Canonical Allele Identifier: CA2400692892

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29696044_29696045delinsTG , CM000684.2:g.29696044_29696045delinsTG	GRCh38
NC_000022.10:g.30092033_30092034delinsTG , CM000684.1:g.30092033_30092034delinsTG	GRCh37
NC_000022.9:g.28422033_28422034delinsTG	NCBI36
NG_009057.1:g.97489_97490delinsTG , LRG_511:g.97489_97490delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000338641.10:c.*1242_*1243delinsTG MANE Select	ENSP00000344666.5:n.*1242_*1243delinsTG
ENST00000672461.1:c.*501+801_*501+802delinsTG	ENSP00000500919.1:n.*501+801_*501+802deli...
ENST00000672896.1:c.*1302_*1303delinsTG	ENSP00000500117.1:n.*1302_*1303delinsTG
ENST00000338641.8:c.*1242_*1243delinsTG	ENSP00000344666.4:n.*1242_*1243delinsTG
ENST00000361452.8:c.*1302_*1303delinsTG	ENSP00000354897.4:n.*1302_*1303delinsTG
ENST00000413209.6:c.*1242_*1243delinsTG	ENSP00000409921.2:n.*1242_*1243delinsTG
NM_000268.3:c.*1242_*1243delinsTG , LRG_511t1:c.*1242_*1243delinsTG	NP_000259.1:n.*1242_*1243delinsTG
NM_016418.5:c.*1302_*1303delinsTG , LRG_511t2:c.*1302_*1303delinsTG	NP_057502.2:n.*1302_*1303delinsTG
NM_181828.2:c.*1302_*1303delinsTG	NP_861966.1:n.*1302_*1303delinsTG
NM_181829.2:c.*1302_*1303delinsTG	NP_861967.1:n.*1302_*1303delinsTG
NM_181830.2:c.*1302_*1303delinsTG	NP_861968.1:n.*1302_*1303delinsTG
NM_181832.2:c.*1317_*1318delinsTG	NP_861970.1:n.*1317_*1318delinsTG
NM_181833.2:c.*1242_*1243delinsTG	NP_861971.1:n.*1242_*1243delinsTG
NR_156186.1:n.3589_3590delinsTG
XM_017028810.1:c.*1302_*1303delinsTG	XP_016884299.1:n.*1302_*1303delinsTG
NM_000268.4:c.*1242_*1243delinsTG MANE Select	NP_000259.1:n.*1242_*1243delinsTG
NM_181828.3:c.*1302_*1303delinsTG	NP_861966.1:n.*1302_*1303delinsTG
NM_181829.3:c.*1302_*1303delinsTG	NP_861967.1:n.*1302_*1303delinsTG
NM_181830.3:c.*1302_*1303delinsTG	NP_861968.1:n.*1302_*1303delinsTG
NM_181832.3:c.*1317_*1318delinsTG	NP_861970.1:n.*1317_*1318delinsTG
NR_156186.2:n.3512_3513delinsTG
NM_181833.3:c.*1242_*1243delinsTG	NP_861971.1:n.*1242_*1243delinsTG