Canonical Allele Identifier: CA2400692403
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29695006C= , CM000684.2:g.29695006C= GRCh38
NC_000022.10:g.30090995C= , CM000684.1:g.30090995C= GRCh37
NC_000022.9:g.28420995C= NCBI36
NG_009057.1:g.96451C= , LRG_511:g.96451C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361166.10:c.*204C= ENSP00000354529.6:n.*204C=
ENST00000673312.2:c.*1486C= ENSP00000500186.2:n.*1486C=
ENST00000338641.10:c.*204C= MANE Select ENSP00000344666.5:n.*204C=
ENST00000361166.9:c.1410C= ENSP00000354529.5:n.1410C=
ENST00000672461.1:c.*264C= ENSP00000500919.1:n.*264C=
ENST00000672896.1:c.*264C= ENSP00000500117.1:n.*264C=
ENST00000673312.1:c.2011C= ENSP00000500186.1:n.2011C=
ENST00000338641.8:c.*204C= ENSP00000344666.4:n.*204C=
ENST00000361452.8:c.*264C= ENSP00000354897.4:n.*264C=
ENST00000413209.6:c.*204C= ENSP00000409921.2:n.*204C=
NM_000268.3:c.*204C= , LRG_511t1:c.*204C= NP_000259.1:n.*204C=
NM_016418.5:c.*264C= , LRG_511t2:c.*264C= NP_057502.2:n.*264C=
NM_181828.2:c.*264C= NP_861966.1:n.*264C=
NM_181829.2:c.*264C= NP_861967.1:n.*264C=
NM_181830.2:c.*264C= NP_861968.1:n.*264C=
NM_181832.2:c.*279C= NP_861970.1:n.*279C=
NM_181833.2:c.*204C= NP_861971.1:n.*204C=
NR_156186.1:n.2551C=
XM_017028809.2:c.*204C= XP_016884298.1:n.*204C=
XM_017028810.1:c.*264C= XP_016884299.1:n.*264C=
NM_000268.4:c.*204C= MANE Select NP_000259.1:n.*204C=
NM_181828.3:c.*264C= NP_861966.1:n.*264C=
NM_181829.3:c.*264C= NP_861967.1:n.*264C=
NM_181830.3:c.*264C= NP_861968.1:n.*264C=
NM_181832.3:c.*279C= NP_861970.1:n.*279C=
NR_156186.2:n.2474C=
NM_181833.3:c.*204C= NP_861971.1:n.*204C=