Canonical Allele Identifier: CA399001386
Gene: NF1 HGNC NCBI

Linked Data

dbSNP Id: rs876659197

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31265336G>C , CM000679.2:g.31265336G>C GRCh38
NC_000017.10:g.29592354G>C , CM000679.1:g.29592354G>C GRCh37
NC_000017.9:g.26616480G>C NCBI36
NG_009018.1:g.175360G>C , LRG_214:g.175360G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.634G>C ENSP00000492721.2:n.634G>C
ENST00000696138.1:c.4814G>C ENSP00000512431.1:p.Arg1605Pro
ENST00000696140.1:n.938G>C
ENST00000696141.1:c.823G>C
ENST00000687863.1:n.1477G>C
ENST00000691014.1:c.4862G>C ENSP00000510595.1:p.Arg1621Pro
ENST00000358273.9:c.4832G>C MANE Select ENSP00000351015.4:p.Arg1611Pro
ENST00000356175.7:c.4769G>C ENSP00000348498.3:p.Arg1590Pro
ENST00000358273.8:c.4832G>C ENSP00000351015.4:p.Arg1611Pro
ENST00000456735.6:c.3767G>C ENSP00000389907.2:p.Arg1256Pro
ENST00000493220.5:n.3305G>C
ENST00000579081.5:c.4871G>C ENSP00000462408.1:p.Arg1624Pro
NM_000267.3:c.4769G>C , LRG_214t1:c.4769G>C NP_000258.1:p.Arg1590Pro
NM_001042492.2:c.4832G>C , LRG_214t2:c.4832G>C NP_001035957.1:p.Arg1611Pro
XM_005257983.1:c.4832G>C XP_005258040.1:p.Arg1611Pro
XM_005257984.1:c.4769G>C XP_005258041.1:p.Arg1590Pro
XM_006721922.1:c.4862G>C XP_006721985.1:p.Arg1621Pro
XM_006721923.2:c.4823G>C XP_006721986.1:p.Arg1608Pro
XM_006721924.1:c.4862G>C XP_006721987.1:p.Arg1621Pro
XM_006721925.1:c.4799G>C XP_006721988.1:p.Arg1600Pro
XM_006721926.2:c.4862G>C XP_006721989.1:p.Arg1621Pro
XM_006721927.1:c.4862G>C XP_006721990.1:p.Arg1621Pro
XM_006721928.2:c.4862G>C XP_006721991.1:p.Arg1621Pro
XM_011524852.1:c.4859G>C XP_011523154.1:p.Arg1620Pro
XM_011524853.1:c.4823G>C XP_011523155.1:p.Arg1608Pro
XM_011524854.1:c.4823G>C XP_011523156.1:p.Arg1608Pro
XM_011524855.1:c.4823G>C XP_011523157.1:p.Arg1608Pro
XM_011524856.1:c.4823G>C XP_011523158.1:p.Arg1608Pro
XM_011524857.1:c.4862G>C XP_011523159.1:p.Arg1621Pro
NM_001042492.3:c.4832G>C MANE Select NP_001035957.1:p.Arg1611Pro