Canonical Allele Identifier: CA1024928288

Gene: NF2

Linked Data

• dbSNP Id: rs11442202
• gnomAD v3: 22-29696824-GT-G
• gnomAD v4: 22-29696824-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29696834del , CM000684.2:g.29696834del	GRCh38
NC_000022.10:g.30092823del , CM000684.1:g.30092823del	GRCh37
NC_000022.9:g.28422823del	NCBI36
NG_009057.1:g.98279del , LRG_511:g.98279del

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*2032del MANE Select	ENSP00000344666.5:n.*2032del
ENST00000672461.1:c.*502-427del	ENSP00000500919.1:n.*502-427del
ENST00000672896.1:c.*2092del	ENSP00000500117.1:n.*2092del
ENST00000338641.8:c.*2032del	ENSP00000344666.4:n.*2032del
ENST00000361452.8:c.*2092del	ENSP00000354897.4:n.*2092del
ENST00000413209.6:c.*2032del	ENSP00000409921.2:n.*2032del
NM_000268.3:c.*2032del , LRG_511t1:c.*2032del	NP_000259.1:n.*2032del
NM_016418.5:c.*2092del , LRG_511t2:c.*2092del	NP_057502.2:n.*2092del
NM_181828.2:c.*2092del	NP_861966.1:n.*2092del
NM_181829.2:c.*2092del	NP_861967.1:n.*2092del
NM_181830.2:c.*2092del	NP_861968.1:n.*2092del
NM_181832.2:c.*2107del	NP_861970.1:n.*2107del
NM_181833.2:c.*2032del	NP_861971.1:n.*2032del
NR_156186.1:n.4379del
XM_017028810.1:c.*2092del	XP_016884299.1:n.*2092del
NM_000268.4:c.*2032del MANE Select	NP_000259.1:n.*2032del
NM_181828.3:c.*2092del	NP_861966.1:n.*2092del
NM_181829.3:c.*2092del	NP_861967.1:n.*2092del
NM_181830.3:c.*2092del	NP_861968.1:n.*2092del
NM_181832.3:c.*2107del	NP_861970.1:n.*2107del
NR_156186.2:n.4302del
NM_181833.3:c.*2032del	NP_861971.1:n.*2032del