Canonical Allele Identifier: CA2255619342
Gene: NF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31334371_31334372delinsTC , CM000679.2:g.31334371_31334372delinsTC GRCh38
NC_000017.10:g.29661389_29661390delinsTC , CM000679.1:g.29661389_29661390delinsTC GRCh37
NC_000017.9:g.26685515_26685516delinsTC NCBI36
NG_009018.1:g.244395_244396delinsTC , LRG_214:g.244395_244396delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.2001-467_2001-466delinsTC ENSP00000492721.2:n.2001-467_2001-466delinsTC
ENST00000696138.1:c.5795-467_5795-466delinsTC ENSP00000512431.1:n.5795-467_5795-466delinsTC
ENST00000684826.1:c.377-467_377-466delinsTC ENSP00000509994.1:n.377-467_377-466delinsTC
ENST00000687027.1:c.-32-467_-32-466delinsTC ENSP00000508715.1:n.-32-467_-32-466delinsTC
ENST00000687863.1:n.2458-467_2458-466delinsTC
ENST00000691014.1:c.5843-467_5843-466delinsTC ENSP00000510595.1:n.5843-467_5843-466delinsTC
ENST00000693617.1:c.377-467_377-466delinsTC ENSP00000510031.1:n.377-467_377-466delinsTC
ENST00000358273.9:c.5813-467_5813-466delinsTC MANE Select ENSP00000351015.4:n.5813-467_5813-466delinsTC
ENST00000356175.7:c.5750-467_5750-466delinsTC ENSP00000348498.3:n.5750-467_5750-466delinsTC
ENST00000358273.8:c.5813-467_5813-466delinsTC ENSP00000351015.4:n.5813-467_5813-466delinsTC
ENST00000456735.6:c.4748-467_4748-466delinsTC ENSP00000389907.2:n.4748-467_4748-466delinsTC
ENST00000479536.2:c.171-293_171-292delinsTC
ENST00000579081.5:c.5949-467_5949-466delinsTC ENSP00000462408.1:n.5949-467_5949-466delinsTC
ENST00000581113.6:n.1130-467_1130-466delinsTC
NM_000267.3:c.5750-467_5750-466delinsTC , LRG_214t1:c.5750-467_5750-466delinsTC NP_000258.1:n.5750-467_5750-466delinsTC
NM_001042492.2:c.5813-467_5813-466delinsTC , LRG_214t2:c.5813-467_5813-466delinsTC NP_001035957.1:n.5813-467_5813-466delinsTC
XM_005257983.1:c.5813-467_5813-466delinsTC XP_005258040.1:n.5813-467_5813-466delinsTC
XM_005257984.1:c.5750-467_5750-466delinsTC XP_005258041.1:n.5750-467_5750-466delinsTC
XM_006721922.1:c.5843-467_5843-466delinsTC XP_006721985.1:n.5843-467_5843-466delinsTC
XM_006721923.2:c.5804-467_5804-466delinsTC XP_006721986.1:n.5804-467_5804-466delinsTC
XM_006721924.1:c.5843-467_5843-466delinsTC XP_006721987.1:n.5843-467_5843-466delinsTC
XM_006721925.1:c.5780-467_5780-466delinsTC XP_006721988.1:n.5780-467_5780-466delinsTC
XM_006721926.2:c.5843-467_5843-466delinsTC XP_006721989.1:n.5843-467_5843-466delinsTC
XM_006721927.1:c.5843-467_5843-466delinsTC XP_006721990.1:n.5843-467_5843-466delinsTC
XM_011524852.1:c.5840-467_5840-466delinsTC XP_011523154.1:n.5840-467_5840-466delinsTC
XM_011524853.1:c.5804-467_5804-466delinsTC XP_011523155.1:n.5804-467_5804-466delinsTC
XM_011524854.1:c.5804-467_5804-466delinsTC XP_011523156.1:n.5804-467_5804-466delinsTC
XM_011524855.1:c.5804-467_5804-466delinsTC XP_011523157.1:n.5804-467_5804-466delinsTC
XM_011524856.1:c.5804-467_5804-466delinsTC XP_011523158.1:n.5804-467_5804-466delinsTC
XM_011524857.1:c.5843-467_5843-466delinsTC XP_011523159.1:n.5843-467_5843-466delinsTC
NM_001042492.3:c.5813-467_5813-466delinsTC MANE Select NP_001035957.1:n.5813-467_5813-466delinsTC