Canonical Allele Identifier: CA2400692338

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694885A= , CM000684.2:g.29694885A=	GRCh38
NC_000022.10:g.30090874A= , CM000684.1:g.30090874A=	GRCh37
NC_000022.9:g.28420874A=	NCBI36
NG_009057.1:g.96330A= , LRG_511:g.96330A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*83A=	ENSP00000354529.6:n.*83A=
ENST00000673312.2:c.*1365A=	ENSP00000500186.2:n.*1365A=
ENST00000338641.10:c.*83A= MANE Select	ENSP00000344666.5:n.*83A=
ENST00000361166.9:c.1289A=	ENSP00000354529.5:n.1289A=
ENST00000672461.1:c.*143A=	ENSP00000500919.1:n.*143A=
ENST00000672805.1:c.*1753A=	ENSP00000500295.1:n.*1753A=
ENST00000672896.1:c.*143A=	ENSP00000500117.1:n.*143A=
ENST00000673312.1:c.1890A=	ENSP00000500186.1:n.1890A=
ENST00000338641.8:c.*83A=	ENSP00000344666.4:n.*83A=
ENST00000361452.8:c.*143A=	ENSP00000354897.4:n.*143A=
ENST00000413209.6:c.*83A=	ENSP00000409921.2:n.*83A=
ENST00000432151.5:c.*227A=	ENSP00000395885.1:n.*227A=
NM_000268.3:c.*83A= , LRG_511t1:c.*83A=	NP_000259.1:n.*83A=
NM_016418.5:c.*143A= , LRG_511t2:c.*143A=	NP_057502.2:n.*143A=
NM_181828.2:c.*143A=	NP_861966.1:n.*143A=
NM_181829.2:c.*143A=	NP_861967.1:n.*143A=
NM_181830.2:c.*143A=	NP_861968.1:n.*143A=
NM_181832.2:c.*158A=	NP_861970.1:n.*158A=
NM_181833.2:c.*83A=	NP_861971.1:n.*83A=
NR_156186.1:n.2430A=
XM_017028809.2:c.*83A=	XP_016884298.1:n.*83A=
XM_017028810.1:c.*143A=	XP_016884299.1:n.*143A=
NM_000268.4:c.*83A= MANE Select	NP_000259.1:n.*83A=
NM_181828.3:c.*143A=	NP_861966.1:n.*143A=
NM_181829.3:c.*143A=	NP_861967.1:n.*143A=
NM_181830.3:c.*143A=	NP_861968.1:n.*143A=
NM_181832.3:c.*158A=	NP_861970.1:n.*158A=
NR_156186.2:n.2353A=
NM_181833.3:c.*83A=	NP_861971.1:n.*83A=