Canonical Allele Identifier: CA411143661
Gene: NF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29661208A>C , CM000684.2:g.29661208A>C GRCh38
NC_000022.10:g.30057197A>C , CM000684.1:g.30057197A>C GRCh37
NC_000022.9:g.28387197A>C NCBI36
NG_009057.1:g.62653A>C , LRG_511:g.62653A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.675+2944A>C ENSP00000354529.6:n.675+2944A>C
ENST00000673312.2:c.*173A>C ENSP00000500186.2:n.*173A>C
ENST00000338641.10:c.679A>C MANE Select ENSP00000344666.5:p.Lys227Gln
ENST00000361166.9:c.228+2944A>C ENSP00000354529.5:n.228+2944A>C
ENST00000672461.1:c.679A>C ENSP00000500919.1:p.Lys227Gln
ENST00000672805.1:c.*561A>C ENSP00000500295.1:n.*561A>C
ENST00000672896.1:c.679A>C ENSP00000500117.1:p.Lys227Gln
ENST00000673312.1:c.698A>C ENSP00000500186.1:n.698A>C
ENST00000334961.11:c.430A>C ENSP00000335652.7:p.Lys144Gln
ENST00000338641.8:c.679A>C ENSP00000344666.4:p.Lys227Gln
ENST00000353887.8:c.430A>C ENSP00000340626.4:p.Lys144Gln
ENST00000361166.8:c.679A>C ENSP00000354529.4:p.Lys227Gln
ENST00000361452.8:c.556A>C ENSP00000354897.4:p.Lys186Gln
ENST00000361676.8:c.553A>C ENSP00000355183.4:p.Lys185Gln
ENST00000397789.3:c.679A>C ENSP00000380891.3:p.Lys227Gln
ENST00000403435.5:c.679A>C ENSP00000384029.1:p.Lys227Gln
ENST00000403999.7:c.679A>C ENSP00000384797.3:p.Lys227Gln
ENST00000413209.6:c.447+18923A>C ENSP00000409921.2:n.447+18923A>C
ENST00000432151.5:c.202A>C ENSP00000395885.1:p.Lys68Gln
NM_000268.3:c.679A>C , LRG_511t1:c.679A>C NP_000259.1:p.Lys227Gln
NM_016418.5:c.679A>C , LRG_511t2:c.679A>C NP_057502.2:p.Lys227Gln
NM_181825.2:c.679A>C NP_861546.1:p.Lys227Gln
NM_181828.2:c.553A>C NP_861966.1:p.Lys185Gln
NM_181829.2:c.556A>C NP_861967.1:p.Lys186Gln
NM_181830.2:c.430A>C NP_861968.1:p.Lys144Gln
NM_181831.2:c.430A>C NP_861969.1:p.Lys144Gln
NM_181832.2:c.679A>C NP_861970.1:p.Lys227Gln
NM_181833.2:c.447+18923A>C NP_861971.1:n.447+18923A>C
NR_156186.1:n.1238A>C
XM_017028809.2:c.565A>C XP_016884298.1:p.Lys189Gln
XM_017028810.1:c.565A>C XP_016884299.1:p.Lys189Gln
NM_000268.4:c.679A>C MANE Select NP_000259.1:p.Lys227Gln
NM_181825.3:c.679A>C NP_861546.1:p.Lys227Gln
NM_181828.3:c.553A>C NP_861966.1:p.Lys185Gln
NM_181829.3:c.556A>C NP_861967.1:p.Lys186Gln
NM_181830.3:c.430A>C NP_861968.1:p.Lys144Gln
NM_181831.3:c.430A>C NP_861969.1:p.Lys144Gln
NM_181832.3:c.679A>C NP_861970.1:p.Lys227Gln
NR_156186.2:n.1161A>C
NM_181833.3:c.447+18923A>C NP_861971.1:n.447+18923A>C