Canonical Allele Identifier: CA2400685434

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29678285T= , CM000684.2:g.29678285T=	GRCh38
NC_000022.10:g.30074274T= , CM000684.1:g.30074274T=	GRCh37
NC_000022.9:g.28404274T=	NCBI36
NG_009057.1:g.79730T= , LRG_511:g.79730T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.1401T=	ENSP00000354529.6:p.Thr467=
ENST00000673312.2:c.*1030T=	ENSP00000500186.2:n.*1030T=
ENST00000338641.10:c.1536T= MANE Select	ENSP00000344666.5:p.Thr512=
ENST00000361166.9:c.954T=	ENSP00000354529.5:p.Thr318=
ENST00000672461.1:c.1536T=	ENSP00000500919.1:p.Thr512=
ENST00000672805.1:c.*1418T=	ENSP00000500295.1:n.*1418T=
ENST00000672896.1:c.1536T=	ENSP00000500117.1:p.Thr512=
ENST00000673312.1:c.1555T=	ENSP00000500186.1:n.1555T=
ENST00000334961.11:c.1287T=	ENSP00000335652.7:p.Thr429=
ENST00000338641.8:c.1536T=	ENSP00000344666.4:p.Thr512=
ENST00000353887.8:c.1287T=	ENSP00000340626.4:p.Thr429=
ENST00000361166.8:c.1536T=	ENSP00000354529.4:p.Thr512=
ENST00000361452.8:c.1413T=	ENSP00000354897.4:p.Thr471=
ENST00000361676.8:c.1410T=	ENSP00000355183.4:p.Thr470=
ENST00000397789.3:c.1536T=	ENSP00000380891.3:p.Thr512=
ENST00000403435.5:c.1449T=	ENSP00000384029.1:p.Thr483=
ENST00000403999.7:c.1536T=	ENSP00000384797.3:p.Thr512=
ENST00000413209.6:c.448-16467T=	ENSP00000409921.2:n.448-16467T=
ENST00000432151.5:c.*55T=	ENSP00000395885.1:n.*55T=
NM_000268.3:c.1536T= , LRG_511t1:c.1536T=	NP_000259.1:p.Thr512=
NM_016418.5:c.1536T= , LRG_511t2:c.1536T=	NP_057502.2:p.Thr512=
NM_181825.2:c.1536T=	NP_861546.1:p.Thr512=
NM_181828.2:c.1410T=	NP_861966.1:p.Thr470=
NM_181829.2:c.1413T=	NP_861967.1:p.Thr471=
NM_181830.2:c.1287T=	NP_861968.1:p.Thr429=
NM_181831.2:c.1287T=	NP_861969.1:p.Thr429=
NM_181832.2:c.1536T=	NP_861970.1:p.Thr512=
NM_181833.2:c.448-16467T=	NP_861971.1:n.448-16467T=
NR_156186.1:n.2095T=
XM_017028809.2:c.1422T=	XP_016884298.1:p.Thr474=
XM_017028810.1:c.1422T=	XP_016884299.1:p.Thr474=
NM_000268.4:c.1536T= MANE Select	NP_000259.1:p.Thr512=
NM_181825.3:c.1536T=	NP_861546.1:p.Thr512=
NM_181828.3:c.1410T=	NP_861966.1:p.Thr470=
NM_181829.3:c.1413T=	NP_861967.1:p.Thr471=
NM_181830.3:c.1287T=	NP_861968.1:p.Thr429=
NM_181831.3:c.1287T=	NP_861969.1:p.Thr429=
NM_181832.3:c.1536T=	NP_861970.1:p.Thr512=
NR_156186.2:n.2018T=
NM_181833.3:c.448-16467T=	NP_861971.1:n.448-16467T=