Canonical Allele Identifier: CA2656033067

Gene: NF2

Linked Data

• gnomAD v4: 22-29694945-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694948del , CM000684.2:g.29694948del	GRCh38
NC_000022.10:g.30090937del , CM000684.1:g.30090937del	GRCh37
NC_000022.9:g.28420937del	NCBI36
NG_009057.1:g.96393del , LRG_511:g.96393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*146del	ENSP00000354529.6:n.*146del
ENST00000673312.2:c.*1428del	ENSP00000500186.2:n.*1428del
ENST00000338641.10:c.*146del MANE Select	ENSP00000344666.5:n.*146del
ENST00000361166.9:c.1352del	ENSP00000354529.5:n.1352del
ENST00000672461.1:c.*206del	ENSP00000500919.1:n.*206del
ENST00000672896.1:c.*206del	ENSP00000500117.1:n.*206del
ENST00000673312.1:c.1953del	ENSP00000500186.1:n.1953del
ENST00000338641.8:c.*146del	ENSP00000344666.4:n.*146del
ENST00000361452.8:c.*206del	ENSP00000354897.4:n.*206del
ENST00000413209.6:c.*146del	ENSP00000409921.2:n.*146del
NM_000268.3:c.*146del , LRG_511t1:c.*146del	NP_000259.1:n.*146del
NM_016418.5:c.*206del , LRG_511t2:c.*206del	NP_057502.2:n.*206del
NM_181828.2:c.*206del	NP_861966.1:n.*206del
NM_181829.2:c.*206del	NP_861967.1:n.*206del
NM_181830.2:c.*206del	NP_861968.1:n.*206del
NM_181832.2:c.*221del	NP_861970.1:n.*221del
NM_181833.2:c.*146del	NP_861971.1:n.*146del
NR_156186.1:n.2493del
XM_017028809.2:c.*146del	XP_016884298.1:n.*146del
XM_017028810.1:c.*206del	XP_016884299.1:n.*206del
NM_000268.4:c.*146del MANE Select	NP_000259.1:n.*146del
NM_181828.3:c.*206del	NP_861966.1:n.*206del
NM_181829.3:c.*206del	NP_861967.1:n.*206del
NM_181830.3:c.*206del	NP_861968.1:n.*206del
NM_181832.3:c.*221del	NP_861970.1:n.*221del
NR_156186.2:n.2416del
NM_181833.3:c.*146del	NP_861971.1:n.*146del