Canonical Allele Identifier: CA2400693588

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29697523_29697524delinsCT , CM000684.2:g.29697523_29697524delinsCT	GRCh38
NC_000022.10:g.30093512_30093513delinsCT , CM000684.1:g.30093512_30093513delinsCT	GRCh37
NC_000022.9:g.28423512_28423513delinsCT	NCBI36
NG_009057.1:g.98968_98969delinsCT , LRG_511:g.98968_98969delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*2721_*2722delinsCT MANE Select	ENSP00000344666.5:n.*2721_*2722delinsCT
ENST00000672461.1:c.*764_*765delinsCT	ENSP00000500919.1:n.*764_*765delinsCT
ENST00000672896.1:c.*2781_*2782delinsCT	ENSP00000500117.1:n.*2781_*2782delinsCT
ENST00000338641.8:c.*2721_*2722delinsCT	ENSP00000344666.4:n.*2721_*2722delinsCT
ENST00000361452.8:c.*2781_*2782delinsCT	ENSP00000354897.4:n.*2781_*2782delinsCT
ENST00000413209.6:c.*2721_*2722delinsCT	ENSP00000409921.2:n.*2721_*2722delinsCT
NM_000268.3:c.*2721_*2722delinsCT , LRG_511t1:c.*2721_*2722delinsCT	NP_000259.1:n.*2721_*2722delinsCT
NM_016418.5:c.*2781_*2782delinsCT , LRG_511t2:c.*2781_*2782delinsCT	NP_057502.2:n.*2781_*2782delinsCT
NM_181828.2:c.*2781_*2782delinsCT	NP_861966.1:n.*2781_*2782delinsCT
NM_181829.2:c.*2781_*2782delinsCT	NP_861967.1:n.*2781_*2782delinsCT
NM_181830.2:c.*2781_*2782delinsCT	NP_861968.1:n.*2781_*2782delinsCT
NM_181832.2:c.*2796_*2797delinsCT	NP_861970.1:n.*2796_*2797delinsCT
NM_181833.2:c.*2721_*2722delinsCT	NP_861971.1:n.*2721_*2722delinsCT
NR_156186.1:n.5068_5069delinsCT
XM_017028810.1:c.*2781_*2782delinsCT	XP_016884299.1:n.*2781_*2782delinsCT
NM_000268.4:c.*2721_*2722delinsCT MANE Select	NP_000259.1:n.*2721_*2722delinsCT
NM_181828.3:c.*2781_*2782delinsCT	NP_861966.1:n.*2781_*2782delinsCT
NM_181829.3:c.*2781_*2782delinsCT	NP_861967.1:n.*2781_*2782delinsCT
NM_181830.3:c.*2781_*2782delinsCT	NP_861968.1:n.*2781_*2782delinsCT
NM_181832.3:c.*2796_*2797delinsCT	NP_861970.1:n.*2796_*2797delinsCT
NR_156186.2:n.4991_4992delinsCT
NM_181833.3:c.*2721_*2722delinsCT	NP_861971.1:n.*2721_*2722delinsCT