Canonical Allele Identifier: CA2400693340

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29696991A= , CM000684.2:g.29696991A=	GRCh38
NC_000022.10:g.30092980A= , CM000684.1:g.30092980A=	GRCh37
NC_000022.9:g.28422980A=	NCBI36
NG_009057.1:g.98436A= , LRG_511:g.98436A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*2189A= MANE Select	ENSP00000344666.5:n.*2189A=
ENST00000672461.1:c.*502-270A=	ENSP00000500919.1:n.*502-270A=
ENST00000672896.1:c.*2249A=	ENSP00000500117.1:n.*2249A=
ENST00000338641.8:c.*2189A=	ENSP00000344666.4:n.*2189A=
ENST00000361452.8:c.*2249A=	ENSP00000354897.4:n.*2249A=
ENST00000413209.6:c.*2189A=	ENSP00000409921.2:n.*2189A=
NM_000268.3:c.*2189A= , LRG_511t1:c.*2189A=	NP_000259.1:n.*2189A=
NM_016418.5:c.*2249A= , LRG_511t2:c.*2249A=	NP_057502.2:n.*2249A=
NM_181828.2:c.*2249A=	NP_861966.1:n.*2249A=
NM_181829.2:c.*2249A=	NP_861967.1:n.*2249A=
NM_181830.2:c.*2249A=	NP_861968.1:n.*2249A=
NM_181832.2:c.*2264A=	NP_861970.1:n.*2264A=
NM_181833.2:c.*2189A=	NP_861971.1:n.*2189A=
NR_156186.1:n.4536A=
XM_017028810.1:c.*2249A=	XP_016884299.1:n.*2249A=
NM_000268.4:c.*2189A= MANE Select	NP_000259.1:n.*2189A=
NM_181828.3:c.*2249A=	NP_861966.1:n.*2249A=
NM_181829.3:c.*2249A=	NP_861967.1:n.*2249A=
NM_181830.3:c.*2249A=	NP_861968.1:n.*2249A=
NM_181832.3:c.*2264A=	NP_861970.1:n.*2264A=
NR_156186.2:n.4459A=
NM_181833.3:c.*2189A=	NP_861971.1:n.*2189A=