Canonical Allele Identifier: CA752252086

Gene: NF2

Linked Data

• dbSNP Id: rs1352586293
• gnomAD v3: 22-29697292-G-GC
• gnomAD v4: 22-29697292-G-GC
• MyVariant Identifiers: chr22:g.30093281_30093282insC (hg19) ; chr22:g.29697292_29697293insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29697294dup , CM000684.2:g.29697294dup	GRCh38
NC_000022.10:g.30093283dup , CM000684.1:g.30093283dup	GRCh37
NC_000022.9:g.28423283dup	NCBI36
NG_009057.1:g.98739dup , LRG_511:g.98739dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*2492dup MANE Select	ENSP00000344666.5:n.*2492dup
ENST00000672461.1:c.*535dup	ENSP00000500919.1:n.*535dup
ENST00000672896.1:c.*2552dup	ENSP00000500117.1:n.*2552dup
ENST00000338641.8:c.*2492dup	ENSP00000344666.4:n.*2492dup
ENST00000361452.8:c.*2552dup	ENSP00000354897.4:n.*2552dup
ENST00000413209.6:c.*2492dup	ENSP00000409921.2:n.*2492dup
NM_000268.3:c.*2492dup , LRG_511t1:c.*2492dup	NP_000259.1:n.*2492dup
NM_016418.5:c.*2552dup , LRG_511t2:c.*2552dup	NP_057502.2:n.*2552dup
NM_181828.2:c.*2552dup	NP_861966.1:n.*2552dup
NM_181829.2:c.*2552dup	NP_861967.1:n.*2552dup
NM_181830.2:c.*2552dup	NP_861968.1:n.*2552dup
NM_181832.2:c.*2567dup	NP_861970.1:n.*2567dup
NM_181833.2:c.*2492dup	NP_861971.1:n.*2492dup
NR_156186.1:n.4839dup
XM_017028810.1:c.*2552dup	XP_016884299.1:n.*2552dup
NM_000268.4:c.*2492dup MANE Select	NP_000259.1:n.*2492dup
NM_181828.3:c.*2552dup	NP_861966.1:n.*2552dup
NM_181829.3:c.*2552dup	NP_861967.1:n.*2552dup
NM_181830.3:c.*2552dup	NP_861968.1:n.*2552dup
NM_181832.3:c.*2567dup	NP_861970.1:n.*2567dup
NR_156186.2:n.4762dup
NM_181833.3:c.*2492dup	NP_861971.1:n.*2492dup