Canonical Allele Identifier: CA2656032924

Gene: NF2

Linked Data

• gnomAD v4: 22-29694848-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694848G>A , CM000684.2:g.29694848G>A	GRCh38
NC_000022.10:g.30090837G>A , CM000684.1:g.30090837G>A	GRCh37
NC_000022.9:g.28420837G>A	NCBI36
NG_009057.1:g.96293G>A , LRG_511:g.96293G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*46G>A	ENSP00000354529.6:n.*46G>A
ENST00000673312.2:c.*1328G>A	ENSP00000500186.2:n.*1328G>A
ENST00000338641.10:c.*46G>A MANE Select	ENSP00000344666.5:n.*46G>A
ENST00000361166.9:c.1252G>A	ENSP00000354529.5:n.1252G>A
ENST00000672461.1:c.*106G>A	ENSP00000500919.1:n.*106G>A
ENST00000672805.1:c.*1716G>A	ENSP00000500295.1:n.*1716G>A
ENST00000672896.1:c.*106G>A	ENSP00000500117.1:n.*106G>A
ENST00000673312.1:c.1853G>A	ENSP00000500186.1:n.1853G>A
ENST00000338641.8:c.*46G>A	ENSP00000344666.4:n.*46G>A
ENST00000361452.8:c.*106G>A	ENSP00000354897.4:n.*106G>A
ENST00000413209.6:c.*46G>A	ENSP00000409921.2:n.*46G>A
ENST00000432151.5:c.*190G>A	ENSP00000395885.1:n.*190G>A
NM_000268.3:c.*46G>A , LRG_511t1:c.*46G>A	NP_000259.1:n.*46G>A
NM_016418.5:c.*106G>A , LRG_511t2:c.*106G>A	NP_057502.2:n.*106G>A
NM_181828.2:c.*106G>A	NP_861966.1:n.*106G>A
NM_181829.2:c.*106G>A	NP_861967.1:n.*106G>A
NM_181830.2:c.*106G>A	NP_861968.1:n.*106G>A
NM_181832.2:c.*121G>A	NP_861970.1:n.*121G>A
NM_181833.2:c.*46G>A	NP_861971.1:n.*46G>A
NR_156186.1:n.2393G>A
XM_017028809.2:c.*46G>A	XP_016884298.1:n.*46G>A
XM_017028810.1:c.*106G>A	XP_016884299.1:n.*106G>A
NM_000268.4:c.*46G>A MANE Select	NP_000259.1:n.*46G>A
NM_181828.3:c.*106G>A	NP_861966.1:n.*106G>A
NM_181829.3:c.*106G>A	NP_861967.1:n.*106G>A
NM_181830.3:c.*106G>A	NP_861968.1:n.*106G>A
NM_181832.3:c.*121G>A	NP_861970.1:n.*121G>A
NR_156186.2:n.2316G>A
NM_181833.3:c.*46G>A	NP_861971.1:n.*46G>A