Canonical Allele Identifier: CA2543062203

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694852C>G , CM000684.2:g.29694852C>G	GRCh38
NC_000022.10:g.30090841C>G , CM000684.1:g.30090841C>G	GRCh37
NC_000022.9:g.28420841C>G	NCBI36
NG_009057.1:g.96297C>G , LRG_511:g.96297C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*50C>G	ENSP00000354529.6:n.*50C>G
ENST00000673312.2:c.*1332C>G	ENSP00000500186.2:n.*1332C>G
ENST00000338641.10:c.*50C>G MANE Select	ENSP00000344666.5:n.*50C>G
ENST00000361166.9:c.1256C>G	ENSP00000354529.5:n.1256C>G
ENST00000672461.1:c.*110C>G	ENSP00000500919.1:n.*110C>G
ENST00000672805.1:c.*1720C>G	ENSP00000500295.1:n.*1720C>G
ENST00000672896.1:c.*110C>G	ENSP00000500117.1:n.*110C>G
ENST00000673312.1:c.1857C>G	ENSP00000500186.1:n.1857C>G
ENST00000338641.8:c.*50C>G	ENSP00000344666.4:n.*50C>G
ENST00000361452.8:c.*110C>G	ENSP00000354897.4:n.*110C>G
ENST00000413209.6:c.*50C>G	ENSP00000409921.2:n.*50C>G
ENST00000432151.5:c.*194C>G	ENSP00000395885.1:n.*194C>G
NM_000268.3:c.*50C>G , LRG_511t1:c.*50C>G	NP_000259.1:n.*50C>G
NM_016418.5:c.*110C>G , LRG_511t2:c.*110C>G	NP_057502.2:n.*110C>G
NM_181828.2:c.*110C>G	NP_861966.1:n.*110C>G
NM_181829.2:c.*110C>G	NP_861967.1:n.*110C>G
NM_181830.2:c.*110C>G	NP_861968.1:n.*110C>G
NM_181832.2:c.*125C>G	NP_861970.1:n.*125C>G
NM_181833.2:c.*50C>G	NP_861971.1:n.*50C>G
NR_156186.1:n.2397C>G
XM_017028809.2:c.*50C>G	XP_016884298.1:n.*50C>G
XM_017028810.1:c.*110C>G	XP_016884299.1:n.*110C>G
NM_000268.4:c.*50C>G MANE Select	NP_000259.1:n.*50C>G
NM_181828.3:c.*110C>G	NP_861966.1:n.*110C>G
NM_181829.3:c.*110C>G	NP_861967.1:n.*110C>G
NM_181830.3:c.*110C>G	NP_861968.1:n.*110C>G
NM_181832.3:c.*125C>G	NP_861970.1:n.*125C>G
NR_156186.2:n.2320C>G
NM_181833.3:c.*50C>G	NP_861971.1:n.*50C>G