Canonical Allele Identifier: CA2400678198

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29661346_29661348delinsCAT , CM000684.2:g.29661346_29661348delinsCAT	GRCh38
NC_000022.10:g.30057335_30057337delinsCAT , CM000684.1:g.30057335_30057337delinsCAT	GRCh37
NC_000022.9:g.28387335_28387337delinsCAT	NCBI36
NG_009057.1:g.62791_62793delinsCAT , LRG_511:g.62791_62793delinsCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.675+3082_675+3084delinsCAT	ENSP00000354529.6:n.675+3082_675+3084deli...
ENST00000673312.2:c.*304+7_*304+9delinsCAT	ENSP00000500186.2:n.*304+7_*304+9delinsCA...
ENST00000338641.10:c.810+7_810+9delinsCAT MANE Select	ENSP00000344666.5:n.810+7_810+9delinsCAT
ENST00000361166.9:c.228+3082_228+3084delinsCAT	ENSP00000354529.5:n.228+3082_228+3084deli...
ENST00000672461.1:c.810+7_810+9delinsCAT	ENSP00000500919.1:n.810+7_810+9delinsCAT
ENST00000672805.1:c.*692+7_*692+9delinsCAT	ENSP00000500295.1:n.*692+7_*692+9delinsCA...
ENST00000672896.1:c.810+7_810+9delinsCAT	ENSP00000500117.1:n.810+7_810+9delinsCAT
ENST00000673312.1:c.829+7_829+9delinsCAT	ENSP00000500186.1:n.829+7_829+9delinsCAT
ENST00000334961.11:c.561+7_561+9delinsCAT	ENSP00000335652.7:n.561+7_561+9delinsCAT
ENST00000338641.8:c.810+7_810+9delinsCAT	ENSP00000344666.4:n.810+7_810+9delinsCAT
ENST00000353887.8:c.561+7_561+9delinsCAT	ENSP00000340626.4:n.561+7_561+9delinsCAT
ENST00000361166.8:c.810+7_810+9delinsCAT	ENSP00000354529.4:n.810+7_810+9delinsCAT
ENST00000361452.8:c.687+7_687+9delinsCAT	ENSP00000354897.4:n.687+7_687+9delinsCAT
ENST00000361676.8:c.684+7_684+9delinsCAT	ENSP00000355183.4:n.684+7_684+9delinsCAT
ENST00000397789.3:c.810+7_810+9delinsCAT	ENSP00000380891.3:n.810+7_810+9delinsCAT
ENST00000403435.5:c.810+7_810+9delinsCAT	ENSP00000384029.1:n.810+7_810+9delinsCAT
ENST00000403999.7:c.810+7_810+9delinsCAT	ENSP00000384797.3:n.810+7_810+9delinsCAT
ENST00000413209.6:c.447+19061_447+19063delinsCAT	ENSP00000409921.2:n.447+19061_447+19063de...
ENST00000432151.5:c.333+7_333+9delinsCAT	ENSP00000395885.1:n.333+7_333+9delinsCAT
NM_000268.3:c.810+7_810+9delinsCAT , LRG_511t1:c.810+7_810+9delinsCAT	NP_000259.1:n.810+7_810+9delinsCAT
NM_016418.5:c.810+7_810+9delinsCAT , LRG_511t2:c.810+7_810+9delinsCAT	NP_057502.2:n.810+7_810+9delinsCAT
NM_181825.2:c.810+7_810+9delinsCAT	NP_861546.1:n.810+7_810+9delinsCAT
NM_181828.2:c.684+7_684+9delinsCAT	NP_861966.1:n.684+7_684+9delinsCAT
NM_181829.2:c.687+7_687+9delinsCAT	NP_861967.1:n.687+7_687+9delinsCAT
NM_181830.2:c.561+7_561+9delinsCAT	NP_861968.1:n.561+7_561+9delinsCAT
NM_181831.2:c.561+7_561+9delinsCAT	NP_861969.1:n.561+7_561+9delinsCAT
NM_181832.2:c.810+7_810+9delinsCAT	NP_861970.1:n.810+7_810+9delinsCAT
NM_181833.2:c.447+19061_447+19063delinsCAT	NP_861971.1:n.447+19061_447+19063delinsCA...
NR_156186.1:n.1369+7_1369+9delinsCAT
XM_017028809.2:c.696+7_696+9delinsCAT	XP_016884298.1:n.696+7_696+9delinsCAT
XM_017028810.1:c.696+7_696+9delinsCAT	XP_016884299.1:n.696+7_696+9delinsCAT
NM_000268.4:c.810+7_810+9delinsCAT MANE Select	NP_000259.1:n.810+7_810+9delinsCAT
NM_181825.3:c.810+7_810+9delinsCAT	NP_861546.1:n.810+7_810+9delinsCAT
NM_181828.3:c.684+7_684+9delinsCAT	NP_861966.1:n.684+7_684+9delinsCAT
NM_181829.3:c.687+7_687+9delinsCAT	NP_861967.1:n.687+7_687+9delinsCAT
NM_181830.3:c.561+7_561+9delinsCAT	NP_861968.1:n.561+7_561+9delinsCAT
NM_181831.3:c.561+7_561+9delinsCAT	NP_861969.1:n.561+7_561+9delinsCAT
NM_181832.3:c.810+7_810+9delinsCAT	NP_861970.1:n.810+7_810+9delinsCAT
NR_156186.2:n.1292+7_1292+9delinsCAT
NM_181833.3:c.447+19061_447+19063delinsCAT	NP_861971.1:n.447+19061_447+19063delinsCA...