Canonical Allele Identifier: CA2400692518

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695252C= , CM000684.2:g.29695252C=	GRCh38
NC_000022.10:g.30091241C= , CM000684.1:g.30091241C=	GRCh37
NC_000022.9:g.28421241C=	NCBI36
NG_009057.1:g.96697C= , LRG_511:g.96697C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*450C= MANE Select	ENSP00000344666.5:n.*450C=
ENST00000672461.1:c.*501+9C=	ENSP00000500919.1:n.*501+9C=
ENST00000672896.1:c.*510C=	ENSP00000500117.1:n.*510C=
ENST00000338641.8:c.*450C=	ENSP00000344666.4:n.*450C=
ENST00000361452.8:c.*510C=	ENSP00000354897.4:n.*510C=
ENST00000413209.6:c.*450C=	ENSP00000409921.2:n.*450C=
NM_000268.3:c.*450C= , LRG_511t1:c.*450C=	NP_000259.1:n.*450C=
NM_016418.5:c.*510C= , LRG_511t2:c.*510C=	NP_057502.2:n.*510C=
NM_181828.2:c.*510C=	NP_861966.1:n.*510C=
NM_181829.2:c.*510C=	NP_861967.1:n.*510C=
NM_181830.2:c.*510C=	NP_861968.1:n.*510C=
NM_181832.2:c.*525C=	NP_861970.1:n.*525C=
NM_181833.2:c.*450C=	NP_861971.1:n.*450C=
NR_156186.1:n.2797C=
XM_017028810.1:c.*510C=	XP_016884299.1:n.*510C=
NM_000268.4:c.*450C= MANE Select	NP_000259.1:n.*450C=
NM_181828.3:c.*510C=	NP_861966.1:n.*510C=
NM_181829.3:c.*510C=	NP_861967.1:n.*510C=
NM_181830.3:c.*510C=	NP_861968.1:n.*510C=
NM_181832.3:c.*525C=	NP_861970.1:n.*525C=
NR_156186.2:n.2720C=
NM_181833.3:c.*450C=	NP_861971.1:n.*450C=