Canonical Allele Identifier: CA2400693283
Gene: NF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29696897_29696929delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG , CM000684.2:g.29696897_29696929delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG GRCh38
NC_000022.10:g.30092886_30092918delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG , CM000684.1:g.30092886_30092918delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG GRCh37
NC_000022.9:g.28422886_28422918delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NCBI36
NG_009057.1:g.98342_98374delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG , LRG_511:g.98342_98374delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000338641.10:c.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG MANE Select ENSP00000344666.5:n.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAG...
ENST00000672461.1:c.*502-364_*502-332delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG ENSP00000500919.1:n.*502-364_*502-332delinsACCTCCGCCTCCCAGGTA...
ENST00000672896.1:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG ENSP00000500117.1:n.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAG...
ENST00000338641.8:c.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG ENSP00000344666.4:n.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAG...
ENST00000361452.8:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG ENSP00000354897.4:n.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAG...
ENST00000413209.6:c.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG ENSP00000409921.2:n.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAG...
NM_000268.3:c.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG , LRG_511t1:c.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_000259.1:n.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NM_016418.5:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG , LRG_511t2:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_057502.2:n.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NM_181828.2:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_861966.1:n.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NM_181829.2:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_861967.1:n.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NM_181830.2:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_861968.1:n.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NM_181832.2:c.*2170_*2202delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_861970.1:n.*2170_*2202delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NM_181833.2:c.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_861971.1:n.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NR_156186.1:n.4442_4474delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG
XM_017028810.1:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG XP_016884299.1:n.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATT...
NM_000268.4:c.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG MANE Select NP_000259.1:n.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NM_181828.3:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_861966.1:n.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NM_181829.3:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_861967.1:n.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NM_181830.3:c.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_861968.1:n.*2155_*2187delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NM_181832.3:c.*2170_*2202delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_861970.1:n.*2170_*2202delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...
NR_156186.2:n.4365_4397delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG
NM_181833.3:c.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTCCTG NP_861971.1:n.*2095_*2127delinsACCTCCGCCTCCCAGGTACAAGAGATTCTC...