Canonical Allele Identifier: CA2656036147
Gene: NF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29696965_29696971del , CM000684.2:g.29696965_29696971del GRCh38
NC_000022.10:g.30092954_30092960del , CM000684.1:g.30092954_30092960del GRCh37
NC_000022.9:g.28422954_28422960del NCBI36
NG_009057.1:g.98410_98416del , LRG_511:g.98410_98416del

Transcript Alleles

HGVS Amino-acid change
ENST00000338641.10:c.*2163_*2169del MANE Select ENSP00000344666.5:n.*2163_*2169del
ENST00000672461.1:c.*502-296_*502-290del ENSP00000500919.1:n.*502-296_*502-290del
ENST00000672896.1:c.*2223_*2229del ENSP00000500117.1:n.*2223_*2229del
ENST00000338641.8:c.*2163_*2169del ENSP00000344666.4:n.*2163_*2169del
ENST00000361452.8:c.*2223_*2229del ENSP00000354897.4:n.*2223_*2229del
ENST00000413209.6:c.*2163_*2169del ENSP00000409921.2:n.*2163_*2169del
NM_000268.3:c.*2163_*2169del , LRG_511t1:c.*2163_*2169del NP_000259.1:n.*2163_*2169del
NM_016418.5:c.*2223_*2229del , LRG_511t2:c.*2223_*2229del NP_057502.2:n.*2223_*2229del
NM_181828.2:c.*2223_*2229del NP_861966.1:n.*2223_*2229del
NM_181829.2:c.*2223_*2229del NP_861967.1:n.*2223_*2229del
NM_181830.2:c.*2223_*2229del NP_861968.1:n.*2223_*2229del
NM_181832.2:c.*2238_*2244del NP_861970.1:n.*2238_*2244del
NM_181833.2:c.*2163_*2169del NP_861971.1:n.*2163_*2169del
NR_156186.1:n.4510_4516del
XM_017028810.1:c.*2223_*2229del XP_016884299.1:n.*2223_*2229del
NM_000268.4:c.*2163_*2169del MANE Select NP_000259.1:n.*2163_*2169del
NM_181828.3:c.*2223_*2229del NP_861966.1:n.*2223_*2229del
NM_181829.3:c.*2223_*2229del NP_861967.1:n.*2223_*2229del
NM_181830.3:c.*2223_*2229del NP_861968.1:n.*2223_*2229del
NM_181832.3:c.*2238_*2244del NP_861970.1:n.*2238_*2244del
NR_156186.2:n.4433_4439del
NM_181833.3:c.*2163_*2169del NP_861971.1:n.*2163_*2169del