Canonical Allele Identifier: CA2400692406

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695011T= , CM000684.2:g.29695011T=	GRCh38
NC_000022.10:g.30091000T= , CM000684.1:g.30091000T=	GRCh37
NC_000022.9:g.28421000T=	NCBI36
NG_009057.1:g.96456T= , LRG_511:g.96456T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.*209T=	ENSP00000354529.6:n.*209T=
ENST00000673312.2:c.*1491T=	ENSP00000500186.2:n.*1491T=
ENST00000338641.10:c.*209T= MANE Select	ENSP00000344666.5:n.*209T=
ENST00000361166.9:c.1415T=	ENSP00000354529.5:n.1415T=
ENST00000672461.1:c.*269T=	ENSP00000500919.1:n.*269T=
ENST00000672896.1:c.*269T=	ENSP00000500117.1:n.*269T=
ENST00000673312.1:c.2016T=	ENSP00000500186.1:n.2016T=
ENST00000338641.8:c.*209T=	ENSP00000344666.4:n.*209T=
ENST00000361452.8:c.*269T=	ENSP00000354897.4:n.*269T=
ENST00000413209.6:c.*209T=	ENSP00000409921.2:n.*209T=
NM_000268.3:c.*209T= , LRG_511t1:c.*209T=	NP_000259.1:n.*209T=
NM_016418.5:c.*269T= , LRG_511t2:c.*269T=	NP_057502.2:n.*269T=
NM_181828.2:c.*269T=	NP_861966.1:n.*269T=
NM_181829.2:c.*269T=	NP_861967.1:n.*269T=
NM_181830.2:c.*269T=	NP_861968.1:n.*269T=
NM_181832.2:c.*284T=	NP_861970.1:n.*284T=
NM_181833.2:c.*209T=	NP_861971.1:n.*209T=
NR_156186.1:n.2556T=
XM_017028809.2:c.*209T=	XP_016884298.1:n.*209T=
XM_017028810.1:c.*269T=	XP_016884299.1:n.*269T=
NM_000268.4:c.*209T= MANE Select	NP_000259.1:n.*209T=
NM_181828.3:c.*269T=	NP_861966.1:n.*269T=
NM_181829.3:c.*269T=	NP_861967.1:n.*269T=
NM_181830.3:c.*269T=	NP_861968.1:n.*269T=
NM_181832.3:c.*284T=	NP_861970.1:n.*284T=
NR_156186.2:n.2479T=
NM_181833.3:c.*209T=	NP_861971.1:n.*209T=