Canonical Allele Identifier: CA2400692381

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694978T= , CM000684.2:g.29694978T=	GRCh38
NC_000022.10:g.30090967T= , CM000684.1:g.30090967T=	GRCh37
NC_000022.9:g.28420967T=	NCBI36
NG_009057.1:g.96423T= , LRG_511:g.96423T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*176T=	ENSP00000354529.6:n.*176T=
ENST00000673312.2:c.*1458T=	ENSP00000500186.2:n.*1458T=
ENST00000338641.10:c.*176T= MANE Select	ENSP00000344666.5:n.*176T=
ENST00000361166.9:c.1382T=	ENSP00000354529.5:n.1382T=
ENST00000672461.1:c.*236T=	ENSP00000500919.1:n.*236T=
ENST00000672896.1:c.*236T=	ENSP00000500117.1:n.*236T=
ENST00000673312.1:c.1983T=	ENSP00000500186.1:n.1983T=
ENST00000338641.8:c.*176T=	ENSP00000344666.4:n.*176T=
ENST00000361452.8:c.*236T=	ENSP00000354897.4:n.*236T=
ENST00000413209.6:c.*176T=	ENSP00000409921.2:n.*176T=
NM_000268.3:c.*176T= , LRG_511t1:c.*176T=	NP_000259.1:n.*176T=
NM_016418.5:c.*236T= , LRG_511t2:c.*236T=	NP_057502.2:n.*236T=
NM_181828.2:c.*236T=	NP_861966.1:n.*236T=
NM_181829.2:c.*236T=	NP_861967.1:n.*236T=
NM_181830.2:c.*236T=	NP_861968.1:n.*236T=
NM_181832.2:c.*251T=	NP_861970.1:n.*251T=
NM_181833.2:c.*176T=	NP_861971.1:n.*176T=
NR_156186.1:n.2523T=
XM_017028809.2:c.*176T=	XP_016884298.1:n.*176T=
XM_017028810.1:c.*236T=	XP_016884299.1:n.*236T=
NM_000268.4:c.*176T= MANE Select	NP_000259.1:n.*176T=
NM_181828.3:c.*236T=	NP_861966.1:n.*236T=
NM_181829.3:c.*236T=	NP_861967.1:n.*236T=
NM_181830.3:c.*236T=	NP_861968.1:n.*236T=
NM_181832.3:c.*251T=	NP_861970.1:n.*251T=
NR_156186.2:n.2446T=
NM_181833.3:c.*176T=	NP_861971.1:n.*176T=