Canonical Allele Identifier: CA499236813
Gene: NF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.29670050A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31343032A>T , CM000679.2:g.31343032A>T GRCh38
NC_000017.10:g.29670050A>T , CM000679.1:g.29670050A>T GRCh37
NC_000017.9:g.26694176A>T NCBI36
NG_009018.1:g.253056A>T , LRG_214:g.253056A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.7068A>T ENSP00000512431.1:p.Ala2356=
ENST00000684826.1:c.1650A>T ENSP00000509994.1:p.Ala550=
ENST00000687027.1:c.1242A>T ENSP00000508715.1:p.Ala414=
ENST00000687863.1:n.3731A>T
ENST00000689464.1:c.25A>T
ENST00000691014.1:c.7116A>T ENSP00000510595.1:p.Ala2372=
ENST00000693617.1:c.1650A>T ENSP00000510031.1:p.Ala550=
ENST00000358273.9:c.7086A>T MANE Select ENSP00000351015.4:p.Ala2362=
ENST00000356175.7:c.7023A>T ENSP00000348498.3:p.Ala2341=
ENST00000358273.8:c.7086A>T ENSP00000351015.4:p.Ala2362=
ENST00000456735.6:c.6021A>T ENSP00000389907.2:p.Ala2007=
ENST00000471572.6:c.469A>T
ENST00000579081.5:c.7222A>T ENSP00000462408.1:n.7222A>T
ENST00000581790.5:c.229A>T
ENST00000582892.1:n.328A>T
ENST00000584328.1:n.500A>T
NM_000267.3:c.7023A>T , LRG_214t1:c.7023A>T NP_000258.1:p.Ala2341=
NM_001042492.2:c.7086A>T , LRG_214t2:c.7086A>T NP_001035957.1:p.Ala2362=
XM_005257983.1:c.7086A>T XP_005258040.1:p.Ala2362=
XM_005257984.1:c.7023A>T XP_005258041.1:p.Ala2341=
XM_006721922.1:c.7116A>T XP_006721985.1:p.Ala2372=
XM_006721923.2:c.7077A>T XP_006721986.1:p.Ala2359=
XM_006721924.1:c.7116A>T XP_006721987.1:p.Ala2372=
XM_006721925.1:c.7053A>T XP_006721988.1:p.Ala2351=
XM_006721926.2:c.7116A>T XP_006721989.1:p.Ala2372=
XM_006721927.1:c.7116A>T XP_006721990.1:p.Ala2372=
XM_011524852.1:c.7113A>T XP_011523154.1:p.Ala2371=
XM_011524853.1:c.7077A>T XP_011523155.1:p.Ala2359=
XM_011524854.1:c.7077A>T XP_011523156.1:p.Ala2359=
XM_011524855.1:c.7077A>T XP_011523157.1:p.Ala2359=
XM_011524856.1:c.7077A>T XP_011523158.1:p.Ala2359=
XM_011524857.1:c.7116A>T XP_011523159.1:p.Ala2372=
NM_001042492.3:c.7086A>T MANE Select NP_001035957.1:p.Ala2362=