Canonical Allele Identifier: CA2656033095

Gene: NF2

Linked Data

• gnomAD v4: 22-29694955-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694955T>C , CM000684.2:g.29694955T>C	GRCh38
NC_000022.10:g.30090944T>C , CM000684.1:g.30090944T>C	GRCh37
NC_000022.9:g.28420944T>C	NCBI36
NG_009057.1:g.96400T>C , LRG_511:g.96400T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*153T>C	ENSP00000354529.6:n.*153T>C
ENST00000673312.2:c.*1435T>C	ENSP00000500186.2:n.*1435T>C
ENST00000338641.10:c.*153T>C MANE Select	ENSP00000344666.5:n.*153T>C
ENST00000361166.9:c.1359T>C	ENSP00000354529.5:n.1359T>C
ENST00000672461.1:c.*213T>C	ENSP00000500919.1:n.*213T>C
ENST00000672896.1:c.*213T>C	ENSP00000500117.1:n.*213T>C
ENST00000673312.1:c.1960T>C	ENSP00000500186.1:n.1960T>C
ENST00000338641.8:c.*153T>C	ENSP00000344666.4:n.*153T>C
ENST00000361452.8:c.*213T>C	ENSP00000354897.4:n.*213T>C
ENST00000413209.6:c.*153T>C	ENSP00000409921.2:n.*153T>C
NM_000268.3:c.*153T>C , LRG_511t1:c.*153T>C	NP_000259.1:n.*153T>C
NM_016418.5:c.*213T>C , LRG_511t2:c.*213T>C	NP_057502.2:n.*213T>C
NM_181828.2:c.*213T>C	NP_861966.1:n.*213T>C
NM_181829.2:c.*213T>C	NP_861967.1:n.*213T>C
NM_181830.2:c.*213T>C	NP_861968.1:n.*213T>C
NM_181832.2:c.*228T>C	NP_861970.1:n.*228T>C
NM_181833.2:c.*153T>C	NP_861971.1:n.*153T>C
NR_156186.1:n.2500T>C
XM_017028809.2:c.*153T>C	XP_016884298.1:n.*153T>C
XM_017028810.1:c.*213T>C	XP_016884299.1:n.*213T>C
NM_000268.4:c.*153T>C MANE Select	NP_000259.1:n.*153T>C
NM_181828.3:c.*213T>C	NP_861966.1:n.*213T>C
NM_181829.3:c.*213T>C	NP_861967.1:n.*213T>C
NM_181830.3:c.*213T>C	NP_861968.1:n.*213T>C
NM_181832.3:c.*228T>C	NP_861970.1:n.*228T>C
NR_156186.2:n.2423T>C
NM_181833.3:c.*153T>C	NP_861971.1:n.*153T>C