Canonical Allele Identifier: CA645601056

Gene: NF2

Linked Data

• COSMIC: COSM23981

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29661195_29661255del , CM000684.2:g.29661195_29661255del	GRCh38
NC_000022.10:g.30057184_30057244del , CM000684.1:g.30057184_30057244del	GRCh37
NC_000022.9:g.28387184_28387244del	NCBI36
NG_009057.1:g.62640_62700del , LRG_511:g.62640_62700del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.675+2931_675+2991del	ENSP00000354529.6:n.675+2931_675+2991del
ENST00000673312.2:c.*170-10_*220del
ENST00000338641.10:c.676-10_726del
ENST00000361166.9:c.228+2931_228+2991del	ENSP00000354529.5:n.228+2931_228+2991del
ENST00000672461.1:c.676-10_726del
ENST00000672805.1:c.*558-10_*608del
ENST00000672896.1:c.676-10_726del
ENST00000673312.1:c.695-10_745del
ENST00000334961.11:c.427-10_477del
ENST00000338641.8:c.676-10_726del
ENST00000353887.8:c.427-10_477del
ENST00000361166.8:c.676-10_726del
ENST00000361452.8:c.553-10_603del
ENST00000361676.8:c.550-10_600del
ENST00000397789.3:c.676-10_726del
ENST00000403435.5:c.676-10_726del
ENST00000403999.7:c.676-10_726del
ENST00000413209.6:c.447+18910_447+18970del	ENSP00000409921.2:n.447+18910_447+18970de...
ENST00000432151.5:c.199-10_249del
NM_000268.3:c.676-10_726del , LRG_511t1:c.676-10_726del
NM_016418.5:c.676-10_726del , LRG_511t2:c.676-10_726del
NM_181825.2:c.676-10_726del
NM_181828.2:c.550-10_600del
NM_181829.2:c.553-10_603del
NM_181830.2:c.427-10_477del
NM_181831.2:c.427-10_477del
NM_181832.2:c.676-10_726del
NM_181833.2:c.447+18910_447+18970del	NP_861971.1:n.447+18910_447+18970del
NR_156186.1:n.1235-10_1285del
XM_017028809.2:c.562-10_612del
XM_017028810.1:c.562-10_612del
NM_000268.4:c.676-10_726del
NM_181825.3:c.676-10_726del
NM_181828.3:c.550-10_600del
NM_181829.3:c.553-10_603del
NM_181830.3:c.427-10_477del
NM_181831.3:c.427-10_477del
NM_181832.3:c.676-10_726del
NR_156186.2:n.1158-10_1208del
NM_181833.3:c.447+18910_447+18970del	NP_861971.1:n.447+18910_447+18970del