Canonical Allele Identifier: CA2400693348

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29697014G= , CM000684.2:g.29697014G=	GRCh38
NC_000022.10:g.30093003G= , CM000684.1:g.30093003G=	GRCh37
NC_000022.9:g.28423003G=	NCBI36
NG_009057.1:g.98459G= , LRG_511:g.98459G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*2212G= MANE Select	ENSP00000344666.5:n.*2212G=
ENST00000672461.1:c.*502-247G=	ENSP00000500919.1:n.*502-247G=
ENST00000672896.1:c.*2272G=	ENSP00000500117.1:n.*2272G=
ENST00000338641.8:c.*2212G=	ENSP00000344666.4:n.*2212G=
ENST00000361452.8:c.*2272G=	ENSP00000354897.4:n.*2272G=
ENST00000413209.6:c.*2212G=	ENSP00000409921.2:n.*2212G=
NM_000268.3:c.*2212G= , LRG_511t1:c.*2212G=	NP_000259.1:n.*2212G=
NM_016418.5:c.*2272G= , LRG_511t2:c.*2272G=	NP_057502.2:n.*2272G=
NM_181828.2:c.*2272G=	NP_861966.1:n.*2272G=
NM_181829.2:c.*2272G=	NP_861967.1:n.*2272G=
NM_181830.2:c.*2272G=	NP_861968.1:n.*2272G=
NM_181832.2:c.*2287G=	NP_861970.1:n.*2287G=
NM_181833.2:c.*2212G=	NP_861971.1:n.*2212G=
NR_156186.1:n.4559G=
XM_017028810.1:c.*2272G=	XP_016884299.1:n.*2272G=
NM_000268.4:c.*2212G= MANE Select	NP_000259.1:n.*2212G=
NM_181828.3:c.*2272G=	NP_861966.1:n.*2272G=
NM_181829.3:c.*2272G=	NP_861967.1:n.*2272G=
NM_181830.3:c.*2272G=	NP_861968.1:n.*2272G=
NM_181832.3:c.*2287G=	NP_861970.1:n.*2287G=
NR_156186.2:n.4482G=
NM_181833.3:c.*2212G=	NP_861971.1:n.*2212G=