Canonical Allele Identifier: CA2400692595

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695411G= , CM000684.2:g.29695411G=	GRCh38
NC_000022.10:g.30091400G= , CM000684.1:g.30091400G=	GRCh37
NC_000022.9:g.28421400G=	NCBI36
NG_009057.1:g.96856G= , LRG_511:g.96856G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*609G= MANE Select	ENSP00000344666.5:n.*609G=
ENST00000672461.1:c.*501+168G=	ENSP00000500919.1:n.*501+168G=
ENST00000672896.1:c.*669G=	ENSP00000500117.1:n.*669G=
ENST00000338641.8:c.*609G=	ENSP00000344666.4:n.*609G=
ENST00000361452.8:c.*669G=	ENSP00000354897.4:n.*669G=
ENST00000413209.6:c.*609G=	ENSP00000409921.2:n.*609G=
NM_000268.3:c.*609G= , LRG_511t1:c.*609G=	NP_000259.1:n.*609G=
NM_016418.5:c.*669G= , LRG_511t2:c.*669G=	NP_057502.2:n.*669G=
NM_181828.2:c.*669G=	NP_861966.1:n.*669G=
NM_181829.2:c.*669G=	NP_861967.1:n.*669G=
NM_181830.2:c.*669G=	NP_861968.1:n.*669G=
NM_181832.2:c.*684G=	NP_861970.1:n.*684G=
NM_181833.2:c.*609G=	NP_861971.1:n.*609G=
NR_156186.1:n.2956G=
XM_017028810.1:c.*669G=	XP_016884299.1:n.*669G=
NM_000268.4:c.*609G= MANE Select	NP_000259.1:n.*609G=
NM_181828.3:c.*669G=	NP_861966.1:n.*669G=
NM_181829.3:c.*669G=	NP_861967.1:n.*669G=
NM_181830.3:c.*669G=	NP_861968.1:n.*669G=
NM_181832.3:c.*684G=	NP_861970.1:n.*684G=
NR_156186.2:n.2879G=
NM_181833.3:c.*609G=	NP_861971.1:n.*609G=