Canonical Allele Identifier: CA2255538655
Gene: NF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31155937T= , CM000679.2:g.31155937T= GRCh38
NC_000017.10:g.29482955T= , CM000679.1:g.29482955T= GRCh37
NC_000017.9:g.26507081T= NCBI36
NG_009018.1:g.65961T= , LRG_214:g.65961T=

Transcript Alleles

HGVS Amino-acid change
ENST00000696138.1:c.61-46T= ENSP00000512431.1:n.61-46T=
ENST00000691014.1:c.61-46T= ENSP00000510595.1:n.61-46T=
ENST00000358273.9:c.61-46T= MANE Select ENSP00000351015.4:n.61-46T=
ENST00000356175.7:c.61-46T= ENSP00000348498.3:n.61-46T=
ENST00000358273.8:c.61-46T= ENSP00000351015.4:n.61-46T=
ENST00000431387.8:c.61-46T= ENSP00000412921.4:n.61-46T=
ENST00000487476.5:n.444-46T=
ENST00000489712.6:c.-141-46T= ENSP00000467284.1:n.-141-46T=
ENST00000579081.5:c.163-46T= ENSP00000462408.1:n.163-46T=
NM_000267.3:c.61-46T= , LRG_214t1:c.61-46T= NP_000258.1:n.61-46T=
NM_001042492.2:c.61-46T= , LRG_214t2:c.61-46T= NP_001035957.1:n.61-46T=
NM_001128147.2:c.61-46T= NP_001121619.1:n.61-46T=
XM_005257983.1:c.61-46T= XP_005258040.1:n.61-46T=
XM_005257984.1:c.61-46T= XP_005258041.1:n.61-46T=
XM_006721922.1:c.61-46T= XP_006721985.1:n.61-46T=
XM_006721923.2:c.22-46T= XP_006721986.1:n.22-46T=
XM_006721924.1:c.61-46T= XP_006721987.1:n.61-46T=
XM_006721925.1:c.61-46T= XP_006721988.1:n.61-46T=
XM_006721926.2:c.61-46T= XP_006721989.1:n.61-46T=
XM_006721927.1:c.61-46T= XP_006721990.1:n.61-46T=
XM_006721928.2:c.61-46T= XP_006721991.1:n.61-46T=
XM_011524852.1:c.61-46T= XP_011523154.1:n.61-46T=
XM_011524853.1:c.22-46T= XP_011523155.1:n.22-46T=
XM_011524854.1:c.22-46T= XP_011523156.1:n.22-46T=
XM_011524855.1:c.22-46T= XP_011523157.1:n.22-46T=
XM_011524856.1:c.22-46T= XP_011523158.1:n.22-46T=
XM_011524857.1:c.61-46T= XP_011523159.1:n.61-46T=
NM_001042492.3:c.61-46T= MANE Select NP_001035957.1:n.61-46T=
NM_001128147.3:c.61-46T= NP_001121619.1:n.61-46T=