Canonical Allele Identifier: CA2841510090

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31265340_31265350del , CM000679.2:g.31265340_31265350del	GRCh38
NC_000017.10:g.29592358_29592368del , CM000679.1:g.29592358_29592368del	GRCh37
NC_000017.9:g.26616484_26616494del	NCBI36
NG_009018.1:g.175364_175374del , LRG_214:g.175364_175374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581113.7:c.637+1_637+11del	ENSP00000492721.2:n.637+1_637+11del
ENST00000696138.1:c.4817+1_4817+11del	ENSP00000512431.1:n.4817+1_4817+11del
ENST00000696140.1:n.941+1_941+11del
ENST00000696141.1:c.826+1_826+11del
ENST00000687863.1:n.1480+1_1480+11del
ENST00000691014.1:c.4865+1_4865+11del	ENSP00000510595.1:n.4865+1_4865+11del
ENST00000358273.9:c.4835+1_4835+11del MANE Select	ENSP00000351015.4:n.4835+1_4835+11del
ENST00000356175.7:c.4772+1_4772+11del	ENSP00000348498.3:n.4772+1_4772+11del
ENST00000358273.8:c.4835+1_4835+11del	ENSP00000351015.4:n.4835+1_4835+11del
ENST00000456735.6:c.3770+1_3770+11del	ENSP00000389907.2:n.3770+1_3770+11del
ENST00000493220.5:n.3308+1_3308+11del
ENST00000579081.5:c.4874+1_4874+11del	ENSP00000462408.1:n.4874+1_4874+11del
NM_000267.3:c.4772+1_4772+11del , LRG_214t1:c.4772+1_4772+11del	NP_000258.1:n.4772+1_4772+11del
NM_001042492.2:c.4835+1_4835+11del , LRG_214t2:c.4835+1_4835+11del	NP_001035957.1:n.4835+1_4835+11del
XM_005257983.1:c.4835+1_4835+11del	XP_005258040.1:n.4835+1_4835+11del
XM_005257984.1:c.4772+1_4772+11del	XP_005258041.1:n.4772+1_4772+11del
XM_006721922.1:c.4865+1_4865+11del	XP_006721985.1:n.4865+1_4865+11del
XM_006721923.2:c.4826+1_4826+11del	XP_006721986.1:n.4826+1_4826+11del
XM_006721924.1:c.4865+1_4865+11del	XP_006721987.1:n.4865+1_4865+11del
XM_006721925.1:c.4802+1_4802+11del	XP_006721988.1:n.4802+1_4802+11del
XM_006721926.2:c.4865+1_4865+11del	XP_006721989.1:n.4865+1_4865+11del
XM_006721927.1:c.4865+1_4865+11del	XP_006721990.1:n.4865+1_4865+11del
XM_006721928.2:c.4865+1_4865+11del	XP_006721991.1:n.4865+1_4865+11del
XM_011524852.1:c.4862+1_4862+11del	XP_011523154.1:n.4862+1_4862+11del
XM_011524853.1:c.4826+1_4826+11del	XP_011523155.1:n.4826+1_4826+11del
XM_011524854.1:c.4826+1_4826+11del	XP_011523156.1:n.4826+1_4826+11del
XM_011524855.1:c.4826+1_4826+11del	XP_011523157.1:n.4826+1_4826+11del
XM_011524856.1:c.4826+1_4826+11del	XP_011523158.1:n.4826+1_4826+11del
XM_011524857.1:c.4865+1_4865+11del	XP_011523159.1:n.4865+1_4865+11del
NM_001042492.3:c.4835+1_4835+11del MANE Select	NP_001035957.1:n.4835+1_4835+11del