Canonical Allele Identifier: CA658166153

Gene: NF2

Linked Data

• COSMIC: COSN23980397

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695282_29695283insA , CM000684.2:g.29695282_29695283insA	GRCh38
NC_000022.10:g.30091271_30091272insA , CM000684.1:g.30091271_30091272insA	GRCh37
NC_000022.9:g.28421271_28421272insA	NCBI36
NG_009057.1:g.96727_96728insA , LRG_511:g.96727_96728insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*480_*481insA MANE Select	ENSP00000344666.5:n.*480_*481insA
ENST00000672461.1:c.*501+39_*501+40insA	ENSP00000500919.1:n.*501+39_*501+40insA
ENST00000672896.1:c.*540_*541insA	ENSP00000500117.1:n.*540_*541insA
ENST00000338641.8:c.*480_*481insA	ENSP00000344666.4:n.*480_*481insA
ENST00000361452.8:c.*540_*541insA	ENSP00000354897.4:n.*540_*541insA
ENST00000413209.6:c.*480_*481insA	ENSP00000409921.2:n.*480_*481insA
NM_000268.3:c.*480_*481insA , LRG_511t1:c.*480_*481insA	NP_000259.1:n.*480_*481insA
NM_016418.5:c.*540_*541insA , LRG_511t2:c.*540_*541insA	NP_057502.2:n.*540_*541insA
NM_181828.2:c.*540_*541insA	NP_861966.1:n.*540_*541insA
NM_181829.2:c.*540_*541insA	NP_861967.1:n.*540_*541insA
NM_181830.2:c.*540_*541insA	NP_861968.1:n.*540_*541insA
NM_181832.2:c.*555_*556insA	NP_861970.1:n.*555_*556insA
NM_181833.2:c.*480_*481insA	NP_861971.1:n.*480_*481insA
NR_156186.1:n.2827_2828insA
XM_017028810.1:c.*540_*541insA	XP_016884299.1:n.*540_*541insA
NM_000268.4:c.*480_*481insA MANE Select	NP_000259.1:n.*480_*481insA
NM_181828.3:c.*540_*541insA	NP_861966.1:n.*540_*541insA
NM_181829.3:c.*540_*541insA	NP_861967.1:n.*540_*541insA
NM_181830.3:c.*540_*541insA	NP_861968.1:n.*540_*541insA
NM_181832.3:c.*555_*556insA	NP_861970.1:n.*555_*556insA
NR_156186.2:n.2750_2751insA
NM_181833.3:c.*480_*481insA	NP_861971.1:n.*480_*481insA