Canonical Allele Identifier: CA021406
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3297
ClinVar RCV Id: RCV000003458
dbSNP Id: rs121434261

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29636821T>C , CM000684.2:g.29636821T>C GRCh38
NC_000022.10:g.30032810T>C , CM000684.1:g.30032810T>C GRCh37
NC_000022.9:g.28362810T>C NCBI36
NG_009057.1:g.38266T>C , LRG_511:g.38266T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361166.10:c.185T>C ENSP00000354529.6:p.Phe62Ser
ENST00000673312.2:c.185T>C ENSP00000500186.2:p.Phe62Ser
ENST00000338641.10:c.185T>C MANE Select ENSP00000344666.5:p.Phe62Ser
ENST00000672461.1:c.185T>C ENSP00000500919.1:p.Phe62Ser
ENST00000672805.1:c.*67T>C ENSP00000500295.1:n.*67T>C
ENST00000672896.1:c.185T>C ENSP00000500117.1:p.Phe62Ser
ENST00000673312.1:c.98T>C ENSP00000500186.1:p.Phe33Ser
ENST00000334961.11:c.115-5381T>C ENSP00000335652.7:n.115-5381T>C
ENST00000338641.8:c.185T>C ENSP00000344666.4:p.Phe62Ser
ENST00000353887.8:c.115-5381T>C ENSP00000340626.4:n.115-5381T>C
ENST00000361166.8:c.185T>C ENSP00000354529.4:p.Phe62Ser
ENST00000361452.8:c.185T>C ENSP00000354897.4:p.Phe62Ser
ENST00000361676.8:c.115-2269T>C ENSP00000355183.4:n.115-2269T>C
ENST00000397789.3:c.185T>C ENSP00000380891.3:p.Phe62Ser
ENST00000403435.5:c.185T>C ENSP00000384029.1:p.Phe62Ser
ENST00000403999.7:c.185T>C ENSP00000384797.3:p.Phe62Ser
ENST00000413209.6:c.185T>C ENSP00000409921.2:p.Phe62Ser
ENST00000432151.5:c.115-5381T>C ENSP00000395885.1:n.115-5381T>C
NM_000268.3:c.185T>C , LRG_511t1:c.185T>C NP_000259.1:p.Phe62Ser
NM_016418.5:c.185T>C , LRG_511t2:c.185T>C NP_057502.2:p.Phe62Ser
NM_181825.2:c.185T>C NP_861546.1:p.Phe62Ser
NM_181828.2:c.115-2269T>C NP_861966.1:n.115-2269T>C
NM_181829.2:c.185T>C NP_861967.1:p.Phe62Ser
NM_181830.2:c.115-5381T>C NP_861968.1:n.115-5381T>C
NM_181831.2:c.115-5381T>C NP_861969.1:n.115-5381T>C
NM_181832.2:c.185T>C NP_861970.1:p.Phe62Ser
NM_181833.2:c.185T>C NP_861971.1:p.Phe62Ser
NR_156186.1:n.744T>C
XM_017028809.2:c.71T>C XP_016884298.1:p.Phe24Ser
XM_017028810.1:c.71T>C XP_016884299.1:p.Phe24Ser
NM_000268.4:c.185T>C MANE Select NP_000259.1:p.Phe62Ser
NM_181825.3:c.185T>C NP_861546.1:p.Phe62Ser
NM_181828.3:c.115-2269T>C NP_861966.1:n.115-2269T>C
NM_181829.3:c.185T>C NP_861967.1:p.Phe62Ser
NM_181830.3:c.115-5381T>C NP_861968.1:n.115-5381T>C
NM_181831.3:c.115-5381T>C NP_861969.1:n.115-5381T>C
NM_181832.3:c.185T>C NP_861970.1:p.Phe62Ser
NR_156186.2:n.667T>C
NM_181833.3:c.185T>C NP_861971.1:p.Phe62Ser