Canonical Allele Identifier: CA2400693712

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29697760_29697762delinsTTC , CM000684.2:g.29697760_29697762delinsTTC	GRCh38
NC_000022.10:g.30093749_30093751delinsTTC , CM000684.1:g.30093749_30093751delinsTTC	GRCh37
NC_000022.9:g.28423749_28423751delinsTTC	NCBI36
NG_009057.1:g.99205_99207delinsTTC , LRG_511:g.99205_99207delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*2958_*2960delinsTTC MANE Select	ENSP00000344666.5:n.*2958_*2960delinsTTC
ENST00000672896.1:c.*3018_*3020delinsTTC	ENSP00000500117.1:n.*3018_*3020delinsTTC
ENST00000338641.8:c.*2958_*2960delinsTTC	ENSP00000344666.4:n.*2958_*2960delinsTTC
ENST00000361452.8:c.*3018_*3020delinsTTC	ENSP00000354897.4:n.*3018_*3020delinsTTC
ENST00000413209.6:c.*2958_*2960delinsTTC	ENSP00000409921.2:n.*2958_*2960delinsTTC
NM_000268.3:c.*2958_*2960delinsTTC , LRG_511t1:c.*2958_*2960delinsTTC	NP_000259.1:n.*2958_*2960delinsTTC
NM_016418.5:c.*3018_*3020delinsTTC , LRG_511t2:c.*3018_*3020delinsTTC	NP_057502.2:n.*3018_*3020delinsTTC
NM_181828.2:c.*3018_*3020delinsTTC	NP_861966.1:n.*3018_*3020delinsTTC
NM_181829.2:c.*3018_*3020delinsTTC	NP_861967.1:n.*3018_*3020delinsTTC
NM_181830.2:c.*3018_*3020delinsTTC	NP_861968.1:n.*3018_*3020delinsTTC
NM_181832.2:c.*3033_*3035delinsTTC	NP_861970.1:n.*3033_*3035delinsTTC
NM_181833.2:c.*2958_*2960delinsTTC	NP_861971.1:n.*2958_*2960delinsTTC
NR_156186.1:n.5305_5307delinsTTC
XM_017028810.1:c.*3018_*3020delinsTTC	XP_016884299.1:n.*3018_*3020delinsTTC
NM_000268.4:c.*2958_*2960delinsTTC MANE Select	NP_000259.1:n.*2958_*2960delinsTTC
NM_181828.3:c.*3018_*3020delinsTTC	NP_861966.1:n.*3018_*3020delinsTTC
NM_181829.3:c.*3018_*3020delinsTTC	NP_861967.1:n.*3018_*3020delinsTTC
NM_181830.3:c.*3018_*3020delinsTTC	NP_861968.1:n.*3018_*3020delinsTTC
NM_181832.3:c.*3033_*3035delinsTTC	NP_861970.1:n.*3033_*3035delinsTTC
NR_156186.2:n.5228_5230delinsTTC
NM_181833.3:c.*2958_*2960delinsTTC	NP_861971.1:n.*2958_*2960delinsTTC