Canonical Allele Identifier: CA399001345

Gene: NF1

Linked Data

• ClinVar Variation Id: 825145
• ClinVar RCV Id: RCV002319368
• dbSNP Id: rs199474766
• MyVariant Identifiers: chr17:g.29592335A>T (hg19) ; chr17:g.31265317A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31265317A>T , CM000679.2:g.31265317A>T	GRCh38
NC_000017.10:g.29592335A>T , CM000679.1:g.29592335A>T	GRCh37
NC_000017.9:g.26616461A>T	NCBI36
NG_009018.1:g.175341A>T , LRG_214:g.175341A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581113.7:c.615A>T	ENSP00000492721.2:n.615A>T
ENST00000696138.1:c.4795A>T	ENSP00000512431.1:p.Ile1599Phe
ENST00000696140.1:n.919A>T
ENST00000696141.1:c.804A>T
ENST00000687863.1:n.1458A>T
ENST00000691014.1:c.4843A>T	ENSP00000510595.1:p.Ile1615Phe
ENST00000358273.9:c.4813A>T MANE Select	ENSP00000351015.4:p.Ile1605Phe
ENST00000356175.7:c.4750A>T	ENSP00000348498.3:p.Ile1584Phe
ENST00000358273.8:c.4813A>T	ENSP00000351015.4:p.Ile1605Phe
ENST00000456735.6:c.3748A>T	ENSP00000389907.2:p.Ile1250Phe
ENST00000493220.5:n.3286A>T
ENST00000579081.5:c.4852A>T	ENSP00000462408.1:p.Ile1618Phe
NM_000267.3:c.4750A>T , LRG_214t1:c.4750A>T	NP_000258.1:p.Ile1584Phe
NM_001042492.2:c.4813A>T , LRG_214t2:c.4813A>T	NP_001035957.1:p.Ile1605Phe
XM_005257983.1:c.4813A>T	XP_005258040.1:p.Ile1605Phe
XM_005257984.1:c.4750A>T	XP_005258041.1:p.Ile1584Phe
XM_006721922.1:c.4843A>T	XP_006721985.1:p.Ile1615Phe
XM_006721923.2:c.4804A>T	XP_006721986.1:p.Ile1602Phe
XM_006721924.1:c.4843A>T	XP_006721987.1:p.Ile1615Phe
XM_006721925.1:c.4780A>T	XP_006721988.1:p.Ile1594Phe
XM_006721926.2:c.4843A>T	XP_006721989.1:p.Ile1615Phe
XM_006721927.1:c.4843A>T	XP_006721990.1:p.Ile1615Phe
XM_006721928.2:c.4843A>T	XP_006721991.1:p.Ile1615Phe
XM_011524852.1:c.4840A>T	XP_011523154.1:p.Ile1614Phe
XM_011524853.1:c.4804A>T	XP_011523155.1:p.Ile1602Phe
XM_011524854.1:c.4804A>T	XP_011523156.1:p.Ile1602Phe
XM_011524855.1:c.4804A>T	XP_011523157.1:p.Ile1602Phe
XM_011524856.1:c.4804A>T	XP_011523158.1:p.Ile1602Phe
XM_011524857.1:c.4843A>T	XP_011523159.1:p.Ile1615Phe
NM_001042492.3:c.4813A>T MANE Select	NP_001035957.1:p.Ile1605Phe