Canonical Allele Identifier: CA2400693408

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29697138T= , CM000684.2:g.29697138T=	GRCh38
NC_000022.10:g.30093127T= , CM000684.1:g.30093127T=	GRCh37
NC_000022.9:g.28423127T=	NCBI36
NG_009057.1:g.98583T= , LRG_511:g.98583T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*2336T= MANE Select	ENSP00000344666.5:n.*2336T=
ENST00000672461.1:c.*502-123T=	ENSP00000500919.1:n.*502-123T=
ENST00000672896.1:c.*2396T=	ENSP00000500117.1:n.*2396T=
ENST00000338641.8:c.*2336T=	ENSP00000344666.4:n.*2336T=
ENST00000361452.8:c.*2396T=	ENSP00000354897.4:n.*2396T=
ENST00000413209.6:c.*2336T=	ENSP00000409921.2:n.*2336T=
NM_000268.3:c.*2336T= , LRG_511t1:c.*2336T=	NP_000259.1:n.*2336T=
NM_016418.5:c.*2396T= , LRG_511t2:c.*2396T=	NP_057502.2:n.*2396T=
NM_181828.2:c.*2396T=	NP_861966.1:n.*2396T=
NM_181829.2:c.*2396T=	NP_861967.1:n.*2396T=
NM_181830.2:c.*2396T=	NP_861968.1:n.*2396T=
NM_181832.2:c.*2411T=	NP_861970.1:n.*2411T=
NM_181833.2:c.*2336T=	NP_861971.1:n.*2336T=
NR_156186.1:n.4683T=
XM_017028810.1:c.*2396T=	XP_016884299.1:n.*2396T=
NM_000268.4:c.*2336T= MANE Select	NP_000259.1:n.*2336T=
NM_181828.3:c.*2396T=	NP_861966.1:n.*2396T=
NM_181829.3:c.*2396T=	NP_861967.1:n.*2396T=
NM_181830.3:c.*2396T=	NP_861968.1:n.*2396T=
NM_181832.3:c.*2411T=	NP_861970.1:n.*2411T=
NR_156186.2:n.4606T=
NM_181833.3:c.*2336T=	NP_861971.1:n.*2336T=