Canonical Allele Identifier: CA2400692405
Gene: NF2 HGNC NCBI

Linked Data

dbSNP Id: rs1035299560

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29695007G>C , CM000684.2:g.29695007G>C GRCh38
NC_000022.10:g.30090996G>C , CM000684.1:g.30090996G>C GRCh37
NC_000022.9:g.28420996G>C NCBI36
NG_009057.1:g.96452G>C , LRG_511:g.96452G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.*205G>C ENSP00000354529.6:n.*205G>C
ENST00000673312.2:c.*1487G>C ENSP00000500186.2:n.*1487G>C
ENST00000338641.10:c.*205G>C MANE Select ENSP00000344666.5:n.*205G>C
ENST00000361166.9:c.1411G>C ENSP00000354529.5:n.1411G>C
ENST00000672461.1:c.*265G>C ENSP00000500919.1:n.*265G>C
ENST00000672896.1:c.*265G>C ENSP00000500117.1:n.*265G>C
ENST00000673312.1:c.2012G>C ENSP00000500186.1:n.2012G>C
ENST00000338641.8:c.*205G>C ENSP00000344666.4:n.*205G>C
ENST00000361452.8:c.*265G>C ENSP00000354897.4:n.*265G>C
ENST00000413209.6:c.*205G>C ENSP00000409921.2:n.*205G>C
NM_000268.3:c.*205G>C , LRG_511t1:c.*205G>C NP_000259.1:n.*205G>C
NM_016418.5:c.*265G>C , LRG_511t2:c.*265G>C NP_057502.2:n.*265G>C
NM_181828.2:c.*265G>C NP_861966.1:n.*265G>C
NM_181829.2:c.*265G>C NP_861967.1:n.*265G>C
NM_181830.2:c.*265G>C NP_861968.1:n.*265G>C
NM_181832.2:c.*280G>C NP_861970.1:n.*280G>C
NM_181833.2:c.*205G>C NP_861971.1:n.*205G>C
NR_156186.1:n.2552G>C
XM_017028809.2:c.*205G>C XP_016884298.1:n.*205G>C
XM_017028810.1:c.*265G>C XP_016884299.1:n.*265G>C
NM_000268.4:c.*205G>C MANE Select NP_000259.1:n.*205G>C
NM_181828.3:c.*265G>C NP_861966.1:n.*265G>C
NM_181829.3:c.*265G>C NP_861967.1:n.*265G>C
NM_181830.3:c.*265G>C NP_861968.1:n.*265G>C
NM_181832.3:c.*280G>C NP_861970.1:n.*280G>C
NR_156186.2:n.2475G>C
NM_181833.3:c.*205G>C NP_861971.1:n.*205G>C