Canonical Allele Identifier: CA2695225377
Gene: NF1 HGNC NCBI

Linked Data

dbSNP Id: rs2151429172

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31229196del , CM000679.2:g.31229196del GRCh38
NC_000017.10:g.29556214del , CM000679.1:g.29556214del GRCh37
NC_000017.9:g.26580340del NCBI36
NG_009018.1:g.139220del , LRG_214:g.139220del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.2626del ENSP00000512431.1:p.Ala876GlnfsTer17
ENST00000691014.1:c.2611del ENSP00000510595.1:p.Ala871GlnfsTer17
ENST00000358273.9:c.2581del MANE Select ENSP00000351015.4:p.Ala861GlnfsTer17
ENST00000356175.7:c.2581del ENSP00000348498.3:p.Ala861GlnfsTer17
ENST00000358273.8:c.2581del ENSP00000351015.4:p.Ala861GlnfsTer17
ENST00000456735.6:c.1579del ENSP00000389907.2:p.Ala527GlnfsTer17
ENST00000493220.5:n.748del
ENST00000495910.6:c.2356del
ENST00000579081.5:c.2683del ENSP00000462408.1:p.Ala895GlnfsTer17
NM_000267.3:c.2581del , LRG_214t1:c.2581del NP_000258.1:p.Ala861GlnfsTer17
NM_001042492.2:c.2581del , LRG_214t2:c.2581del NP_001035957.1:p.Ala861GlnfsTer17
XM_005257983.1:c.2581del XP_005258040.1:p.Ala861GlnfsTer17
XM_005257984.1:c.2581del XP_005258041.1:p.Ala861GlnfsTer17
XM_006721922.1:c.2611del XP_006721985.1:p.Ala871GlnfsTer17
XM_006721923.2:c.2572del XP_006721986.1:p.Ala858GlnfsTer17
XM_006721924.1:c.2611del XP_006721987.1:p.Ala871GlnfsTer17
XM_006721925.1:c.2611del XP_006721988.1:p.Ala871GlnfsTer17
XM_006721926.2:c.2611del XP_006721989.1:p.Ala871GlnfsTer17
XM_006721927.1:c.2611del XP_006721990.1:p.Ala871GlnfsTer17
XM_006721928.2:c.2611del XP_006721991.1:p.Ala871GlnfsTer17
XM_011524852.1:c.2608del XP_011523154.1:p.Ala870GlnfsTer17
XM_011524853.1:c.2572del XP_011523155.1:p.Ala858GlnfsTer17
XM_011524854.1:c.2572del XP_011523156.1:p.Ala858GlnfsTer17
XM_011524855.1:c.2572del XP_011523157.1:p.Ala858GlnfsTer17
XM_011524856.1:c.2572del XP_011523158.1:p.Ala858GlnfsTer17
XM_011524857.1:c.2611del XP_011523159.1:p.Ala871GlnfsTer17
NM_001042492.3:c.2581del MANE Select NP_001035957.1:p.Ala861GlnfsTer17