Canonical Allele Identifier: CA2400693290

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29696906_29696908delinsTCC , CM000684.2:g.29696906_29696908delinsTCC	GRCh38
NC_000022.10:g.30092895_30092897delinsTCC , CM000684.1:g.30092895_30092897delinsTCC	GRCh37
NC_000022.9:g.28422895_28422897delinsTCC	NCBI36
NG_009057.1:g.98351_98353delinsTCC , LRG_511:g.98351_98353delinsTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*2104_*2106delinsTCC MANE Select	ENSP00000344666.5:n.*2104_*2106delinsTCC
ENST00000672461.1:c.*502-355_*502-353delinsTCC	ENSP00000500919.1:n.*502-355_*502-353deli...
ENST00000672896.1:c.*2164_*2166delinsTCC	ENSP00000500117.1:n.*2164_*2166delinsTCC
ENST00000338641.8:c.*2104_*2106delinsTCC	ENSP00000344666.4:n.*2104_*2106delinsTCC
ENST00000361452.8:c.*2164_*2166delinsTCC	ENSP00000354897.4:n.*2164_*2166delinsTCC
ENST00000413209.6:c.*2104_*2106delinsTCC	ENSP00000409921.2:n.*2104_*2106delinsTCC
NM_000268.3:c.*2104_*2106delinsTCC , LRG_511t1:c.*2104_*2106delinsTCC	NP_000259.1:n.*2104_*2106delinsTCC
NM_016418.5:c.*2164_*2166delinsTCC , LRG_511t2:c.*2164_*2166delinsTCC	NP_057502.2:n.*2164_*2166delinsTCC
NM_181828.2:c.*2164_*2166delinsTCC	NP_861966.1:n.*2164_*2166delinsTCC
NM_181829.2:c.*2164_*2166delinsTCC	NP_861967.1:n.*2164_*2166delinsTCC
NM_181830.2:c.*2164_*2166delinsTCC	NP_861968.1:n.*2164_*2166delinsTCC
NM_181832.2:c.*2179_*2181delinsTCC	NP_861970.1:n.*2179_*2181delinsTCC
NM_181833.2:c.*2104_*2106delinsTCC	NP_861971.1:n.*2104_*2106delinsTCC
NR_156186.1:n.4451_4453delinsTCC
XM_017028810.1:c.*2164_*2166delinsTCC	XP_016884299.1:n.*2164_*2166delinsTCC
NM_000268.4:c.*2104_*2106delinsTCC MANE Select	NP_000259.1:n.*2104_*2106delinsTCC
NM_181828.3:c.*2164_*2166delinsTCC	NP_861966.1:n.*2164_*2166delinsTCC
NM_181829.3:c.*2164_*2166delinsTCC	NP_861967.1:n.*2164_*2166delinsTCC
NM_181830.3:c.*2164_*2166delinsTCC	NP_861968.1:n.*2164_*2166delinsTCC
NM_181832.3:c.*2179_*2181delinsTCC	NP_861970.1:n.*2179_*2181delinsTCC
NR_156186.2:n.4374_4376delinsTCC
NM_181833.3:c.*2104_*2106delinsTCC	NP_861971.1:n.*2104_*2106delinsTCC