Canonical Allele Identifier: CA2255619408
Gene: NF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31334546_31334548delinsATT , CM000679.2:g.31334546_31334548delinsATT GRCh38
NC_000017.10:g.29661564_29661566delinsATT , CM000679.1:g.29661564_29661566delinsATT GRCh37
NC_000017.9:g.26685690_26685692delinsATT NCBI36
NG_009018.1:g.244570_244572delinsATT , LRG_214:g.244570_244572delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.2001-292_2001-290delinsATT ENSP00000492721.2:n.2001-292_2001-290delinsATT
ENST00000696138.1:c.5795-292_5795-290delinsATT ENSP00000512431.1:n.5795-292_5795-290delinsATT
ENST00000684826.1:c.377-292_377-290delinsATT ENSP00000509994.1:n.377-292_377-290delinsATT
ENST00000687027.1:c.-32-292_-32-290delinsATT ENSP00000508715.1:n.-32-292_-32-290delinsATT
ENST00000687863.1:n.2458-292_2458-290delinsATT
ENST00000691014.1:c.5843-292_5843-290delinsATT ENSP00000510595.1:n.5843-292_5843-290delinsATT
ENST00000693617.1:c.377-292_377-290delinsATT ENSP00000510031.1:n.377-292_377-290delinsATT
ENST00000358273.9:c.5813-292_5813-290delinsATT MANE Select ENSP00000351015.4:n.5813-292_5813-290delinsATT
ENST00000356175.7:c.5750-292_5750-290delinsATT ENSP00000348498.3:n.5750-292_5750-290delinsATT
ENST00000358273.8:c.5813-292_5813-290delinsATT ENSP00000351015.4:n.5813-292_5813-290delinsATT
ENST00000456735.6:c.4748-292_4748-290delinsATT ENSP00000389907.2:n.4748-292_4748-290delinsATT
ENST00000479536.2:c.171-118_171-116delinsATT
ENST00000579081.5:c.5949-292_5949-290delinsATT ENSP00000462408.1:n.5949-292_5949-290delinsATT
ENST00000581113.6:n.1130-292_1130-290delinsATT
NM_000267.3:c.5750-292_5750-290delinsATT , LRG_214t1:c.5750-292_5750-290delinsATT NP_000258.1:n.5750-292_5750-290delinsATT
NM_001042492.2:c.5813-292_5813-290delinsATT , LRG_214t2:c.5813-292_5813-290delinsATT NP_001035957.1:n.5813-292_5813-290delinsATT
XM_005257983.1:c.5813-292_5813-290delinsATT XP_005258040.1:n.5813-292_5813-290delinsATT
XM_005257984.1:c.5750-292_5750-290delinsATT XP_005258041.1:n.5750-292_5750-290delinsATT
XM_006721922.1:c.5843-292_5843-290delinsATT XP_006721985.1:n.5843-292_5843-290delinsATT
XM_006721923.2:c.5804-292_5804-290delinsATT XP_006721986.1:n.5804-292_5804-290delinsATT
XM_006721924.1:c.5843-292_5843-290delinsATT XP_006721987.1:n.5843-292_5843-290delinsATT
XM_006721925.1:c.5780-292_5780-290delinsATT XP_006721988.1:n.5780-292_5780-290delinsATT
XM_006721926.2:c.5843-292_5843-290delinsATT XP_006721989.1:n.5843-292_5843-290delinsATT
XM_006721927.1:c.5843-292_5843-290delinsATT XP_006721990.1:n.5843-292_5843-290delinsATT
XM_011524852.1:c.5840-292_5840-290delinsATT XP_011523154.1:n.5840-292_5840-290delinsATT
XM_011524853.1:c.5804-292_5804-290delinsATT XP_011523155.1:n.5804-292_5804-290delinsATT
XM_011524854.1:c.5804-292_5804-290delinsATT XP_011523156.1:n.5804-292_5804-290delinsATT
XM_011524855.1:c.5804-292_5804-290delinsATT XP_011523157.1:n.5804-292_5804-290delinsATT
XM_011524856.1:c.5804-292_5804-290delinsATT XP_011523158.1:n.5804-292_5804-290delinsATT
XM_011524857.1:c.5843-292_5843-290delinsATT XP_011523159.1:n.5843-292_5843-290delinsATT
NM_001042492.3:c.5813-292_5813-290delinsATT MANE Select NP_001035957.1:n.5813-292_5813-290delinsATT