Canonical Allele Identifier: CA2577681253

Gene: NF2

Linked Data

• gnomAD v4: 22-29694898-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694903del , CM000684.2:g.29694903del	GRCh38
NC_000022.10:g.30090892del , CM000684.1:g.30090892del	GRCh37
NC_000022.9:g.28420892del	NCBI36
NG_009057.1:g.96348del , LRG_511:g.96348del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*101del	ENSP00000354529.6:n.*101del
ENST00000673312.2:c.*1383del	ENSP00000500186.2:n.*1383del
ENST00000338641.10:c.*101del MANE Select	ENSP00000344666.5:n.*101del
ENST00000361166.9:c.1307del	ENSP00000354529.5:n.1307del
ENST00000672461.1:c.*161del	ENSP00000500919.1:n.*161del
ENST00000672805.1:c.*1771del	ENSP00000500295.1:n.*1771del
ENST00000672896.1:c.*161del	ENSP00000500117.1:n.*161del
ENST00000673312.1:c.1908del	ENSP00000500186.1:n.1908del
ENST00000338641.8:c.*101del	ENSP00000344666.4:n.*101del
ENST00000361452.8:c.*161del	ENSP00000354897.4:n.*161del
ENST00000413209.6:c.*101del	ENSP00000409921.2:n.*101del
ENST00000432151.5:c.*245del	ENSP00000395885.1:n.*245del
NM_000268.3:c.*101del , LRG_511t1:c.*101del	NP_000259.1:n.*101del
NM_016418.5:c.*161del , LRG_511t2:c.*161del	NP_057502.2:n.*161del
NM_181828.2:c.*161del	NP_861966.1:n.*161del
NM_181829.2:c.*161del	NP_861967.1:n.*161del
NM_181830.2:c.*161del	NP_861968.1:n.*161del
NM_181832.2:c.*176del	NP_861970.1:n.*176del
NM_181833.2:c.*101del	NP_861971.1:n.*101del
NR_156186.1:n.2448del
XM_017028809.2:c.*101del	XP_016884298.1:n.*101del
XM_017028810.1:c.*161del	XP_016884299.1:n.*161del
NM_000268.4:c.*101del MANE Select	NP_000259.1:n.*101del
NM_181828.3:c.*161del	NP_861966.1:n.*161del
NM_181829.3:c.*161del	NP_861967.1:n.*161del
NM_181830.3:c.*161del	NP_861968.1:n.*161del
NM_181832.3:c.*176del	NP_861970.1:n.*176del
NR_156186.2:n.2371del
NM_181833.3:c.*101del	NP_861971.1:n.*101del