Canonical Allele Identifier: CA2400692493

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695209C= , CM000684.2:g.29695209C=	GRCh38
NC_000022.10:g.30091198C= , CM000684.1:g.30091198C=	GRCh37
NC_000022.9:g.28421198C=	NCBI36
NG_009057.1:g.96654C= , LRG_511:g.96654C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*407C= MANE Select	ENSP00000344666.5:n.*407C=
ENST00000672461.1:c.*467C=	ENSP00000500919.1:n.*467C=
ENST00000672896.1:c.*467C=	ENSP00000500117.1:n.*467C=
ENST00000338641.8:c.*407C=	ENSP00000344666.4:n.*407C=
ENST00000361452.8:c.*467C=	ENSP00000354897.4:n.*467C=
ENST00000413209.6:c.*407C=	ENSP00000409921.2:n.*407C=
NM_000268.3:c.*407C= , LRG_511t1:c.*407C=	NP_000259.1:n.*407C=
NM_016418.5:c.*467C= , LRG_511t2:c.*467C=	NP_057502.2:n.*467C=
NM_181828.2:c.*467C=	NP_861966.1:n.*467C=
NM_181829.2:c.*467C=	NP_861967.1:n.*467C=
NM_181830.2:c.*467C=	NP_861968.1:n.*467C=
NM_181832.2:c.*482C=	NP_861970.1:n.*482C=
NM_181833.2:c.*407C=	NP_861971.1:n.*407C=
NR_156186.1:n.2754C=
XM_017028810.1:c.*467C=	XP_016884299.1:n.*467C=
NM_000268.4:c.*407C= MANE Select	NP_000259.1:n.*407C=
NM_181828.3:c.*467C=	NP_861966.1:n.*467C=
NM_181829.3:c.*467C=	NP_861967.1:n.*467C=
NM_181830.3:c.*467C=	NP_861968.1:n.*467C=
NM_181832.3:c.*482C=	NP_861970.1:n.*482C=
NR_156186.2:n.2677C=
NM_181833.3:c.*407C=	NP_861971.1:n.*407C=