Canonical Allele Identifier: CA2255605177

Gene: NF1

Linked Data

• dbSNP Id: rs2069873770
• gnomAD v4: 17-31343245-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31343245_31343246insC , CM000679.2:g.31343245_31343246insC	GRCh38
NC_000017.10:g.29670263_29670264insC , CM000679.1:g.29670263_29670264insC	GRCh37
NC_000017.9:g.26694389_26694390insC	NCBI36
NG_009018.1:g.253269_253270insC , LRG_214:g.253269_253270insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7171+110_7171+111insC	ENSP00000512431.1:n.7171+110_7171+111insC
ENST00000684826.1:c.1753+110_1753+111insC	ENSP00000509994.1:n.1753+110_1753+111insC
ENST00000687027.1:c.1345+110_1345+111insC	ENSP00000508715.1:n.1345+110_1345+111insC
ENST00000687863.1:n.3834+110_3834+111insC
ENST00000689464.1:c.128+110_128+111insC
ENST00000691014.1:c.7219+110_7219+111insC	ENSP00000510595.1:n.7219+110_7219+111insC
ENST00000693617.1:c.1753+110_1753+111insC	ENSP00000510031.1:n.1753+110_1753+111insC
ENST00000358273.9:c.7189+110_7189+111insC MANE Select	ENSP00000351015.4:n.7189+110_7189+111insC
ENST00000356175.7:c.7126+110_7126+111insC	ENSP00000348498.3:n.7126+110_7126+111insC
ENST00000358273.8:c.7189+110_7189+111insC	ENSP00000351015.4:n.7189+110_7189+111insC
ENST00000456735.6:c.6124+110_6124+111insC	ENSP00000389907.2:n.6124+110_6124+111insC
ENST00000471572.6:c.572+110_572+111insC
ENST00000579081.5:c.7325+110_7325+111insC	ENSP00000462408.1:n.7325+110_7325+111insC
ENST00000581790.5:c.332+110_332+111insC
ENST00000582892.1:n.431+110_431+111insC
NM_000267.3:c.7126+110_7126+111insC , LRG_214t1:c.7126+110_7126+111insC	NP_000258.1:n.7126+110_7126+111insC
NM_001042492.2:c.7189+110_7189+111insC , LRG_214t2:c.7189+110_7189+111insC	NP_001035957.1:n.7189+110_7189+111insC
XM_005257983.1:c.7189+110_7189+111insC	XP_005258040.1:n.7189+110_7189+111insC
XM_005257984.1:c.7126+110_7126+111insC	XP_005258041.1:n.7126+110_7126+111insC
XM_006721922.1:c.7219+110_7219+111insC	XP_006721985.1:n.7219+110_7219+111insC
XM_006721923.2:c.7180+110_7180+111insC	XP_006721986.1:n.7180+110_7180+111insC
XM_006721924.1:c.7219+110_7219+111insC	XP_006721987.1:n.7219+110_7219+111insC
XM_006721925.1:c.7156+110_7156+111insC	XP_006721988.1:n.7156+110_7156+111insC
XM_006721926.2:c.7219+110_7219+111insC	XP_006721989.1:n.7219+110_7219+111insC
XM_006721927.1:c.7219+110_7219+111insC	XP_006721990.1:n.7219+110_7219+111insC
XM_011524852.1:c.7216+110_7216+111insC	XP_011523154.1:n.7216+110_7216+111insC
XM_011524853.1:c.7180+110_7180+111insC	XP_011523155.1:n.7180+110_7180+111insC
XM_011524854.1:c.7180+110_7180+111insC	XP_011523156.1:n.7180+110_7180+111insC
XM_011524855.1:c.7180+110_7180+111insC	XP_011523157.1:n.7180+110_7180+111insC
XM_011524856.1:c.7180+110_7180+111insC	XP_011523158.1:n.7180+110_7180+111insC
XM_011524857.1:c.7219+110_7219+111insC	XP_011523159.1:n.7219+110_7219+111insC
NM_001042492.3:c.7189+110_7189+111insC MANE Select	NP_001035957.1:n.7189+110_7189+111insC