Canonical Allele Identifier: CA2656033222

Gene: NF2

Linked Data

• gnomAD v4: 22-29695037-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29695037T>A , CM000684.2:g.29695037T>A	GRCh38
NC_000022.10:g.30091026T>A , CM000684.1:g.30091026T>A	GRCh37
NC_000022.9:g.28421026T>A	NCBI36
NG_009057.1:g.96482T>A , LRG_511:g.96482T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*235T>A	ENSP00000354529.6:n.*235T>A
ENST00000673312.2:c.*1517T>A	ENSP00000500186.2:n.*1517T>A
ENST00000338641.10:c.*235T>A MANE Select	ENSP00000344666.5:n.*235T>A
ENST00000361166.9:c.1441T>A	ENSP00000354529.5:n.1441T>A
ENST00000672461.1:c.*295T>A	ENSP00000500919.1:n.*295T>A
ENST00000672896.1:c.*295T>A	ENSP00000500117.1:n.*295T>A
ENST00000673312.1:c.2042T>A	ENSP00000500186.1:n.2042T>A
ENST00000338641.8:c.*235T>A	ENSP00000344666.4:n.*235T>A
ENST00000361452.8:c.*295T>A	ENSP00000354897.4:n.*295T>A
ENST00000413209.6:c.*235T>A	ENSP00000409921.2:n.*235T>A
NM_000268.3:c.*235T>A , LRG_511t1:c.*235T>A	NP_000259.1:n.*235T>A
NM_016418.5:c.*295T>A , LRG_511t2:c.*295T>A	NP_057502.2:n.*295T>A
NM_181828.2:c.*295T>A	NP_861966.1:n.*295T>A
NM_181829.2:c.*295T>A	NP_861967.1:n.*295T>A
NM_181830.2:c.*295T>A	NP_861968.1:n.*295T>A
NM_181832.2:c.*310T>A	NP_861970.1:n.*310T>A
NM_181833.2:c.*235T>A	NP_861971.1:n.*235T>A
NR_156186.1:n.2582T>A
XM_017028809.2:c.*235T>A	XP_016884298.1:n.*235T>A
XM_017028810.1:c.*295T>A	XP_016884299.1:n.*295T>A
NM_000268.4:c.*235T>A MANE Select	NP_000259.1:n.*235T>A
NM_181828.3:c.*295T>A	NP_861966.1:n.*295T>A
NM_181829.3:c.*295T>A	NP_861967.1:n.*295T>A
NM_181830.3:c.*295T>A	NP_861968.1:n.*295T>A
NM_181832.3:c.*310T>A	NP_861970.1:n.*310T>A
NR_156186.2:n.2505T>A
NM_181833.3:c.*235T>A	NP_861971.1:n.*235T>A