Canonical Allele Identifier: CA2400692398

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695000T= , CM000684.2:g.29695000T=	GRCh38
NC_000022.10:g.30090989T= , CM000684.1:g.30090989T=	GRCh37
NC_000022.9:g.28420989T=	NCBI36
NG_009057.1:g.96445T= , LRG_511:g.96445T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*198T=	ENSP00000354529.6:n.*198T=
ENST00000673312.2:c.*1480T=	ENSP00000500186.2:n.*1480T=
ENST00000338641.10:c.*198T= MANE Select	ENSP00000344666.5:n.*198T=
ENST00000361166.9:c.1404T=	ENSP00000354529.5:n.1404T=
ENST00000672461.1:c.*258T=	ENSP00000500919.1:n.*258T=
ENST00000672896.1:c.*258T=	ENSP00000500117.1:n.*258T=
ENST00000673312.1:c.2005T=	ENSP00000500186.1:n.2005T=
ENST00000338641.8:c.*198T=	ENSP00000344666.4:n.*198T=
ENST00000361452.8:c.*258T=	ENSP00000354897.4:n.*258T=
ENST00000413209.6:c.*198T=	ENSP00000409921.2:n.*198T=
NM_000268.3:c.*198T= , LRG_511t1:c.*198T=	NP_000259.1:n.*198T=
NM_016418.5:c.*258T= , LRG_511t2:c.*258T=	NP_057502.2:n.*258T=
NM_181828.2:c.*258T=	NP_861966.1:n.*258T=
NM_181829.2:c.*258T=	NP_861967.1:n.*258T=
NM_181830.2:c.*258T=	NP_861968.1:n.*258T=
NM_181832.2:c.*273T=	NP_861970.1:n.*273T=
NM_181833.2:c.*198T=	NP_861971.1:n.*198T=
NR_156186.1:n.2545T=
XM_017028809.2:c.*198T=	XP_016884298.1:n.*198T=
XM_017028810.1:c.*258T=	XP_016884299.1:n.*258T=
NM_000268.4:c.*198T= MANE Select	NP_000259.1:n.*198T=
NM_181828.3:c.*258T=	NP_861966.1:n.*258T=
NM_181829.3:c.*258T=	NP_861967.1:n.*258T=
NM_181830.3:c.*258T=	NP_861968.1:n.*258T=
NM_181832.3:c.*273T=	NP_861970.1:n.*273T=
NR_156186.2:n.2468T=
NM_181833.3:c.*198T=	NP_861971.1:n.*198T=