Canonical Allele Identifier: CA2400692470

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695172A= , CM000684.2:g.29695172A=	GRCh38
NC_000022.10:g.30091161A= , CM000684.1:g.30091161A=	GRCh37
NC_000022.9:g.28421161A=	NCBI36
NG_009057.1:g.96617A= , LRG_511:g.96617A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*370A= MANE Select	ENSP00000344666.5:n.*370A=
ENST00000672461.1:c.*430A=	ENSP00000500919.1:n.*430A=
ENST00000672896.1:c.*430A=	ENSP00000500117.1:n.*430A=
ENST00000338641.8:c.*370A=	ENSP00000344666.4:n.*370A=
ENST00000361452.8:c.*430A=	ENSP00000354897.4:n.*430A=
ENST00000413209.6:c.*370A=	ENSP00000409921.2:n.*370A=
NM_000268.3:c.*370A= , LRG_511t1:c.*370A=	NP_000259.1:n.*370A=
NM_016418.5:c.*430A= , LRG_511t2:c.*430A=	NP_057502.2:n.*430A=
NM_181828.2:c.*430A=	NP_861966.1:n.*430A=
NM_181829.2:c.*430A=	NP_861967.1:n.*430A=
NM_181830.2:c.*430A=	NP_861968.1:n.*430A=
NM_181832.2:c.*445A=	NP_861970.1:n.*445A=
NM_181833.2:c.*370A=	NP_861971.1:n.*370A=
NR_156186.1:n.2717A=
XM_017028810.1:c.*430A=	XP_016884299.1:n.*430A=
NM_000268.4:c.*370A= MANE Select	NP_000259.1:n.*370A=
NM_181828.3:c.*430A=	NP_861966.1:n.*430A=
NM_181829.3:c.*430A=	NP_861967.1:n.*430A=
NM_181830.3:c.*430A=	NP_861968.1:n.*430A=
NM_181832.3:c.*445A=	NP_861970.1:n.*445A=
NR_156186.2:n.2640A=
NM_181833.3:c.*370A=	NP_861971.1:n.*370A=