Canonical Allele Identifier: CA514187675
Gene: NF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.30070841del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29674852del , CM000684.2:g.29674852del GRCh38
NC_000022.10:g.30070841del , CM000684.1:g.30070841del GRCh37
NC_000022.9:g.28400841del NCBI36
NG_009057.1:g.76297del , LRG_511:g.76297del

Transcript Alleles

HGVS Amino-acid change
ENST00000361166.10:c.1222del ENSP00000354529.6:p.Gln408SerfsTer2
ENST00000673312.2:c.*851del ENSP00000500186.2:n.*851del
ENST00000338641.10:c.1357del MANE Select ENSP00000344666.5:p.Gln453SerfsTer2
ENST00000361166.9:c.775del ENSP00000354529.5:p.Gln259SerfsTer2
ENST00000672461.1:c.1357del ENSP00000500919.1:p.Gln453SerfsTer2
ENST00000672805.1:c.*1239del ENSP00000500295.1:n.*1239del
ENST00000672896.1:c.1357del ENSP00000500117.1:p.Gln453SerfsTer2
ENST00000673312.1:c.1376del ENSP00000500186.1:n.1376del
ENST00000334961.11:c.1108del ENSP00000335652.7:p.Gln370SerfsTer2
ENST00000338641.8:c.1357del ENSP00000344666.4:p.Gln453SerfsTer2
ENST00000353887.8:c.1108del ENSP00000340626.4:p.Gln370SerfsTer2
ENST00000361166.8:c.1357del ENSP00000354529.4:p.Gln453SerfsTer2
ENST00000361452.8:c.1234del ENSP00000354897.4:p.Gln412SerfsTer2
ENST00000361676.8:c.1231del ENSP00000355183.4:p.Gln411SerfsTer2
ENST00000397789.3:c.1357del ENSP00000380891.3:p.Gln453SerfsTer2
ENST00000403435.5:c.1270del ENSP00000384029.1:p.Gln424SerfsTer2
ENST00000403999.7:c.1357del ENSP00000384797.3:p.Gln453SerfsTer2
ENST00000413209.6:c.448-19900del ENSP00000409921.2:n.448-19900del
ENST00000432151.5:c.539del ENSP00000395885.1:p.Ser180Ter
NM_000268.3:c.1357del , LRG_511t1:c.1357del NP_000259.1:p.Gln453SerfsTer2
NM_016418.5:c.1357del , LRG_511t2:c.1357del NP_057502.2:p.Gln453SerfsTer2
NM_181825.2:c.1357del NP_861546.1:p.Gln453SerfsTer2
NM_181828.2:c.1231del NP_861966.1:p.Gln411SerfsTer2
NM_181829.2:c.1234del NP_861967.1:p.Gln412SerfsTer2
NM_181830.2:c.1108del NP_861968.1:p.Gln370SerfsTer2
NM_181831.2:c.1108del NP_861969.1:p.Gln370SerfsTer2
NM_181832.2:c.1357del NP_861970.1:p.Gln453SerfsTer2
NM_181833.2:c.448-19900del NP_861971.1:n.448-19900del
NR_156186.1:n.1916del
XM_017028809.2:c.1243del XP_016884298.1:p.Gln415SerfsTer2
XM_017028810.1:c.1243del XP_016884299.1:p.Gln415SerfsTer2
NM_000268.4:c.1357del MANE Select NP_000259.1:p.Gln453SerfsTer2
NM_181825.3:c.1357del NP_861546.1:p.Gln453SerfsTer2
NM_181828.3:c.1231del NP_861966.1:p.Gln411SerfsTer2
NM_181829.3:c.1234del NP_861967.1:p.Gln412SerfsTer2
NM_181830.3:c.1108del NP_861968.1:p.Gln370SerfsTer2
NM_181831.3:c.1108del NP_861969.1:p.Gln370SerfsTer2
NM_181832.3:c.1357del NP_861970.1:p.Gln453SerfsTer2
NR_156186.2:n.1839del
NM_181833.3:c.448-19900del NP_861971.1:n.448-19900del