Canonical Allele Identifier: CA2656033455

Gene: NF2

Linked Data

• gnomAD v4: 22-29695229-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695229T>G , CM000684.2:g.29695229T>G	GRCh38
NC_000022.10:g.30091218T>G , CM000684.1:g.30091218T>G	GRCh37
NC_000022.9:g.28421218T>G	NCBI36
NG_009057.1:g.96674T>G , LRG_511:g.96674T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*427T>G MANE Select	ENSP00000344666.5:n.*427T>G
ENST00000672461.1:c.*487T>G	ENSP00000500919.1:n.*487T>G
ENST00000672896.1:c.*487T>G	ENSP00000500117.1:n.*487T>G
ENST00000338641.8:c.*427T>G	ENSP00000344666.4:n.*427T>G
ENST00000361452.8:c.*487T>G	ENSP00000354897.4:n.*487T>G
ENST00000413209.6:c.*427T>G	ENSP00000409921.2:n.*427T>G
NM_000268.3:c.*427T>G , LRG_511t1:c.*427T>G	NP_000259.1:n.*427T>G
NM_016418.5:c.*487T>G , LRG_511t2:c.*487T>G	NP_057502.2:n.*487T>G
NM_181828.2:c.*487T>G	NP_861966.1:n.*487T>G
NM_181829.2:c.*487T>G	NP_861967.1:n.*487T>G
NM_181830.2:c.*487T>G	NP_861968.1:n.*487T>G
NM_181832.2:c.*502T>G	NP_861970.1:n.*502T>G
NM_181833.2:c.*427T>G	NP_861971.1:n.*427T>G
NR_156186.1:n.2774T>G
XM_017028810.1:c.*487T>G	XP_016884299.1:n.*487T>G
NM_000268.4:c.*427T>G MANE Select	NP_000259.1:n.*427T>G
NM_181828.3:c.*487T>G	NP_861966.1:n.*487T>G
NM_181829.3:c.*487T>G	NP_861967.1:n.*487T>G
NM_181830.3:c.*487T>G	NP_861968.1:n.*487T>G
NM_181832.3:c.*502T>G	NP_861970.1:n.*502T>G
NR_156186.2:n.2697T>G
NM_181833.3:c.*427T>G	NP_861971.1:n.*427T>G