Canonical Allele Identifier: CA2400693967
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29698268_29698269delinsTC , CM000684.2:g.29698268_29698269delinsTC GRCh38
NC_000022.10:g.30094257_30094258delinsTC , CM000684.1:g.30094257_30094258delinsTC GRCh37
NC_000022.9:g.28424257_28424258delinsTC NCBI36
NG_009057.1:g.99713_99714delinsTC , LRG_511:g.99713_99714delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000338641.10:c.*3466_*3467delinsTC MANE Select ENSP00000344666.5:n.*3466_*3467delinsTC
ENST00000672896.1:c.*3526_*3527delinsTC ENSP00000500117.1:n.*3526_*3527delinsTC
ENST00000338641.8:c.*3466_*3467delinsTC ENSP00000344666.4:n.*3466_*3467delinsTC
ENST00000361452.8:c.*3526_*3527delinsTC ENSP00000354897.4:n.*3526_*3527delinsTC
ENST00000413209.6:c.*3466_*3467delinsTC ENSP00000409921.2:n.*3466_*3467delinsTC
NM_000268.3:c.*3466_*3467delinsTC , LRG_511t1:c.*3466_*3467delinsTC NP_000259.1:n.*3466_*3467delinsTC
NM_016418.5:c.*3526_*3527delinsTC , LRG_511t2:c.*3526_*3527delinsTC NP_057502.2:n.*3526_*3527delinsTC
NM_181828.2:c.*3526_*3527delinsTC NP_861966.1:n.*3526_*3527delinsTC
NM_181829.2:c.*3526_*3527delinsTC NP_861967.1:n.*3526_*3527delinsTC
NM_181830.2:c.*3526_*3527delinsTC NP_861968.1:n.*3526_*3527delinsTC
NM_181832.2:c.*3541_*3542delinsTC NP_861970.1:n.*3541_*3542delinsTC
NM_181833.2:c.*3466_*3467delinsTC NP_861971.1:n.*3466_*3467delinsTC
NR_156186.1:n.5813_5814delinsTC
XM_017028810.1:c.*3526_*3527delinsTC XP_016884299.1:n.*3526_*3527delinsTC
NM_000268.4:c.*3466_*3467delinsTC MANE Select NP_000259.1:n.*3466_*3467delinsTC
NM_181828.3:c.*3526_*3527delinsTC NP_861966.1:n.*3526_*3527delinsTC
NM_181829.3:c.*3526_*3527delinsTC NP_861967.1:n.*3526_*3527delinsTC
NM_181830.3:c.*3526_*3527delinsTC NP_861968.1:n.*3526_*3527delinsTC
NM_181832.3:c.*3541_*3542delinsTC NP_861970.1:n.*3541_*3542delinsTC
NR_156186.2:n.5736_5737delinsTC
NM_181833.3:c.*3466_*3467delinsTC NP_861971.1:n.*3466_*3467delinsTC