Canonical Allele Identifier: CA2255619423

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31334585_31334586delinsGA , CM000679.2:g.31334585_31334586delinsGA	GRCh38
NC_000017.10:g.29661603_29661604delinsGA , CM000679.1:g.29661603_29661604delinsGA	GRCh37
NC_000017.9:g.26685729_26685730delinsGA	NCBI36
NG_009018.1:g.244609_244610delinsGA , LRG_214:g.244609_244610delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581113.7:c.2001-253_2001-252delinsGA	ENSP00000492721.2:n.2001-253_2001-252delinsGA
ENST00000696138.1:c.5795-253_5795-252delinsGA	ENSP00000512431.1:n.5795-253_5795-252delinsGA
ENST00000684826.1:c.377-253_377-252delinsGA	ENSP00000509994.1:n.377-253_377-252delinsGA
ENST00000687027.1:c.-32-253_-32-252delinsGA	ENSP00000508715.1:n.-32-253_-32-252delinsGA
ENST00000687863.1:n.2458-253_2458-252delinsGA
ENST00000691014.1:c.5843-253_5843-252delinsGA	ENSP00000510595.1:n.5843-253_5843-252delinsGA
ENST00000693617.1:c.377-253_377-252delinsGA	ENSP00000510031.1:n.377-253_377-252delinsGA
ENST00000358273.9:c.5813-253_5813-252delinsGA MANE Select	ENSP00000351015.4:n.5813-253_5813-252delinsGA
ENST00000356175.7:c.5750-253_5750-252delinsGA	ENSP00000348498.3:n.5750-253_5750-252delinsGA
ENST00000358273.8:c.5813-253_5813-252delinsGA	ENSP00000351015.4:n.5813-253_5813-252delinsGA
ENST00000456735.6:c.4748-253_4748-252delinsGA	ENSP00000389907.2:n.4748-253_4748-252delinsGA
ENST00000479536.2:c.171-79_171-78delinsGA
ENST00000579081.5:c.5949-253_5949-252delinsGA	ENSP00000462408.1:n.5949-253_5949-252delinsGA
ENST00000581113.6:n.1130-253_1130-252delinsGA
NM_000267.3:c.5750-253_5750-252delinsGA , LRG_214t1:c.5750-253_5750-252delinsGA	NP_000258.1:n.5750-253_5750-252delinsGA
NM_001042492.2:c.5813-253_5813-252delinsGA , LRG_214t2:c.5813-253_5813-252delinsGA	NP_001035957.1:n.5813-253_5813-252delinsGA
XM_005257983.1:c.5813-253_5813-252delinsGA	XP_005258040.1:n.5813-253_5813-252delinsGA
XM_005257984.1:c.5750-253_5750-252delinsGA	XP_005258041.1:n.5750-253_5750-252delinsGA
XM_006721922.1:c.5843-253_5843-252delinsGA	XP_006721985.1:n.5843-253_5843-252delinsGA
XM_006721923.2:c.5804-253_5804-252delinsGA	XP_006721986.1:n.5804-253_5804-252delinsGA
XM_006721924.1:c.5843-253_5843-252delinsGA	XP_006721987.1:n.5843-253_5843-252delinsGA
XM_006721925.1:c.5780-253_5780-252delinsGA	XP_006721988.1:n.5780-253_5780-252delinsGA
XM_006721926.2:c.5843-253_5843-252delinsGA	XP_006721989.1:n.5843-253_5843-252delinsGA
XM_006721927.1:c.5843-253_5843-252delinsGA	XP_006721990.1:n.5843-253_5843-252delinsGA
XM_011524852.1:c.5840-253_5840-252delinsGA	XP_011523154.1:n.5840-253_5840-252delinsGA
XM_011524853.1:c.5804-253_5804-252delinsGA	XP_011523155.1:n.5804-253_5804-252delinsGA
XM_011524854.1:c.5804-253_5804-252delinsGA	XP_011523156.1:n.5804-253_5804-252delinsGA
XM_011524855.1:c.5804-253_5804-252delinsGA	XP_011523157.1:n.5804-253_5804-252delinsGA
XM_011524856.1:c.5804-253_5804-252delinsGA	XP_011523158.1:n.5804-253_5804-252delinsGA
XM_011524857.1:c.5843-253_5843-252delinsGA	XP_011523159.1:n.5843-253_5843-252delinsGA
NM_001042492.3:c.5813-253_5813-252delinsGA MANE Select	NP_001035957.1:n.5813-253_5813-252delinsGA