.2:n.*1073G=
XM_017028809.2:c.1465G=	XP_016884298.1:p.Glu489=
XM_017028810.1:c.1465G=	XP_016884299.1:p.Glu489=