Canonical Allele Identifier: CA2809192332
Gene: NF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31201409_31201411del , CM000679.2:g.31201409_31201411del GRCh38
NC_000017.10:g.29528427_29528429del , CM000679.1:g.29528427_29528429del GRCh37
NC_000017.9:g.26552553_26552555del NCBI36
NG_009018.1:g.111433_111435del , LRG_214:g.111433_111435del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.1186-2_1186del
ENST00000686189.1:c.601-2_601del
ENST00000688507.1:n.892-2_892del
ENST00000691014.1:c.1186-2_1186del
ENST00000692326.1:n.1469-2_1469del
ENST00000358273.9:c.1186-2_1186del
ENST00000356175.7:c.1186-2_1186del
ENST00000358273.8:c.1186-2_1186del
ENST00000431387.8:c.1186-2_1186del
ENST00000456735.6:c.184-2_184del
ENST00000487476.5:n.1569-2_1569del
ENST00000495910.6:c.961-2_961del
ENST00000579081.5:c.1288-2_1288del
NM_000267.3:c.1186-2_1186del , LRG_214t1:c.1186-2_1186del
NM_001042492.2:c.1186-2_1186del , LRG_214t2:c.1186-2_1186del
NM_001128147.2:c.1186-2_1186del
XM_005257983.1:c.1186-2_1186del
XM_005257984.1:c.1186-2_1186del
XM_006721922.1:c.1186-2_1186del
XM_006721923.2:c.1147-2_1147del
XM_006721924.1:c.1186-2_1186del
XM_006721925.1:c.1186-2_1186del
XM_006721926.2:c.1186-2_1186del
XM_006721927.1:c.1186-2_1186del
XM_006721928.2:c.1186-2_1186del
XM_011524852.1:c.1186-2_1186del
XM_011524853.1:c.1147-2_1147del
XM_011524854.1:c.1147-2_1147del
XM_011524855.1:c.1147-2_1147del
XM_011524856.1:c.1147-2_1147del
XM_011524857.1:c.1186-2_1186del
NM_001042492.3:c.1186-2_1186del
NM_001128147.3:c.1186-2_1186del