Canonical Allele Identifier: CA399015528
Gene: NF1 HGNC NCBI

Linked Data

dbSNP Id: rs2151564973

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31343021G>C , CM000679.2:g.31343021G>C GRCh38
NC_000017.10:g.29670039G>C , CM000679.1:g.29670039G>C GRCh37
NC_000017.9:g.26694165G>C NCBI36
NG_009018.1:g.253045G>C , LRG_214:g.253045G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.7057G>C ENSP00000512431.1:p.Val2353Leu
ENST00000684826.1:c.1639G>C ENSP00000509994.1:p.Val547Leu
ENST00000687027.1:c.1231G>C ENSP00000508715.1:p.Val411Leu
ENST00000687863.1:n.3720G>C
ENST00000689464.1:c.14G>C
ENST00000691014.1:c.7105G>C ENSP00000510595.1:p.Val2369Leu
ENST00000693617.1:c.1639G>C ENSP00000510031.1:p.Val547Leu
ENST00000358273.9:c.7075G>C MANE Select ENSP00000351015.4:p.Val2359Leu
ENST00000356175.7:c.7012G>C ENSP00000348498.3:p.Val2338Leu
ENST00000358273.8:c.7075G>C ENSP00000351015.4:p.Val2359Leu
ENST00000456735.6:c.6010G>C ENSP00000389907.2:p.Val2004Leu
ENST00000471572.6:c.458G>C
ENST00000579081.5:c.7211G>C ENSP00000462408.1:n.7211G>C
ENST00000581790.5:c.218G>C
ENST00000582892.1:n.317G>C
ENST00000584328.1:n.489G>C
NM_000267.3:c.7012G>C , LRG_214t1:c.7012G>C NP_000258.1:p.Val2338Leu
NM_001042492.2:c.7075G>C , LRG_214t2:c.7075G>C NP_001035957.1:p.Val2359Leu
XM_005257983.1:c.7075G>C XP_005258040.1:p.Val2359Leu
XM_005257984.1:c.7012G>C XP_005258041.1:p.Val2338Leu
XM_006721922.1:c.7105G>C XP_006721985.1:p.Val2369Leu
XM_006721923.2:c.7066G>C XP_006721986.1:p.Val2356Leu
XM_006721924.1:c.7105G>C XP_006721987.1:p.Val2369Leu
XM_006721925.1:c.7042G>C XP_006721988.1:p.Val2348Leu
XM_006721926.2:c.7105G>C XP_006721989.1:p.Val2369Leu
XM_006721927.1:c.7105G>C XP_006721990.1:p.Val2369Leu
XM_011524852.1:c.7102G>C XP_011523154.1:p.Val2368Leu
XM_011524853.1:c.7066G>C XP_011523155.1:p.Val2356Leu
XM_011524854.1:c.7066G>C XP_011523156.1:p.Val2356Leu
XM_011524855.1:c.7066G>C XP_011523157.1:p.Val2356Leu
XM_011524856.1:c.7066G>C XP_011523158.1:p.Val2356Leu
XM_011524857.1:c.7105G>C XP_011523159.1:p.Val2369Leu
NM_001042492.3:c.7075G>C MANE Select NP_001035957.1:p.Val2359Leu