Canonical Allele Identifier: CA2400685401
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29678217C= , CM000684.2:g.29678217C= GRCh38
NC_000022.10:g.30074206C= , CM000684.1:g.30074206C= GRCh37
NC_000022.9:g.28404206C= NCBI36
NG_009057.1:g.79662C= , LRG_511:g.79662C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361166.10:c.1333C= ENSP00000354529.6:p.Pro445=
ENST00000673312.2:c.*962C= ENSP00000500186.2:n.*962C=
ENST00000338641.10:c.1468C= MANE Select ENSP00000344666.5:p.Pro490=
ENST00000361166.9:c.886C= ENSP00000354529.5:p.Pro296=
ENST00000672461.1:c.1468C= ENSP00000500919.1:p.Pro490=
ENST00000672805.1:c.*1350C= ENSP00000500295.1:n.*1350C=
ENST00000672896.1:c.1468C= ENSP00000500117.1:p.Pro490=
ENST00000673312.1:c.1487C= ENSP00000500186.1:n.1487C=
ENST00000334961.11:c.1219C= ENSP00000335652.7:p.Pro407=
ENST00000338641.8:c.1468C= ENSP00000344666.4:p.Pro490=
ENST00000353887.8:c.1219C= ENSP00000340626.4:p.Pro407=
ENST00000361166.8:c.1468C= ENSP00000354529.4:p.Pro490=
ENST00000361452.8:c.1345C= ENSP00000354897.4:p.Pro449=
ENST00000361676.8:c.1342C= ENSP00000355183.4:p.Pro448=
ENST00000397789.3:c.1468C= ENSP00000380891.3:p.Pro490=
ENST00000403435.5:c.1381C= ENSP00000384029.1:p.Pro461=
ENST00000403999.7:c.1468C= ENSP00000384797.3:p.Pro490=
ENST00000413209.6:c.448-16535C= ENSP00000409921.2:n.448-16535C=
ENST00000432151.5:c.650C= ENSP00000395885.1:p.Thr217=
NM_000268.3:c.1468C= , LRG_511t1:c.1468C= NP_000259.1:p.Pro490=
NM_016418.5:c.1468C= , LRG_511t2:c.1468C= NP_057502.2:p.Pro490=
NM_181825.2:c.1468C= NP_861546.1:p.Pro490=
NM_181828.2:c.1342C= NP_861966.1:p.Pro448=
NM_181829.2:c.1345C= NP_861967.1:p.Pro449=
NM_181830.2:c.1219C= NP_861968.1:p.Pro407=
NM_181831.2:c.1219C= NP_861969.1:p.Pro407=
NM_181832.2:c.1468C= NP_861970.1:p.Pro490=
NM_181833.2:c.448-16535C= NP_861971.1:n.448-16535C=
NR_156186.1:n.2027C=
XM_017028809.2:c.1354C= XP_016884298.1:p.Pro452=
XM_017028810.1:c.1354C= XP_016884299.1:p.Pro452=
NM_000268.4:c.1468C= MANE Select NP_000259.1:p.Pro490=
NM_181825.3:c.1468C= NP_861546.1:p.Pro490=
NM_181828.3:c.1342C= NP_861966.1:p.Pro448=
NM_181829.3:c.1345C= NP_861967.1:p.Pro449=
NM_181830.3:c.1219C= NP_861968.1:p.Pro407=
NM_181831.3:c.1219C= NP_861969.1:p.Pro407=
NM_181832.3:c.1468C= NP_861970.1:p.Pro490=
NR_156186.2:n.1950C=
NM_181833.3:c.448-16535C= NP_861971.1:n.448-16535C=