Canonical Allele Identifier: CA398990439

Gene: NF1

Linked Data

• ClinVar Variation Id: 591153
• ClinVar RCV Id: RCV000722330 ; RCV001294488 ; RCV002343592 ; RCV003460998
• dbSNP Id: rs1567851424
• gnomAD v4: 17-31233151-G-T
• MyVariant Identifiers: chr17:g.29560169G>T (hg19) ; chr17:g.31233151G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31233151G>T , CM000679.2:g.31233151G>T	GRCh38
NC_000017.10:g.29560169G>T , CM000679.1:g.29560169G>T	GRCh37
NC_000017.9:g.26584295G>T	NCBI36
NG_009018.1:g.143175G>T , LRG_214:g.143175G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.3691G>T	ENSP00000512431.1:p.Gly1231Cys
ENST00000696139.1:c.991G>T	ENSP00000512432.1:p.Gly331Cys
ENST00000691014.1:c.3676G>T	ENSP00000510595.1:p.Gly1226Cys
ENST00000693210.1:n.372G>T
ENST00000358273.9:c.3646G>T MANE Select	ENSP00000351015.4:p.Gly1216Cys
ENST00000356175.7:c.3646G>T	ENSP00000348498.3:p.Gly1216Cys
ENST00000358273.8:c.3646G>T	ENSP00000351015.4:p.Gly1216Cys
ENST00000456735.6:c.2644G>T	ENSP00000389907.2:p.Gly882Cys
ENST00000466819.5:c.122G>T
ENST00000479614.1:c.122G>T
ENST00000493220.5:n.2182G>T
ENST00000495910.6:c.3421G>T
ENST00000579081.5:c.3748G>T	ENSP00000462408.1:p.Gly1250Cys
NM_000267.3:c.3646G>T , LRG_214t1:c.3646G>T	NP_000258.1:p.Gly1216Cys
NM_001042492.2:c.3646G>T , LRG_214t2:c.3646G>T	NP_001035957.1:p.Gly1216Cys
XM_005257983.1:c.3646G>T	XP_005258040.1:p.Gly1216Cys
XM_005257984.1:c.3646G>T	XP_005258041.1:p.Gly1216Cys
XM_006721922.1:c.3676G>T	XP_006721985.1:p.Gly1226Cys
XM_006721923.2:c.3637G>T	XP_006721986.1:p.Gly1213Cys
XM_006721924.1:c.3676G>T	XP_006721987.1:p.Gly1226Cys
XM_006721925.1:c.3676G>T	XP_006721988.1:p.Gly1226Cys
XM_006721926.2:c.3676G>T	XP_006721989.1:p.Gly1226Cys
XM_006721927.1:c.3676G>T	XP_006721990.1:p.Gly1226Cys
XM_006721928.2:c.3676G>T	XP_006721991.1:p.Gly1226Cys
XM_011524852.1:c.3673G>T	XP_011523154.1:p.Gly1225Cys
XM_011524853.1:c.3637G>T	XP_011523155.1:p.Gly1213Cys
XM_011524854.1:c.3637G>T	XP_011523156.1:p.Gly1213Cys
XM_011524855.1:c.3637G>T	XP_011523157.1:p.Gly1213Cys
XM_011524856.1:c.3637G>T	XP_011523158.1:p.Gly1213Cys
XM_011524857.1:c.3676G>T	XP_011523159.1:p.Gly1226Cys
NM_001042492.3:c.3646G>T MANE Select	NP_001035957.1:p.Gly1216Cys