Canonical Allele Identifier: CA399014429
Gene: NF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.31338792C>A , CM000679.2:g.31338792C>A GRCh38
NC_000017.10:g.29665810C>A , CM000679.1:g.29665810C>A GRCh37
NC_000017.9:g.26689936C>A NCBI36
NG_009018.1:g.248816C>A , LRG_214:g.248816C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696138.1:c.6890C>A ENSP00000512431.1:p.Pro2297Gln
ENST00000684826.1:c.1472C>A ENSP00000509994.1:p.Pro491Gln
ENST00000684998.1:n.2730C>A
ENST00000687027.1:c.1064C>A ENSP00000508715.1:p.Pro355Gln
ENST00000687863.1:n.3553C>A
ENST00000691014.1:c.6938C>A ENSP00000510595.1:p.Pro2313Gln
ENST00000693617.1:c.1472C>A ENSP00000510031.1:p.Pro491Gln
ENST00000358273.9:c.6908C>A MANE Select ENSP00000351015.4:p.Pro2303Gln
ENST00000356175.7:c.6845C>A ENSP00000348498.3:p.Pro2282Gln
ENST00000358273.8:c.6908C>A ENSP00000351015.4:p.Pro2303Gln
ENST00000456735.6:c.5843C>A ENSP00000389907.2:p.Pro1948Gln
ENST00000471572.6:c.291C>A
ENST00000579081.5:c.7044C>A ENSP00000462408.1:n.7044C>A
ENST00000581790.5:c.64+912C>A
ENST00000584328.1:n.322C>A
NM_000267.3:c.6845C>A , LRG_214t1:c.6845C>A NP_000258.1:p.Pro2282Gln
NM_001042492.2:c.6908C>A , LRG_214t2:c.6908C>A NP_001035957.1:p.Pro2303Gln
XM_005257983.1:c.6908C>A XP_005258040.1:p.Pro2303Gln
XM_005257984.1:c.6845C>A XP_005258041.1:p.Pro2282Gln
XM_006721922.1:c.6938C>A XP_006721985.1:p.Pro2313Gln
XM_006721923.2:c.6899C>A XP_006721986.1:p.Pro2300Gln
XM_006721924.1:c.6938C>A XP_006721987.1:p.Pro2313Gln
XM_006721925.1:c.6875C>A XP_006721988.1:p.Pro2292Gln
XM_006721926.2:c.6938C>A XP_006721989.1:p.Pro2313Gln
XM_006721927.1:c.6938C>A XP_006721990.1:p.Pro2313Gln
XM_011524852.1:c.6935C>A XP_011523154.1:p.Pro2312Gln
XM_011524853.1:c.6899C>A XP_011523155.1:p.Pro2300Gln
XM_011524854.1:c.6899C>A XP_011523156.1:p.Pro2300Gln
XM_011524855.1:c.6899C>A XP_011523157.1:p.Pro2300Gln
XM_011524856.1:c.6899C>A XP_011523158.1:p.Pro2300Gln
XM_011524857.1:c.6938C>A XP_011523159.1:p.Pro2313Gln
NM_001042492.3:c.6908C>A MANE Select NP_001035957.1:p.Pro2303Gln