Canonical Allele Identifier: CA1024928241
Gene: NF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29696816_29696825del , CM000684.2:g.29696816_29696825del GRCh38
NC_000022.10:g.30092805_30092814del , CM000684.1:g.30092805_30092814del GRCh37
NC_000022.9:g.28422805_28422814del NCBI36
NG_009057.1:g.98261_98270del , LRG_511:g.98261_98270del

Transcript Alleles

HGVS Amino-acid change
ENST00000338641.10:c.*2014_*2023del MANE Select ENSP00000344666.5:n.*2014_*2023del
ENST00000672461.1:c.*502-445_*502-436del ENSP00000500919.1:n.*502-445_*502-436del
ENST00000672896.1:c.*2074_*2083del ENSP00000500117.1:n.*2074_*2083del
ENST00000338641.8:c.*2014_*2023del ENSP00000344666.4:n.*2014_*2023del
ENST00000361452.8:c.*2074_*2083del ENSP00000354897.4:n.*2074_*2083del
ENST00000413209.6:c.*2014_*2023del ENSP00000409921.2:n.*2014_*2023del
NM_000268.3:c.*2014_*2023del , LRG_511t1:c.*2014_*2023del NP_000259.1:n.*2014_*2023del
NM_016418.5:c.*2074_*2083del , LRG_511t2:c.*2074_*2083del NP_057502.2:n.*2074_*2083del
NM_181828.2:c.*2074_*2083del NP_861966.1:n.*2074_*2083del
NM_181829.2:c.*2074_*2083del NP_861967.1:n.*2074_*2083del
NM_181830.2:c.*2074_*2083del NP_861968.1:n.*2074_*2083del
NM_181832.2:c.*2089_*2098del NP_861970.1:n.*2089_*2098del
NM_181833.2:c.*2014_*2023del NP_861971.1:n.*2014_*2023del
NR_156186.1:n.4361_4370del
XM_017028810.1:c.*2074_*2083del XP_016884299.1:n.*2074_*2083del
NM_000268.4:c.*2014_*2023del MANE Select NP_000259.1:n.*2014_*2023del
NM_181828.3:c.*2074_*2083del NP_861966.1:n.*2074_*2083del
NM_181829.3:c.*2074_*2083del NP_861967.1:n.*2074_*2083del
NM_181830.3:c.*2074_*2083del NP_861968.1:n.*2074_*2083del
NM_181832.3:c.*2089_*2098del NP_861970.1:n.*2089_*2098del
NR_156186.2:n.4284_4293del
NM_181833.3:c.*2014_*2023del NP_861971.1:n.*2014_*2023del