Canonical Allele Identifier: CA2400692372

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694948C= , CM000684.2:g.29694948C=	GRCh38
NC_000022.10:g.30090937C= , CM000684.1:g.30090937C=	GRCh37
NC_000022.9:g.28420937C=	NCBI36
NG_009057.1:g.96393C= , LRG_511:g.96393C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*146C=	ENSP00000354529.6:n.*146C=
ENST00000673312.2:c.*1428C=	ENSP00000500186.2:n.*1428C=
ENST00000338641.10:c.*146C= MANE Select	ENSP00000344666.5:n.*146C=
ENST00000361166.9:c.1352C=	ENSP00000354529.5:n.1352C=
ENST00000672461.1:c.*206C=	ENSP00000500919.1:n.*206C=
ENST00000672896.1:c.*206C=	ENSP00000500117.1:n.*206C=
ENST00000673312.1:c.1953C=	ENSP00000500186.1:n.1953C=
ENST00000338641.8:c.*146C=	ENSP00000344666.4:n.*146C=
ENST00000361452.8:c.*206C=	ENSP00000354897.4:n.*206C=
ENST00000413209.6:c.*146C=	ENSP00000409921.2:n.*146C=
NM_000268.3:c.*146C= , LRG_511t1:c.*146C=	NP_000259.1:n.*146C=
NM_016418.5:c.*206C= , LRG_511t2:c.*206C=	NP_057502.2:n.*206C=
NM_181828.2:c.*206C=	NP_861966.1:n.*206C=
NM_181829.2:c.*206C=	NP_861967.1:n.*206C=
NM_181830.2:c.*206C=	NP_861968.1:n.*206C=
NM_181832.2:c.*221C=	NP_861970.1:n.*221C=
NM_181833.2:c.*146C=	NP_861971.1:n.*146C=
NR_156186.1:n.2493C=
XM_017028809.2:c.*146C=	XP_016884298.1:n.*146C=
XM_017028810.1:c.*206C=	XP_016884299.1:n.*206C=
NM_000268.4:c.*146C= MANE Select	NP_000259.1:n.*146C=
NM_181828.3:c.*206C=	NP_861966.1:n.*206C=
NM_181829.3:c.*206C=	NP_861967.1:n.*206C=
NM_181830.3:c.*206C=	NP_861968.1:n.*206C=
NM_181832.3:c.*221C=	NP_861970.1:n.*221C=
NR_156186.2:n.2416C=
NM_181833.3:c.*146C=	NP_861971.1:n.*146C=