Canonical Allele Identifier: CA2656032970

Gene: NF2

Linked Data

• gnomAD v4: 22-29694890-G-GTTTCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694890_29694891insTTTCCT , CM000684.2:g.29694890_29694891insTTTCCT	GRCh38
NC_000022.10:g.30090879_30090880insTTTCCT , CM000684.1:g.30090879_30090880insTTTCCT	GRCh37
NC_000022.9:g.28420879_28420880insTTTCCT	NCBI36
NG_009057.1:g.96335_96336insTTTCCT , LRG_511:g.96335_96336insTTTCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*88_*89insTTTCCT	ENSP00000354529.6:n.*88_*89insTTTCCT
ENST00000673312.2:c.*1370_*1371insTTTCCT	ENSP00000500186.2:n.*1370_*1371insTTTCCT
ENST00000338641.10:c.*88_*89insTTTCCT MANE Select	ENSP00000344666.5:n.*88_*89insTTTCCT
ENST00000361166.9:c.1294_1295insTTTCCT	ENSP00000354529.5:n.1294_1295insTTTCCT
ENST00000672461.1:c.*148_*149insTTTCCT	ENSP00000500919.1:n.*148_*149insTTTCCT
ENST00000672805.1:c.*1758_*1759insTTTCCT	ENSP00000500295.1:n.*1758_*1759insTTTCCT
ENST00000672896.1:c.*148_*149insTTTCCT	ENSP00000500117.1:n.*148_*149insTTTCCT
ENST00000673312.1:c.1895_1896insTTTCCT	ENSP00000500186.1:n.1895_1896insTTTCCT
ENST00000338641.8:c.*88_*89insTTTCCT	ENSP00000344666.4:n.*88_*89insTTTCCT
ENST00000361452.8:c.*148_*149insTTTCCT	ENSP00000354897.4:n.*148_*149insTTTCCT
ENST00000413209.6:c.*88_*89insTTTCCT	ENSP00000409921.2:n.*88_*89insTTTCCT
ENST00000432151.5:c.*232_*233insTTTCCT	ENSP00000395885.1:n.*232_*233insTTTCCT
NM_000268.3:c.*88_*89insTTTCCT , LRG_511t1:c.*88_*89insTTTCCT	NP_000259.1:n.*88_*89insTTTCCT
NM_016418.5:c.*148_*149insTTTCCT , LRG_511t2:c.*148_*149insTTTCCT	NP_057502.2:n.*148_*149insTTTCCT
NM_181828.2:c.*148_*149insTTTCCT	NP_861966.1:n.*148_*149insTTTCCT
NM_181829.2:c.*148_*149insTTTCCT	NP_861967.1:n.*148_*149insTTTCCT
NM_181830.2:c.*148_*149insTTTCCT	NP_861968.1:n.*148_*149insTTTCCT
NM_181832.2:c.*163_*164insTTTCCT	NP_861970.1:n.*163_*164insTTTCCT
NM_181833.2:c.*88_*89insTTTCCT	NP_861971.1:n.*88_*89insTTTCCT
NR_156186.1:n.2435_2436insTTTCCT
XM_017028809.2:c.*88_*89insTTTCCT	XP_016884298.1:n.*88_*89insTTTCCT
XM_017028810.1:c.*148_*149insTTTCCT	XP_016884299.1:n.*148_*149insTTTCCT
NM_000268.4:c.*88_*89insTTTCCT MANE Select	NP_000259.1:n.*88_*89insTTTCCT
NM_181828.3:c.*148_*149insTTTCCT	NP_861966.1:n.*148_*149insTTTCCT
NM_181829.3:c.*148_*149insTTTCCT	NP_861967.1:n.*148_*149insTTTCCT
NM_181830.3:c.*148_*149insTTTCCT	NP_861968.1:n.*148_*149insTTTCCT
NM_181832.3:c.*163_*164insTTTCCT	NP_861970.1:n.*163_*164insTTTCCT
NR_156186.2:n.2358_2359insTTTCCT
NM_181833.3:c.*88_*89insTTTCCT	NP_861971.1:n.*88_*89insTTTCCT