Canonical Allele Identifier: CA2400693964
Gene: NF2 HGNC NCBI

Linked Data

dbSNP Id: rs2067609196

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29698264_29698266del , CM000684.2:g.29698264_29698266del GRCh38
NC_000022.10:g.30094253_30094255del , CM000684.1:g.30094253_30094255del GRCh37
NC_000022.9:g.28424253_28424255del NCBI36
NG_009057.1:g.99709_99711del , LRG_511:g.99709_99711del

Transcript Alleles

HGVS Amino-acid change
ENST00000338641.10:c.*3462_*3464del MANE Select ENSP00000344666.5:n.*3462_*3464del
ENST00000672896.1:c.*3522_*3524del ENSP00000500117.1:n.*3522_*3524del
ENST00000338641.8:c.*3462_*3464del ENSP00000344666.4:n.*3462_*3464del
ENST00000361452.8:c.*3522_*3524del ENSP00000354897.4:n.*3522_*3524del
ENST00000413209.6:c.*3462_*3464del ENSP00000409921.2:n.*3462_*3464del
NM_000268.3:c.*3462_*3464del , LRG_511t1:c.*3462_*3464del NP_000259.1:n.*3462_*3464del
NM_016418.5:c.*3522_*3524del , LRG_511t2:c.*3522_*3524del NP_057502.2:n.*3522_*3524del
NM_181828.2:c.*3522_*3524del NP_861966.1:n.*3522_*3524del
NM_181829.2:c.*3522_*3524del NP_861967.1:n.*3522_*3524del
NM_181830.2:c.*3522_*3524del NP_861968.1:n.*3522_*3524del
NM_181832.2:c.*3537_*3539del NP_861970.1:n.*3537_*3539del
NM_181833.2:c.*3462_*3464del NP_861971.1:n.*3462_*3464del
NR_156186.1:n.5809_5811del
XM_017028810.1:c.*3522_*3524del XP_016884299.1:n.*3522_*3524del
NM_000268.4:c.*3462_*3464del MANE Select NP_000259.1:n.*3462_*3464del
NM_181828.3:c.*3522_*3524del NP_861966.1:n.*3522_*3524del
NM_181829.3:c.*3522_*3524del NP_861967.1:n.*3522_*3524del
NM_181830.3:c.*3522_*3524del NP_861968.1:n.*3522_*3524del
NM_181832.3:c.*3537_*3539del NP_861970.1:n.*3537_*3539del
NR_156186.2:n.5732_5734del
NM_181833.3:c.*3462_*3464del NP_861971.1:n.*3462_*3464del