Canonical Allele Identifier: CA891843608
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 568174
ClinVar RCV Id: RCV000688441
dbSNP Id: rs1569297926

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29661339_29661341dup , CM000684.2:g.29661339_29661341dup GRCh38
NC_000022.10:g.30057328_30057330dup , CM000684.1:g.30057328_30057330dup GRCh37
NC_000022.9:g.28387328_28387330dup NCBI36
NG_009057.1:g.62784_62786dup , LRG_511:g.62784_62786dup

Transcript Alleles

HGVS Amino-acid change
ENST00000361166.10:c.675+3075_675+3077dup ENSP00000354529.6:n.675+3075_675+3077dup
ENST00000673312.2:c.*304_*304+2dup
ENST00000338641.10:c.810_810+2dup
ENST00000361166.9:c.228+3075_228+3077dup ENSP00000354529.5:n.228+3075_228+3077dup
ENST00000672461.1:c.810_810+2dup
ENST00000672805.1:c.*692_*692+2dup
ENST00000672896.1:c.810_810+2dup
ENST00000673312.1:c.829_829+2dup
ENST00000334961.11:c.561_561+2dup
ENST00000338641.8:c.810_810+2dup
ENST00000353887.8:c.561_561+2dup
ENST00000361166.8:c.810_810+2dup
ENST00000361452.8:c.687_687+2dup
ENST00000361676.8:c.684_684+2dup
ENST00000397789.3:c.810_810+2dup
ENST00000403435.5:c.810_810+2dup
ENST00000403999.7:c.810_810+2dup
ENST00000413209.6:c.447+19054_447+19056dup ENSP00000409921.2:n.447+19054_447+19056du...
ENST00000432151.5:c.333_333+2dup
NM_000268.3:c.810_810+2dup , LRG_511t1:c.810_810+2dup
NM_016418.5:c.810_810+2dup , LRG_511t2:c.810_810+2dup
NM_181825.2:c.810_810+2dup
NM_181828.2:c.684_684+2dup
NM_181829.2:c.687_687+2dup
NM_181830.2:c.561_561+2dup
NM_181831.2:c.561_561+2dup
NM_181832.2:c.810_810+2dup
NM_181833.2:c.447+19054_447+19056dup NP_861971.1:n.447+19054_447+19056dup
NR_156186.1:n.1369_1369+2dup
XM_017028809.2:c.696_696+2dup
XM_017028810.1:c.696_696+2dup
NM_000268.4:c.810_810+2dup
NM_181825.3:c.810_810+2dup
NM_181828.3:c.684_684+2dup
NM_181829.3:c.687_687+2dup
NM_181830.3:c.561_561+2dup
NM_181831.3:c.561_561+2dup
NM_181832.3:c.810_810+2dup
NR_156186.2:n.1292_1292+2dup
NM_181833.3:c.447+19054_447+19056dup NP_861971.1:n.447+19054_447+19056dup