Canonical Allele Identifier: CA2255602874
Gene: NF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31338120_31338121delinsTA , CM000679.2:g.31338120_31338121delinsTA GRCh38
NC_000017.10:g.29665138_29665139delinsTA , CM000679.1:g.29665138_29665139delinsTA GRCh37
NC_000017.9:g.26689264_26689265delinsTA NCBI36
NG_009018.1:g.248144_248145delinsTA , LRG_214:g.248144_248145delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.6782_6783delinsTA ENSP00000512431.1:p.Ile2261=
ENST00000684826.1:c.1364_1365delinsTA ENSP00000509994.1:p.Ile455=
ENST00000684998.1:n.2058_2059delinsTA
ENST00000687027.1:c.956_957delinsTA ENSP00000508715.1:p.Ile319=
ENST00000687863.1:n.3445_3446delinsTA
ENST00000691014.1:c.6830_6831delinsTA ENSP00000510595.1:p.Ile2277=
ENST00000693617.1:c.1364_1365delinsTA ENSP00000510031.1:p.Ile455=
ENST00000358273.9:c.6800_6801delinsTA MANE Select ENSP00000351015.4:p.Ile2267=
ENST00000356175.7:c.6737_6738delinsTA ENSP00000348498.3:p.Ile2246=
ENST00000358273.8:c.6800_6801delinsTA ENSP00000351015.4:p.Ile2267=
ENST00000456735.6:c.5735_5736delinsTA ENSP00000389907.2:p.Ile1912=
ENST00000471572.6:c.183_184delinsTA
ENST00000579081.5:c.6936_6937delinsTA ENSP00000462408.1:n.6936_6937delinsTA
ENST00000581790.5:c.64+240_64+241delinsTA
ENST00000584328.1:n.214_215delinsTA
NM_000267.3:c.6737_6738delinsTA , LRG_214t1:c.6737_6738delinsTA NP_000258.1:p.Ile2246=
NM_001042492.2:c.6800_6801delinsTA , LRG_214t2:c.6800_6801delinsTA NP_001035957.1:p.Ile2267=
XM_005257983.1:c.6800_6801delinsTA XP_005258040.1:p.Ile2267=
XM_005257984.1:c.6737_6738delinsTA XP_005258041.1:p.Ile2246=
XM_006721922.1:c.6830_6831delinsTA XP_006721985.1:p.Ile2277=
XM_006721923.2:c.6791_6792delinsTA XP_006721986.1:p.Ile2264=
XM_006721924.1:c.6830_6831delinsTA XP_006721987.1:p.Ile2277=
XM_006721925.1:c.6767_6768delinsTA XP_006721988.1:p.Ile2256=
XM_006721926.2:c.6830_6831delinsTA XP_006721989.1:p.Ile2277=
XM_006721927.1:c.6830_6831delinsTA XP_006721990.1:p.Ile2277=
XM_011524852.1:c.6827_6828delinsTA XP_011523154.1:p.Ile2276=
XM_011524853.1:c.6791_6792delinsTA XP_011523155.1:p.Ile2264=
XM_011524854.1:c.6791_6792delinsTA XP_011523156.1:p.Ile2264=
XM_011524855.1:c.6791_6792delinsTA XP_011523157.1:p.Ile2264=
XM_011524856.1:c.6791_6792delinsTA XP_011523158.1:p.Ile2264=
XM_011524857.1:c.6830_6831delinsTA XP_011523159.1:p.Ile2277=
NM_001042492.3:c.6800_6801delinsTA MANE Select NP_001035957.1:p.Ile2267=