Canonical Allele Identifier: CA645601095

Gene: NF2

Linked Data

• COSMIC: COSM24363

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29671829_29671915del , CM000684.2:g.29671829_29671915del	GRCh38
NC_000022.10:g.30067818_30067904del , CM000684.1:g.30067818_30067904del	GRCh37
NC_000022.9:g.28397818_28397904del	NCBI36
NG_009057.1:g.73274_73360del , LRG_511:g.73274_73360del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.868_954del
ENST00000673312.2:c.*497_*583del
ENST00000338641.10:c.1003_1089del
ENST00000361166.9:c.421_507del
ENST00000672461.1:c.1003_1089del
ENST00000672805.1:c.*885_*971del
ENST00000672896.1:c.1003_1089del
ENST00000673312.1:c.1022_1108del
ENST00000334961.11:c.754_840del
ENST00000338641.8:c.1003_1089del
ENST00000353887.8:c.754_840del
ENST00000361166.8:c.1003_1089del
ENST00000361452.8:c.880_966del
ENST00000361676.8:c.877_963del
ENST00000397789.3:c.1003_1089del
ENST00000403435.5:c.1000-84_1002del
ENST00000403999.7:c.1003_1089del
ENST00000413209.6:c.448-22923_448-22837del	ENSP00000409921.2:n.448-22923_448-22837de...
ENST00000432151.5:c.523-3007_523-2921del	ENSP00000395885.1:n.523-3007_523-2921del
NM_000268.3:c.1003_1089del , LRG_511t1:c.1003_1089del
NM_016418.5:c.1003_1089del , LRG_511t2:c.1003_1089del
NM_181825.2:c.1003_1089del
NM_181828.2:c.877_963del
NM_181829.2:c.880_966del
NM_181830.2:c.754_840del
NM_181831.2:c.754_840del
NM_181832.2:c.1003_1089del
NM_181833.2:c.448-22923_448-22837del	NP_861971.1:n.448-22923_448-22837del
NR_156186.1:n.1562_1648del
XM_017028809.2:c.889_975del
XM_017028810.1:c.889_975del
NM_000268.4:c.1003_1089del
NM_181825.3:c.1003_1089del
NM_181828.3:c.877_963del
NM_181829.3:c.880_966del
NM_181830.3:c.754_840del
NM_181831.3:c.754_840del
NM_181832.3:c.1003_1089del
NR_156186.2:n.1485_1571del
NM_181833.3:c.448-22923_448-22837del	NP_861971.1:n.448-22923_448-22837del