Canonical Allele Identifier: CA2400692378

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694962T= , CM000684.2:g.29694962T=	GRCh38
NC_000022.10:g.30090951T= , CM000684.1:g.30090951T=	GRCh37
NC_000022.9:g.28420951T=	NCBI36
NG_009057.1:g.96407T= , LRG_511:g.96407T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*160T=	ENSP00000354529.6:n.*160T=
ENST00000673312.2:c.*1442T=	ENSP00000500186.2:n.*1442T=
ENST00000338641.10:c.*160T= MANE Select	ENSP00000344666.5:n.*160T=
ENST00000361166.9:c.1366T=	ENSP00000354529.5:n.1366T=
ENST00000672461.1:c.*220T=	ENSP00000500919.1:n.*220T=
ENST00000672896.1:c.*220T=	ENSP00000500117.1:n.*220T=
ENST00000673312.1:c.1967T=	ENSP00000500186.1:n.1967T=
ENST00000338641.8:c.*160T=	ENSP00000344666.4:n.*160T=
ENST00000361452.8:c.*220T=	ENSP00000354897.4:n.*220T=
ENST00000413209.6:c.*160T=	ENSP00000409921.2:n.*160T=
NM_000268.3:c.*160T= , LRG_511t1:c.*160T=	NP_000259.1:n.*160T=
NM_016418.5:c.*220T= , LRG_511t2:c.*220T=	NP_057502.2:n.*220T=
NM_181828.2:c.*220T=	NP_861966.1:n.*220T=
NM_181829.2:c.*220T=	NP_861967.1:n.*220T=
NM_181830.2:c.*220T=	NP_861968.1:n.*220T=
NM_181832.2:c.*235T=	NP_861970.1:n.*235T=
NM_181833.2:c.*160T=	NP_861971.1:n.*160T=
NR_156186.1:n.2507T=
XM_017028809.2:c.*160T=	XP_016884298.1:n.*160T=
XM_017028810.1:c.*220T=	XP_016884299.1:n.*220T=
NM_000268.4:c.*160T= MANE Select	NP_000259.1:n.*160T=
NM_181828.3:c.*220T=	NP_861966.1:n.*220T=
NM_181829.3:c.*220T=	NP_861967.1:n.*220T=
NM_181830.3:c.*220T=	NP_861968.1:n.*220T=
NM_181832.3:c.*235T=	NP_861970.1:n.*235T=
NR_156186.2:n.2430T=
NM_181833.3:c.*160T=	NP_861971.1:n.*160T=