Canonical Allele Identifier: CA2695224914
Gene: NF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31233148_31233150del , CM000679.2:g.31233148_31233150del GRCh38
NC_000017.10:g.29560166_29560168del , CM000679.1:g.29560166_29560168del GRCh37
NC_000017.9:g.26584292_26584294del NCBI36
NG_009018.1:g.143172_143174del , LRG_214:g.143172_143174del

Transcript Alleles

HGVS Amino-acid change
ENST00000696138.1:c.3688_3690del ENSP00000512431.1:p.Met1230del
ENST00000696139.1:c.988_990del ENSP00000512432.1:p.Met330del
ENST00000691014.1:c.3673_3675del ENSP00000510595.1:p.Met1225del
ENST00000693210.1:n.369_371del
ENST00000358273.9:c.3643_3645del MANE Select ENSP00000351015.4:p.Met1215del
ENST00000356175.7:c.3643_3645del ENSP00000348498.3:p.Met1215del
ENST00000358273.8:c.3643_3645del ENSP00000351015.4:p.Met1215del
ENST00000456735.6:c.2641_2643del ENSP00000389907.2:p.Met881del
ENST00000466819.5:c.119_121del
ENST00000479614.1:c.119_121del
ENST00000493220.5:n.2179_2181del
ENST00000495910.6:c.3418_3420del
ENST00000579081.5:c.3745_3747del ENSP00000462408.1:p.Met1249del
NM_000267.3:c.3643_3645del , LRG_214t1:c.3643_3645del NP_000258.1:p.Met1215del
NM_001042492.2:c.3643_3645del , LRG_214t2:c.3643_3645del NP_001035957.1:p.Met1215del
XM_005257983.1:c.3643_3645del XP_005258040.1:p.Met1215del
XM_005257984.1:c.3643_3645del XP_005258041.1:p.Met1215del
XM_006721922.1:c.3673_3675del XP_006721985.1:p.Met1225del
XM_006721923.2:c.3634_3636del XP_006721986.1:p.Met1212del
XM_006721924.1:c.3673_3675del XP_006721987.1:p.Met1225del
XM_006721925.1:c.3673_3675del XP_006721988.1:p.Met1225del
XM_006721926.2:c.3673_3675del XP_006721989.1:p.Met1225del
XM_006721927.1:c.3673_3675del XP_006721990.1:p.Met1225del
XM_006721928.2:c.3673_3675del XP_006721991.1:p.Met1225del
XM_011524852.1:c.3670_3672del XP_011523154.1:p.Met1224del
XM_011524853.1:c.3634_3636del XP_011523155.1:p.Met1212del
XM_011524854.1:c.3634_3636del XP_011523156.1:p.Met1212del
XM_011524855.1:c.3634_3636del XP_011523157.1:p.Met1212del
XM_011524856.1:c.3634_3636del XP_011523158.1:p.Met1212del
XM_011524857.1:c.3673_3675del XP_011523159.1:p.Met1225del
NM_001042492.3:c.3643_3645del MANE Select NP_001035957.1:p.Met1215del