Canonical Allele Identifier: CA164511
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141116
dbSNP Id: rs373563053

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31159036A>T , CM000679.2:g.31159036A>T GRCh38
NC_000017.10:g.29486054A>T , CM000679.1:g.29486054A>T GRCh37
NC_000017.9:g.26510180A>T NCBI36
NG_009018.1:g.69060A>T , LRG_214:g.69060A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.231A>T ENSP00000512431.1:p.Lys77Asn
ENST00000691014.1:c.231A>T ENSP00000510595.1:p.Lys77Asn
ENST00000358273.9:c.231A>T MANE Select ENSP00000351015.4:p.Lys77Asn
ENST00000356175.7:c.231A>T ENSP00000348498.3:p.Lys77Asn
ENST00000358273.8:c.231A>T ENSP00000351015.4:p.Lys77Asn
ENST00000431387.8:c.231A>T ENSP00000412921.4:p.Lys77Asn
ENST00000487476.5:n.614A>T
ENST00000489712.6:c.30A>T ENSP00000467284.1:p.Lys10Asn
ENST00000495910.6:c.113A>T
ENST00000579081.5:c.333A>T ENSP00000462408.1:p.Lys111Asn
NM_000267.3:c.231A>T , LRG_214t1:c.231A>T NP_000258.1:p.Lys77Asn
NM_001042492.2:c.231A>T , LRG_214t2:c.231A>T NP_001035957.1:p.Lys77Asn
NM_001128147.2:c.231A>T NP_001121619.1:p.Lys77Asn
XM_005257983.1:c.231A>T XP_005258040.1:p.Lys77Asn
XM_005257984.1:c.231A>T XP_005258041.1:p.Lys77Asn
XM_006721922.1:c.231A>T XP_006721985.1:p.Lys77Asn
XM_006721923.2:c.192A>T XP_006721986.1:p.Lys64Asn
XM_006721924.1:c.231A>T XP_006721987.1:p.Lys77Asn
XM_006721925.1:c.231A>T XP_006721988.1:p.Lys77Asn
XM_006721926.2:c.231A>T XP_006721989.1:p.Lys77Asn
XM_006721927.1:c.231A>T XP_006721990.1:p.Lys77Asn
XM_006721928.2:c.231A>T XP_006721991.1:p.Lys77Asn
XM_011524852.1:c.231A>T XP_011523154.1:p.Lys77Asn
XM_011524853.1:c.192A>T XP_011523155.1:p.Lys64Asn
XM_011524854.1:c.192A>T XP_011523156.1:p.Lys64Asn
XM_011524855.1:c.192A>T XP_011523157.1:p.Lys64Asn
XM_011524856.1:c.192A>T XP_011523158.1:p.Lys64Asn
XM_011524857.1:c.231A>T XP_011523159.1:p.Lys77Asn
NM_001042492.3:c.231A>T MANE Select NP_001035957.1:p.Lys77Asn
NM_001128147.3:c.231A>T NP_001121619.1:p.Lys77Asn