Canonical Allele Identifier: CA2400653195

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29603594G= , CM000684.2:g.29603594G=	GRCh38
NC_000022.10:g.29999583G= , CM000684.1:g.29999583G=	GRCh37
NC_000022.9:g.28329583G=	NCBI36
NG_009057.1:g.5039G= , LRG_511:g.5039G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000672805.1:c.-405G=	ENSP00000500295.1:n.-405G=
ENST00000338641.8:c.-405G=	ENSP00000344666.4:n.-405G=
ENST00000403435.5:c.-405G=	ENSP00000384029.1:n.-405G=
ENST00000413209.6:c.-405G=	ENSP00000409921.2:n.-405G=
NM_000268.3:c.-405G= , LRG_511t1:c.-405G=	NP_000259.1:n.-405G=
NM_016418.5:c.-405G= , LRG_511t2:c.-405G=	NP_057502.2:n.-405G=
NM_181825.2:c.-405G=	NP_861546.1:n.-405G=
NM_181828.2:c.-405G=	NP_861966.1:n.-405G=
NM_181829.2:c.-405G=	NP_861967.1:n.-405G=
NM_181830.2:c.-405G=	NP_861968.1:n.-405G=
NM_181831.2:c.-405G=	NP_861969.1:n.-405G=
NM_181832.2:c.-405G=	NP_861970.1:n.-405G=
NM_181833.2:c.-405G=	NP_861971.1:n.-405G=
NR_156186.1:n.39G=