Canonical Allele Identifier: CA2400693131
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29696584T= , CM000684.2:g.29696584T= GRCh38
NC_000022.10:g.30092573T= , CM000684.1:g.30092573T= GRCh37
NC_000022.9:g.28422573T= NCBI36
NG_009057.1:g.98029T= , LRG_511:g.98029T=

Transcript Alleles

HGVS Amino-acid change
ENST00000338641.10:c.*1782T= MANE Select ENSP00000344666.5:n.*1782T=
ENST00000672461.1:c.*502-677T= ENSP00000500919.1:n.*502-677T=
ENST00000672896.1:c.*1842T= ENSP00000500117.1:n.*1842T=
ENST00000338641.8:c.*1782T= ENSP00000344666.4:n.*1782T=
ENST00000361452.8:c.*1842T= ENSP00000354897.4:n.*1842T=
ENST00000413209.6:c.*1782T= ENSP00000409921.2:n.*1782T=
NM_000268.3:c.*1782T= , LRG_511t1:c.*1782T= NP_000259.1:n.*1782T=
NM_016418.5:c.*1842T= , LRG_511t2:c.*1842T= NP_057502.2:n.*1842T=
NM_181828.2:c.*1842T= NP_861966.1:n.*1842T=
NM_181829.2:c.*1842T= NP_861967.1:n.*1842T=
NM_181830.2:c.*1842T= NP_861968.1:n.*1842T=
NM_181832.2:c.*1857T= NP_861970.1:n.*1857T=
NM_181833.2:c.*1782T= NP_861971.1:n.*1782T=
NR_156186.1:n.4129T=
XM_017028810.1:c.*1842T= XP_016884299.1:n.*1842T=
NM_000268.4:c.*1782T= MANE Select NP_000259.1:n.*1782T=
NM_181828.3:c.*1842T= NP_861966.1:n.*1842T=
NM_181829.3:c.*1842T= NP_861967.1:n.*1842T=
NM_181830.3:c.*1842T= NP_861968.1:n.*1842T=
NM_181832.3:c.*1857T= NP_861970.1:n.*1857T=
NR_156186.2:n.4052T=
NM_181833.3:c.*1782T= NP_861971.1:n.*1782T=