Canonical Allele Identifier: CA10645249

Gene: NF2

Linked Data

• ClinVar Variation Id: 341086
• ClinVar RCV Id: RCV000307146 ; RCV003221940 ; RCV002488733
• dbSNP Id: rs572307337
• gnomAD v2: 22-30091150-G-A
• gnomAD v3: 22-29695161-G-A
• gnomAD v4: 22-29695161-G-A
• MyVariant Identifiers: chr22:g.30091150G>A (hg19) ; chr22:g.29695161G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695161G>A , CM000684.2:g.29695161G>A	GRCh38
NC_000022.10:g.30091150G>A , CM000684.1:g.30091150G>A	GRCh37
NC_000022.9:g.28421150G>A	NCBI36
NG_009057.1:g.96606G>A , LRG_511:g.96606G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*359G>A MANE Select	ENSP00000344666.5:n.*359G>A
ENST00000672461.1:c.*419G>A	ENSP00000500919.1:n.*419G>A
ENST00000672896.1:c.*419G>A	ENSP00000500117.1:n.*419G>A
ENST00000338641.8:c.*359G>A	ENSP00000344666.4:n.*359G>A
ENST00000361452.8:c.*419G>A	ENSP00000354897.4:n.*419G>A
ENST00000413209.6:c.*359G>A	ENSP00000409921.2:n.*359G>A
NM_000268.3:c.*359G>A , LRG_511t1:c.*359G>A	NP_000259.1:n.*359G>A
NM_016418.5:c.*419G>A , LRG_511t2:c.*419G>A	NP_057502.2:n.*419G>A
NM_181828.2:c.*419G>A	NP_861966.1:n.*419G>A
NM_181829.2:c.*419G>A	NP_861967.1:n.*419G>A
NM_181830.2:c.*419G>A	NP_861968.1:n.*419G>A
NM_181832.2:c.*434G>A	NP_861970.1:n.*434G>A
NM_181833.2:c.*359G>A	NP_861971.1:n.*359G>A
NR_156186.1:n.2706G>A
XM_017028810.1:c.*419G>A	XP_016884299.1:n.*419G>A
NM_000268.4:c.*359G>A MANE Select	NP_000259.1:n.*359G>A
NM_181828.3:c.*419G>A	NP_861966.1:n.*419G>A
NM_181829.3:c.*419G>A	NP_861967.1:n.*419G>A
NM_181830.3:c.*419G>A	NP_861968.1:n.*419G>A
NM_181832.3:c.*434G>A	NP_861970.1:n.*434G>A
NR_156186.2:n.2629G>A
NM_181833.3:c.*359G>A	NP_861971.1:n.*359G>A