Canonical Allele Identifier: CA645601094

Gene: NF2

Linked Data

• COSMIC: COSM23983

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29668439_29668447del , CM000684.2:g.29668439_29668447del	GRCh38
NC_000022.10:g.30064428_30064436del , CM000684.1:g.30064428_30064436del	GRCh37
NC_000022.9:g.28394428_28394436del	NCBI36
NG_009057.1:g.69884_69892del , LRG_511:g.69884_69892del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.857_864+1del
ENST00000673312.2:c.*486_*493+1del
ENST00000338641.10:c.992_999+1del
ENST00000361166.9:c.410_417+1del
ENST00000672461.1:c.992_999+1del
ENST00000672805.1:c.*874_*881+1del
ENST00000672896.1:c.992_999+1del
ENST00000673312.1:c.1011_1018+1del
ENST00000334961.11:c.743_750+1del
ENST00000338641.8:c.992_999+1del
ENST00000353887.8:c.743_750+1del
ENST00000361166.8:c.992_999+1del
ENST00000361452.8:c.869_876+1del
ENST00000361676.8:c.866_873+1del
ENST00000397789.3:c.992_999+1del
ENST00000403435.5:c.992_999+1del
ENST00000403999.7:c.992_999+1del
ENST00000413209.6:c.447+26154_447+26162del	ENSP00000409921.2:n.447+26154_447+26162del
ENST00000432151.5:c.515_522+1del
NM_000268.3:c.992_999+1del , LRG_511t1:c.992_999+1del
NM_016418.5:c.992_999+1del , LRG_511t2:c.992_999+1del
NM_181825.2:c.992_999+1del
NM_181828.2:c.866_873+1del
NM_181829.2:c.869_876+1del
NM_181830.2:c.743_750+1del
NM_181831.2:c.743_750+1del
NM_181832.2:c.992_999+1del
NM_181833.2:c.447+26154_447+26162del	NP_861971.1:n.447+26154_447+26162del
NR_156186.1:n.1551_1558+1del
XM_017028809.2:c.878_885+1del
XM_017028810.1:c.878_885+1del
NM_000268.4:c.992_999+1del
NM_181825.3:c.992_999+1del
NM_181828.3:c.866_873+1del
NM_181829.3:c.869_876+1del
NM_181830.3:c.743_750+1del
NM_181831.3:c.743_750+1del
NM_181832.3:c.992_999+1del
NR_156186.2:n.1474_1481+1del
NM_181833.3:c.447+26154_447+26162del	NP_861971.1:n.447+26154_447+26162del