Canonical Allele Identifier: CA658166169

Gene: NF2

Linked Data

• COSMIC: COSN22571351

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29696903_29696904insA , CM000684.2:g.29696903_29696904insA	GRCh38
NC_000022.10:g.30092892_30092893insA , CM000684.1:g.30092892_30092893insA	GRCh37
NC_000022.9:g.28422892_28422893insA	NCBI36
NG_009057.1:g.98348_98349insA , LRG_511:g.98348_98349insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*2101_*2102insA MANE Select	ENSP00000344666.5:n.*2101_*2102insA
ENST00000672461.1:c.*502-358_*502-357insA	ENSP00000500919.1:n.*502-358_*502-357insA
ENST00000672896.1:c.*2161_*2162insA	ENSP00000500117.1:n.*2161_*2162insA
ENST00000338641.8:c.*2101_*2102insA	ENSP00000344666.4:n.*2101_*2102insA
ENST00000361452.8:c.*2161_*2162insA	ENSP00000354897.4:n.*2161_*2162insA
ENST00000413209.6:c.*2101_*2102insA	ENSP00000409921.2:n.*2101_*2102insA
NM_000268.3:c.*2101_*2102insA , LRG_511t1:c.*2101_*2102insA	NP_000259.1:n.*2101_*2102insA
NM_016418.5:c.*2161_*2162insA , LRG_511t2:c.*2161_*2162insA	NP_057502.2:n.*2161_*2162insA
NM_181828.2:c.*2161_*2162insA	NP_861966.1:n.*2161_*2162insA
NM_181829.2:c.*2161_*2162insA	NP_861967.1:n.*2161_*2162insA
NM_181830.2:c.*2161_*2162insA	NP_861968.1:n.*2161_*2162insA
NM_181832.2:c.*2176_*2177insA	NP_861970.1:n.*2176_*2177insA
NM_181833.2:c.*2101_*2102insA	NP_861971.1:n.*2101_*2102insA
NR_156186.1:n.4448_4449insA
XM_017028810.1:c.*2161_*2162insA	XP_016884299.1:n.*2161_*2162insA
NM_000268.4:c.*2101_*2102insA MANE Select	NP_000259.1:n.*2101_*2102insA
NM_181828.3:c.*2161_*2162insA	NP_861966.1:n.*2161_*2162insA
NM_181829.3:c.*2161_*2162insA	NP_861967.1:n.*2161_*2162insA
NM_181830.3:c.*2161_*2162insA	NP_861968.1:n.*2161_*2162insA
NM_181832.3:c.*2176_*2177insA	NP_861970.1:n.*2176_*2177insA
NR_156186.2:n.4371_4372insA
NM_181833.3:c.*2101_*2102insA	NP_861971.1:n.*2101_*2102insA