Canonical Allele Identifier: CA499234320
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1755266
MyVariant Identifiers: chr17:g.29665724A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31338706A>G , CM000679.2:g.31338706A>G GRCh38
NC_000017.10:g.29665724A>G , CM000679.1:g.29665724A>G GRCh37
NC_000017.9:g.26689850A>G NCBI36
NG_009018.1:g.248730A>G , LRG_214:g.248730A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.6804A>G ENSP00000512431.1:p.Ala2268=
ENST00000684826.1:c.1386A>G ENSP00000509994.1:p.Ala462=
ENST00000684998.1:n.2644A>G
ENST00000687027.1:c.978A>G ENSP00000508715.1:p.Ala326=
ENST00000687863.1:n.3467A>G
ENST00000691014.1:c.6852A>G ENSP00000510595.1:p.Ala2284=
ENST00000693617.1:c.1386A>G ENSP00000510031.1:p.Ala462=
ENST00000358273.9:c.6822A>G MANE Select ENSP00000351015.4:p.Ala2274=
ENST00000356175.7:c.6759A>G ENSP00000348498.3:p.Ala2253=
ENST00000358273.8:c.6822A>G ENSP00000351015.4:p.Ala2274=
ENST00000456735.6:c.5757A>G ENSP00000389907.2:p.Ala1919=
ENST00000471572.6:c.205A>G
ENST00000579081.5:c.6958A>G ENSP00000462408.1:n.6958A>G
ENST00000581790.5:c.64+826A>G
ENST00000584328.1:n.236A>G
NM_000267.3:c.6759A>G , LRG_214t1:c.6759A>G NP_000258.1:p.Ala2253=
NM_001042492.2:c.6822A>G , LRG_214t2:c.6822A>G NP_001035957.1:p.Ala2274=
XM_005257983.1:c.6822A>G XP_005258040.1:p.Ala2274=
XM_005257984.1:c.6759A>G XP_005258041.1:p.Ala2253=
XM_006721922.1:c.6852A>G XP_006721985.1:p.Ala2284=
XM_006721923.2:c.6813A>G XP_006721986.1:p.Ala2271=
XM_006721924.1:c.6852A>G XP_006721987.1:p.Ala2284=
XM_006721925.1:c.6789A>G XP_006721988.1:p.Ala2263=
XM_006721926.2:c.6852A>G XP_006721989.1:p.Ala2284=
XM_006721927.1:c.6852A>G XP_006721990.1:p.Ala2284=
XM_011524852.1:c.6849A>G XP_011523154.1:p.Ala2283=
XM_011524853.1:c.6813A>G XP_011523155.1:p.Ala2271=
XM_011524854.1:c.6813A>G XP_011523156.1:p.Ala2271=
XM_011524855.1:c.6813A>G XP_011523157.1:p.Ala2271=
XM_011524856.1:c.6813A>G XP_011523158.1:p.Ala2271=
XM_011524857.1:c.6852A>G XP_011523159.1:p.Ala2284=
NM_001042492.3:c.6822A>G MANE Select NP_001035957.1:p.Ala2274=