Canonical Allele Identifier: CA2695225402

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31261779del , CM000679.2:g.31261779del	GRCh38
NC_000017.10:g.29588797del , CM000679.1:g.29588797del	GRCh37
NC_000017.9:g.26612923del	NCBI36
NG_009018.1:g.171803del , LRG_214:g.171803del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581113.7:c.448del	ENSP00000492721.2:p.Gln150ArgfsTer14
ENST00000696138.1:c.4628del	ENSP00000512431.1:p.Pro1543GlnfsTer25
ENST00000696140.1:n.752del
ENST00000696141.1:c.637del
ENST00000687863.1:n.1291del
ENST00000691014.1:c.4676del	ENSP00000510595.1:p.Pro1559GlnfsTer25
ENST00000358273.9:c.4646del MANE Select	ENSP00000351015.4:p.Pro1549GlnfsTer25
ENST00000356175.7:c.4583del	ENSP00000348498.3:p.Pro1528GlnfsTer25
ENST00000358273.8:c.4646del	ENSP00000351015.4:p.Pro1549GlnfsTer25
ENST00000456735.6:c.3581del	ENSP00000389907.2:p.Pro1194GlnfsTer25
ENST00000466819.5:c.1162del
ENST00000479614.1:c.1099del
ENST00000493220.5:n.3119del
ENST00000579081.5:c.4685del	ENSP00000462408.1:p.Pro1562GlnfsTer25
NM_000267.3:c.4583del , LRG_214t1:c.4583del	NP_000258.1:p.Pro1528GlnfsTer25
NM_001042492.2:c.4646del , LRG_214t2:c.4646del	NP_001035957.1:p.Pro1549GlnfsTer25
XM_005257983.1:c.4646del	XP_005258040.1:p.Pro1549GlnfsTer25
XM_005257984.1:c.4583del	XP_005258041.1:p.Pro1528GlnfsTer25
XM_006721922.1:c.4676del	XP_006721985.1:p.Pro1559GlnfsTer25
XM_006721923.2:c.4637del	XP_006721986.1:p.Pro1546GlnfsTer25
XM_006721924.1:c.4676del	XP_006721987.1:p.Pro1559GlnfsTer25
XM_006721925.1:c.4613del	XP_006721988.1:p.Pro1538GlnfsTer25
XM_006721926.2:c.4676del	XP_006721989.1:p.Pro1559GlnfsTer25
XM_006721927.1:c.4676del	XP_006721990.1:p.Pro1559GlnfsTer25
XM_006721928.2:c.4676del	XP_006721991.1:p.Pro1559GlnfsTer25
XM_011524852.1:c.4673del	XP_011523154.1:p.Pro1558GlnfsTer25
XM_011524853.1:c.4637del	XP_011523155.1:p.Pro1546GlnfsTer25
XM_011524854.1:c.4637del	XP_011523156.1:p.Pro1546GlnfsTer25
XM_011524855.1:c.4637del	XP_011523157.1:p.Pro1546GlnfsTer25
XM_011524856.1:c.4637del	XP_011523158.1:p.Pro1546GlnfsTer25
XM_011524857.1:c.4676del	XP_011523159.1:p.Pro1559GlnfsTer25
NM_001042492.3:c.4646del MANE Select	NP_001035957.1:p.Pro1549GlnfsTer25