Canonical Allele Identifier: CA2400692523

Gene: NF2

Linked Data

• dbSNP Id: rs2067518042

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695265_29695275del , CM000684.2:g.29695265_29695275del	GRCh38
NC_000022.10:g.30091254_30091264del , CM000684.1:g.30091254_30091264del	GRCh37
NC_000022.9:g.28421254_28421264del	NCBI36
NG_009057.1:g.96710_96720del , LRG_511:g.96710_96720del

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*463_*473del MANE Select	ENSP00000344666.5:n.*463_*473del
ENST00000672461.1:c.*501+22_*501+32del	ENSP00000500919.1:n.*501+22_*501+32del
ENST00000672896.1:c.*523_*533del	ENSP00000500117.1:n.*523_*533del
ENST00000338641.8:c.*463_*473del	ENSP00000344666.4:n.*463_*473del
ENST00000361452.8:c.*523_*533del	ENSP00000354897.4:n.*523_*533del
ENST00000413209.6:c.*463_*473del	ENSP00000409921.2:n.*463_*473del
NM_000268.3:c.*463_*473del , LRG_511t1:c.*463_*473del	NP_000259.1:n.*463_*473del
NM_016418.5:c.*523_*533del , LRG_511t2:c.*523_*533del	NP_057502.2:n.*523_*533del
NM_181828.2:c.*523_*533del	NP_861966.1:n.*523_*533del
NM_181829.2:c.*523_*533del	NP_861967.1:n.*523_*533del
NM_181830.2:c.*523_*533del	NP_861968.1:n.*523_*533del
NM_181832.2:c.*538_*548del	NP_861970.1:n.*538_*548del
NM_181833.2:c.*463_*473del	NP_861971.1:n.*463_*473del
NR_156186.1:n.2810_2820del
XM_017028810.1:c.*523_*533del	XP_016884299.1:n.*523_*533del
NM_000268.4:c.*463_*473del MANE Select	NP_000259.1:n.*463_*473del
NM_181828.3:c.*523_*533del	NP_861966.1:n.*523_*533del
NM_181829.3:c.*523_*533del	NP_861967.1:n.*523_*533del
NM_181830.3:c.*523_*533del	NP_861968.1:n.*523_*533del
NM_181832.3:c.*538_*548del	NP_861970.1:n.*538_*548del
NR_156186.2:n.2733_2743del
NM_181833.3:c.*463_*473del	NP_861971.1:n.*463_*473del