Canonical Allele Identifier: CA2656033676

Gene: NF2

Linked Data

• gnomAD v4: 22-29695338-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695339del , CM000684.2:g.29695339del	GRCh38
NC_000022.10:g.30091328del , CM000684.1:g.30091328del	GRCh37
NC_000022.9:g.28421328del	NCBI36
NG_009057.1:g.96784del , LRG_511:g.96784del

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*537del MANE Select	ENSP00000344666.5:n.*537del
ENST00000672461.1:c.*501+96del	ENSP00000500919.1:n.*501+96del
ENST00000672896.1:c.*597del	ENSP00000500117.1:n.*597del
ENST00000338641.8:c.*537del	ENSP00000344666.4:n.*537del
ENST00000361452.8:c.*597del	ENSP00000354897.4:n.*597del
ENST00000413209.6:c.*537del	ENSP00000409921.2:n.*537del
NM_000268.3:c.*537del , LRG_511t1:c.*537del	NP_000259.1:n.*537del
NM_016418.5:c.*597del , LRG_511t2:c.*597del	NP_057502.2:n.*597del
NM_181828.2:c.*597del	NP_861966.1:n.*597del
NM_181829.2:c.*597del	NP_861967.1:n.*597del
NM_181830.2:c.*597del	NP_861968.1:n.*597del
NM_181832.2:c.*612del	NP_861970.1:n.*612del
NM_181833.2:c.*537del	NP_861971.1:n.*537del
NR_156186.1:n.2884del
XM_017028810.1:c.*597del	XP_016884299.1:n.*597del
NM_000268.4:c.*537del MANE Select	NP_000259.1:n.*537del
NM_181828.3:c.*597del	NP_861966.1:n.*597del
NM_181829.3:c.*597del	NP_861967.1:n.*597del
NM_181830.3:c.*597del	NP_861968.1:n.*597del
NM_181832.3:c.*612del	NP_861970.1:n.*612del
NR_156186.2:n.2807del
NM_181833.3:c.*537del	NP_861971.1:n.*537del