Canonical Allele Identifier: CA2841510091
Gene: NF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31265362_31265363insAAA , CM000679.2:g.31265362_31265363insAAA GRCh38
NC_000017.10:g.29592380_29592381insAAA , CM000679.1:g.29592380_29592381insAAA GRCh37
NC_000017.9:g.26616506_26616507insAAA NCBI36
NG_009018.1:g.175386_175387insAAA , LRG_214:g.175386_175387insAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000581113.7:c.637+23_637+24insAAA ENSP00000492721.2:n.637+23_637+24insAAA
ENST00000696138.1:c.4817+23_4817+24insAAA ENSP00000512431.1:n.4817+23_4817+24insAAA
ENST00000696140.1:n.941+23_941+24insAAA
ENST00000696141.1:c.826+23_826+24insAAA
ENST00000687863.1:n.1480+23_1480+24insAAA
ENST00000691014.1:c.4865+23_4865+24insAAA ENSP00000510595.1:n.4865+23_4865+24insAAA
ENST00000358273.9:c.4835+23_4835+24insAAA MANE Select ENSP00000351015.4:n.4835+23_4835+24insAAA
ENST00000356175.7:c.4772+23_4772+24insAAA ENSP00000348498.3:n.4772+23_4772+24insAAA
ENST00000358273.8:c.4835+23_4835+24insAAA ENSP00000351015.4:n.4835+23_4835+24insAAA
ENST00000456735.6:c.3770+23_3770+24insAAA ENSP00000389907.2:n.3770+23_3770+24insAAA
ENST00000493220.5:n.3308+23_3308+24insAAA
ENST00000579081.5:c.4874+23_4874+24insAAA ENSP00000462408.1:n.4874+23_4874+24insAAA
NM_000267.3:c.4772+23_4772+24insAAA , LRG_214t1:c.4772+23_4772+24insAAA NP_000258.1:n.4772+23_4772+24insAAA
NM_001042492.2:c.4835+23_4835+24insAAA , LRG_214t2:c.4835+23_4835+24insAAA NP_001035957.1:n.4835+23_4835+24insAAA
XM_005257983.1:c.4835+23_4835+24insAAA XP_005258040.1:n.4835+23_4835+24insAAA
XM_005257984.1:c.4772+23_4772+24insAAA XP_005258041.1:n.4772+23_4772+24insAAA
XM_006721922.1:c.4865+23_4865+24insAAA XP_006721985.1:n.4865+23_4865+24insAAA
XM_006721923.2:c.4826+23_4826+24insAAA XP_006721986.1:n.4826+23_4826+24insAAA
XM_006721924.1:c.4865+23_4865+24insAAA XP_006721987.1:n.4865+23_4865+24insAAA
XM_006721925.1:c.4802+23_4802+24insAAA XP_006721988.1:n.4802+23_4802+24insAAA
XM_006721926.2:c.4865+23_4865+24insAAA XP_006721989.1:n.4865+23_4865+24insAAA
XM_006721927.1:c.4865+23_4865+24insAAA XP_006721990.1:n.4865+23_4865+24insAAA
XM_006721928.2:c.4865+23_4865+24insAAA XP_006721991.1:n.4865+23_4865+24insAAA
XM_011524852.1:c.4862+23_4862+24insAAA XP_011523154.1:n.4862+23_4862+24insAAA
XM_011524853.1:c.4826+23_4826+24insAAA XP_011523155.1:n.4826+23_4826+24insAAA
XM_011524854.1:c.4826+23_4826+24insAAA XP_011523156.1:n.4826+23_4826+24insAAA
XM_011524855.1:c.4826+23_4826+24insAAA XP_011523157.1:n.4826+23_4826+24insAAA
XM_011524856.1:c.4826+23_4826+24insAAA XP_011523158.1:n.4826+23_4826+24insAAA
XM_011524857.1:c.4865+23_4865+24insAAA XP_011523159.1:n.4865+23_4865+24insAAA
NM_001042492.3:c.4835+23_4835+24insAAA MANE Select NP_001035957.1:n.4835+23_4835+24insAAA