Canonical Allele Identifier: CA2400692666

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695556G= , CM000684.2:g.29695556G=	GRCh38
NC_000022.10:g.30091545G= , CM000684.1:g.30091545G=	GRCh37
NC_000022.9:g.28421545G=	NCBI36
NG_009057.1:g.97001G= , LRG_511:g.97001G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*754G= MANE Select	ENSP00000344666.5:n.*754G=
ENST00000672461.1:c.*501+313G=	ENSP00000500919.1:n.*501+313G=
ENST00000672896.1:c.*814G=	ENSP00000500117.1:n.*814G=
ENST00000338641.8:c.*754G=	ENSP00000344666.4:n.*754G=
ENST00000361452.8:c.*814G=	ENSP00000354897.4:n.*814G=
ENST00000413209.6:c.*754G=	ENSP00000409921.2:n.*754G=
NM_000268.3:c.*754G= , LRG_511t1:c.*754G=	NP_000259.1:n.*754G=
NM_016418.5:c.*814G= , LRG_511t2:c.*814G=	NP_057502.2:n.*814G=
NM_181828.2:c.*814G=	NP_861966.1:n.*814G=
NM_181829.2:c.*814G=	NP_861967.1:n.*814G=
NM_181830.2:c.*814G=	NP_861968.1:n.*814G=
NM_181832.2:c.*829G=	NP_861970.1:n.*829G=
NM_181833.2:c.*754G=	NP_861971.1:n.*754G=
NR_156186.1:n.3101G=
XM_017028810.1:c.*814G=	XP_016884299.1:n.*814G=
NM_000268.4:c.*754G= MANE Select	NP_000259.1:n.*754G=
NM_181828.3:c.*814G=	NP_861966.1:n.*814G=
NM_181829.3:c.*814G=	NP_861967.1:n.*814G=
NM_181830.3:c.*814G=	NP_861968.1:n.*814G=
NM_181832.3:c.*829G=	NP_861970.1:n.*829G=
NR_156186.2:n.3024G=
NM_181833.3:c.*754G=	NP_861971.1:n.*754G=