Canonical Allele Identifier: CA10651013

Gene: NF2

Linked Data

• ClinVar Variation Id: 341111
• ClinVar RCV Id: RCV000274715
• dbSNP Id: rs376061969
• gnomAD v2: 22-30092229-A-G
• gnomAD v3: 22-29696240-A-G
• gnomAD v4: 22-29696240-A-G
• MyVariant Identifiers: chr22:g.30092229A>G (hg19) ; chr22:g.29696240A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29696240A>G , CM000684.2:g.29696240A>G	GRCh38
NC_000022.10:g.30092229A>G , CM000684.1:g.30092229A>G	GRCh37
NC_000022.9:g.28422229A>G	NCBI36
NG_009057.1:g.97685A>G , LRG_511:g.97685A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*1438A>G MANE Select	ENSP00000344666.5:n.*1438A>G
ENST00000672461.1:c.*501+997A>G	ENSP00000500919.1:n.*501+997A>G
ENST00000672896.1:c.*1498A>G	ENSP00000500117.1:n.*1498A>G
ENST00000338641.8:c.*1438A>G	ENSP00000344666.4:n.*1438A>G
ENST00000361452.8:c.*1498A>G	ENSP00000354897.4:n.*1498A>G
ENST00000413209.6:c.*1438A>G	ENSP00000409921.2:n.*1438A>G
NM_000268.3:c.*1438A>G , LRG_511t1:c.*1438A>G	NP_000259.1:n.*1438A>G
NM_016418.5:c.*1498A>G , LRG_511t2:c.*1498A>G	NP_057502.2:n.*1498A>G
NM_181828.2:c.*1498A>G	NP_861966.1:n.*1498A>G
NM_181829.2:c.*1498A>G	NP_861967.1:n.*1498A>G
NM_181830.2:c.*1498A>G	NP_861968.1:n.*1498A>G
NM_181832.2:c.*1513A>G	NP_861970.1:n.*1513A>G
NM_181833.2:c.*1438A>G	NP_861971.1:n.*1438A>G
NR_156186.1:n.3785A>G
XM_017028810.1:c.*1498A>G	XP_016884299.1:n.*1498A>G
NM_000268.4:c.*1438A>G MANE Select	NP_000259.1:n.*1438A>G
NM_181828.3:c.*1498A>G	NP_861966.1:n.*1498A>G
NM_181829.3:c.*1498A>G	NP_861967.1:n.*1498A>G
NM_181830.3:c.*1498A>G	NP_861968.1:n.*1498A>G
NM_181832.3:c.*1513A>G	NP_861970.1:n.*1513A>G
NR_156186.2:n.3708A>G
NM_181833.3:c.*1438A>G	NP_861971.1:n.*1438A>G