Canonical Allele Identifier: CA2695202037
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29696067T= , CM000684.2:g.29696067T= GRCh38
NC_000022.10:g.30092056T= , CM000684.1:g.30092056T= GRCh37
NC_000022.9:g.28422056T= NCBI36
NG_009057.1:g.97512T= , LRG_511:g.97512T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338641.10:c.*1265T= MANE Select ENSP00000344666.5:n.*1265T=
ENST00000672461.1:c.*501+824T= ENSP00000500919.1:n.*501+824T=
ENST00000672896.1:c.*1325T= ENSP00000500117.1:n.*1325T=
ENST00000338641.8:c.*1265T= ENSP00000344666.4:n.*1265T=
ENST00000361452.8:c.*1325T= ENSP00000354897.4:n.*1325T=
ENST00000413209.6:c.*1265T= ENSP00000409921.2:n.*1265T=
NM_000268.3:c.*1265T= , LRG_511t1:c.*1265T= NP_000259.1:n.*1265T=
NM_016418.5:c.*1325T= , LRG_511t2:c.*1325T= NP_057502.2:n.*1325T=
NM_181828.2:c.*1325T= NP_861966.1:n.*1325T=
NM_181829.2:c.*1325T= NP_861967.1:n.*1325T=
NM_181830.2:c.*1325T= NP_861968.1:n.*1325T=
NM_181832.2:c.*1340T= NP_861970.1:n.*1340T=
NM_181833.2:c.*1265T= NP_861971.1:n.*1265T=
NR_156186.1:n.3612T=
XM_017028810.1:c.*1325T= XP_016884299.1:n.*1325T=
NM_000268.4:c.*1265T= MANE Select NP_000259.1:n.*1265T=
NM_181828.3:c.*1325T= NP_861966.1:n.*1325T=
NM_181829.3:c.*1325T= NP_861967.1:n.*1325T=
NM_181830.3:c.*1325T= NP_861968.1:n.*1325T=
NM_181832.3:c.*1340T= NP_861970.1:n.*1340T=
NR_156186.2:n.3535T=
NM_181833.3:c.*1265T= NP_861971.1:n.*1265T=