Canonical Allele Identifier: CA2400692359
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29694925T= , CM000684.2:g.29694925T= GRCh38
NC_000022.10:g.30090914T= , CM000684.1:g.30090914T= GRCh37
NC_000022.9:g.28420914T= NCBI36
NG_009057.1:g.96370T= , LRG_511:g.96370T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.*123T= ENSP00000354529.6:n.*123T=
ENST00000673312.2:c.*1405T= ENSP00000500186.2:n.*1405T=
ENST00000338641.10:c.*123T= MANE Select ENSP00000344666.5:n.*123T=
ENST00000361166.9:c.1329T= ENSP00000354529.5:n.1329T=
ENST00000672461.1:c.*183T= ENSP00000500919.1:n.*183T=
ENST00000672805.1:c.*1793T= ENSP00000500295.1:n.*1793T=
ENST00000672896.1:c.*183T= ENSP00000500117.1:n.*183T=
ENST00000673312.1:c.1930T= ENSP00000500186.1:n.1930T=
ENST00000338641.8:c.*123T= ENSP00000344666.4:n.*123T=
ENST00000361452.8:c.*183T= ENSP00000354897.4:n.*183T=
ENST00000413209.6:c.*123T= ENSP00000409921.2:n.*123T=
ENST00000432151.5:c.*267T= ENSP00000395885.1:n.*267T=
NM_000268.3:c.*123T= , LRG_511t1:c.*123T= NP_000259.1:n.*123T=
NM_016418.5:c.*183T= , LRG_511t2:c.*183T= NP_057502.2:n.*183T=
NM_181828.2:c.*183T= NP_861966.1:n.*183T=
NM_181829.2:c.*183T= NP_861967.1:n.*183T=
NM_181830.2:c.*183T= NP_861968.1:n.*183T=
NM_181832.2:c.*198T= NP_861970.1:n.*198T=
NM_181833.2:c.*123T= NP_861971.1:n.*123T=
NR_156186.1:n.2470T=
XM_017028809.2:c.*123T= XP_016884298.1:n.*123T=
XM_017028810.1:c.*183T= XP_016884299.1:n.*183T=
NM_000268.4:c.*123T= MANE Select NP_000259.1:n.*123T=
NM_181828.3:c.*183T= NP_861966.1:n.*183T=
NM_181829.3:c.*183T= NP_861967.1:n.*183T=
NM_181830.3:c.*183T= NP_861968.1:n.*183T=
NM_181832.3:c.*198T= NP_861970.1:n.*198T=
NR_156186.2:n.2393T=
NM_181833.3:c.*123T= NP_861971.1:n.*123T=