Canonical Allele Identifier: CA2255573298
Gene: NF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31258331_31258332delinsTC , CM000679.2:g.31258331_31258332delinsTC GRCh38
NC_000017.10:g.29585349_29585350delinsTC , CM000679.1:g.29585349_29585350delinsTC GRCh37
NC_000017.9:g.26609475_26609476delinsTC NCBI36
NG_009018.1:g.168355_168356delinsTC , LRG_214:g.168355_168356delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.4156-13_4156-12delinsTC ENSP00000512431.1:n.4156-13_4156-12delinsTC
ENST00000696140.1:n.280-13_280-12delinsTC
ENST00000696141.1:c.165-13_165-12delinsTC
ENST00000687863.1:n.819-13_819-12delinsTC
ENST00000691014.1:c.4204-13_4204-12delinsTC ENSP00000510595.1:n.4204-13_4204-12delinsTC
ENST00000691649.1:n.133_134delinsTC
ENST00000358273.9:c.4174-13_4174-12delinsTC MANE Select ENSP00000351015.4:n.4174-13_4174-12delinsTC
ENST00000356175.7:c.4111-13_4111-12delinsTC ENSP00000348498.3:n.4111-13_4111-12delinsTC
ENST00000358273.8:c.4174-13_4174-12delinsTC ENSP00000351015.4:n.4174-13_4174-12delinsTC
ENST00000456735.6:c.3109-13_3109-12delinsTC ENSP00000389907.2:n.3109-13_3109-12delinsTC
ENST00000466819.5:c.690-13_690-12delinsTC
ENST00000479614.1:c.627-13_627-12delinsTC
ENST00000493220.5:n.2647-13_2647-12delinsTC
ENST00000579081.5:c.4213-13_4213-12delinsTC ENSP00000462408.1:n.4213-13_4213-12delinsTC
NM_000267.3:c.4111-13_4111-12delinsTC , LRG_214t1:c.4111-13_4111-12delinsTC NP_000258.1:n.4111-13_4111-12delinsTC
NM_001042492.2:c.4174-13_4174-12delinsTC , LRG_214t2:c.4174-13_4174-12delinsTC NP_001035957.1:n.4174-13_4174-12delinsTC
XM_005257983.1:c.4174-13_4174-12delinsTC XP_005258040.1:n.4174-13_4174-12delinsTC
XM_005257984.1:c.4111-13_4111-12delinsTC XP_005258041.1:n.4111-13_4111-12delinsTC
XM_006721922.1:c.4204-13_4204-12delinsTC XP_006721985.1:n.4204-13_4204-12delinsTC
XM_006721923.2:c.4165-13_4165-12delinsTC XP_006721986.1:n.4165-13_4165-12delinsTC
XM_006721924.1:c.4204-13_4204-12delinsTC XP_006721987.1:n.4204-13_4204-12delinsTC
XM_006721925.1:c.4141-13_4141-12delinsTC XP_006721988.1:n.4141-13_4141-12delinsTC
XM_006721926.2:c.4204-13_4204-12delinsTC XP_006721989.1:n.4204-13_4204-12delinsTC
XM_006721927.1:c.4204-13_4204-12delinsTC XP_006721990.1:n.4204-13_4204-12delinsTC
XM_006721928.2:c.4204-13_4204-12delinsTC XP_006721991.1:n.4204-13_4204-12delinsTC
XM_011524852.1:c.4201-13_4201-12delinsTC XP_011523154.1:n.4201-13_4201-12delinsTC
XM_011524853.1:c.4165-13_4165-12delinsTC XP_011523155.1:n.4165-13_4165-12delinsTC
XM_011524854.1:c.4165-13_4165-12delinsTC XP_011523156.1:n.4165-13_4165-12delinsTC
XM_011524855.1:c.4165-13_4165-12delinsTC XP_011523157.1:n.4165-13_4165-12delinsTC
XM_011524856.1:c.4165-13_4165-12delinsTC XP_011523158.1:n.4165-13_4165-12delinsTC
XM_011524857.1:c.4204-13_4204-12delinsTC XP_011523159.1:n.4204-13_4204-12delinsTC
NM_001042492.3:c.4174-13_4174-12delinsTC MANE Select NP_001035957.1:n.4174-13_4174-12delinsTC