Canonical Allele Identifier: CA398997509
Gene: NF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31258348T>C , CM000679.2:g.31258348T>C GRCh38
NC_000017.10:g.29585366T>C , CM000679.1:g.29585366T>C GRCh37
NC_000017.9:g.26609492T>C NCBI36
NG_009018.1:g.168372T>C , LRG_214:g.168372T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.4160T>C ENSP00000512431.1:p.Val1387Ala
ENST00000696140.1:n.284T>C
ENST00000696141.1:c.169T>C
ENST00000687863.1:n.823T>C
ENST00000691014.1:c.4208T>C ENSP00000510595.1:p.Val1403Ala
ENST00000691649.1:n.150T>C
ENST00000358273.9:c.4178T>C MANE Select ENSP00000351015.4:p.Val1393Ala
ENST00000356175.7:c.4115T>C ENSP00000348498.3:p.Val1372Ala
ENST00000358273.8:c.4178T>C ENSP00000351015.4:p.Val1393Ala
ENST00000456735.6:c.3113T>C ENSP00000389907.2:p.Val1038Ala
ENST00000466819.5:c.694T>C
ENST00000479614.1:c.631T>C
ENST00000493220.5:n.2651T>C
ENST00000579081.5:c.4217T>C ENSP00000462408.1:p.Val1406Ala
NM_000267.3:c.4115T>C , LRG_214t1:c.4115T>C NP_000258.1:p.Val1372Ala
NM_001042492.2:c.4178T>C , LRG_214t2:c.4178T>C NP_001035957.1:p.Val1393Ala
XM_005257983.1:c.4178T>C XP_005258040.1:p.Val1393Ala
XM_005257984.1:c.4115T>C XP_005258041.1:p.Val1372Ala
XM_006721922.1:c.4208T>C XP_006721985.1:p.Val1403Ala
XM_006721923.2:c.4169T>C XP_006721986.1:p.Val1390Ala
XM_006721924.1:c.4208T>C XP_006721987.1:p.Val1403Ala
XM_006721925.1:c.4145T>C XP_006721988.1:p.Val1382Ala
XM_006721926.2:c.4208T>C XP_006721989.1:p.Val1403Ala
XM_006721927.1:c.4208T>C XP_006721990.1:p.Val1403Ala
XM_006721928.2:c.4208T>C XP_006721991.1:p.Val1403Ala
XM_011524852.1:c.4205T>C XP_011523154.1:p.Val1402Ala
XM_011524853.1:c.4169T>C XP_011523155.1:p.Val1390Ala
XM_011524854.1:c.4169T>C XP_011523156.1:p.Val1390Ala
XM_011524855.1:c.4169T>C XP_011523157.1:p.Val1390Ala
XM_011524856.1:c.4169T>C XP_011523158.1:p.Val1390Ala
XM_011524857.1:c.4208T>C XP_011523159.1:p.Val1403Ala
NM_001042492.3:c.4178T>C MANE Select NP_001035957.1:p.Val1393Ala