Canonical Allele Identifier: CA351509414
Gene: RAF1 HGNC NCBI

Linked Data

dbSNP Id: rs2125380799

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600252G>T , CM000665.2:g.12600252G>T GRCh38
NC_000003.11:g.12641751G>T , CM000665.1:g.12641751G>T GRCh37
NC_000003.10:g.12616751G>T NCBI36
NG_007467.1:g.68928C>A , LRG_413:g.68928C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*555C>A ENSP00000401088.1:n.*555C>A
ENST00000432427.3:c.210C>A
ENST00000465826.6:n.481C>A
ENST00000491290.2:n.1267C>A
ENST00000684903.1:c.*567C>A ENSP00000508612.1:n.*567C>A
ENST00000685348.1:c.*567C>A ENSP00000510285.1:n.*567C>A
ENST00000685437.1:c.791C>A ENSP00000508794.1:p.Pro264His
ENST00000685438.1:n.654C>A
ENST00000685653.1:c.890C>A ENSP00000509968.1:p.Pro297His
ENST00000685738.1:c.890C>A ENSP00000510156.1:p.Pro297His
ENST00000686409.1:n.1598C>A
ENST00000686455.1:n.1253C>A
ENST00000686479.1:n.1261C>A
ENST00000686762.1:c.890C>A ENSP00000509767.1:p.Pro297His
ENST00000687257.1:n.1126C>A
ENST00000687326.1:c.890C>A ENSP00000509665.1:p.Pro297His
ENST00000687486.1:c.182+136C>A
ENST00000687505.1:n.1008C>A
ENST00000687923.1:c.791C>A ENSP00000510255.1:p.Pro264His
ENST00000687940.1:n.1267C>A
ENST00000688269.1:n.1486C>A
ENST00000688326.1:c.210C>A
ENST00000688444.1:n.1216C>A
ENST00000688543.1:c.791C>A ENSP00000509612.1:p.Pro264His
ENST00000688625.1:c.*468C>A ENSP00000509522.1:n.*468C>A
ENST00000688803.1:n.1121C>A
ENST00000689097.1:c.*567C>A ENSP00000509756.1:n.*567C>A
ENST00000689389.1:c.890C>A ENSP00000510213.1:p.Pro297His
ENST00000689418.1:c.*567C>A ENSP00000509467.1:n.*567C>A
ENST00000689481.1:c.*567C>A ENSP00000510248.1:n.*567C>A
ENST00000689540.1:n.1040C>A
ENST00000689876.1:c.890C>A ENSP00000508535.1:p.Pro297His
ENST00000689914.1:c.890C>A ENSP00000509847.1:p.Pro297His
ENST00000690397.1:c.779C>A ENSP00000508730.1:p.Pro260His
ENST00000690460.1:c.878C>A ENSP00000509106.1:p.Pro293His
ENST00000690625.1:n.1193C>A
ENST00000691268.1:c.317C>A
ENST00000691396.1:c.*683C>A ENSP00000510712.1:n.*683C>A
ENST00000691724.1:c.890C>A ENSP00000509255.1:p.Pro297His
ENST00000691779.1:c.*468C>A ENSP00000508592.1:n.*468C>A
ENST00000691899.1:c.890C>A ENSP00000508763.1:p.Pro297His
ENST00000692069.1:n.1113C>A
ENST00000692093.1:c.791C>A ENSP00000509669.1:p.Pro264His
ENST00000692311.1:n.1371C>A
ENST00000692558.1:n.1255C>A
ENST00000692773.1:c.*627C>A ENSP00000509055.1:n.*627C>A
ENST00000692830.1:c.*635C>A ENSP00000509461.1:n.*635C>A
ENST00000693069.1:c.791C>A ENSP00000510072.1:p.Pro264His
ENST00000693312.1:c.665C>A ENSP00000508686.1:p.Pro222His
ENST00000693664.1:c.890C>A ENSP00000509614.1:p.Pro297His
ENST00000693705.1:c.*567C>A ENSP00000510697.1:n.*567C>A
ENST00000251849.9:c.890C>A MANE Select ENSP00000251849.4:p.Pro297His
ENST00000442415.7:c.950C>A ENSP00000401888.2:p.Pro317His
ENST00000251849.8:c.890C>A ENSP00000251849.4:p.Pro297His
ENST00000423275.5:c.*567C>A ENSP00000401088.1:n.*567C>A
ENST00000432427.2:c.527C>A ENSP00000398591.2:p.Pro176His
ENST00000442415.6:c.950C>A ENSP00000401888.2:p.Pro317His
ENST00000465826.5:n.134C>A
ENST00000491290.1:n.519C>A
NM_002880.3:c.890C>A , LRG_413t1:c.890C>A NP_002871.1:p.Pro297His
XM_005265355.1:c.890C>A XP_005265412.1:p.Pro297His
XM_005265357.1:c.791C>A XP_005265414.1:p.Pro264His
XM_005265358.3:c.647C>A XP_005265415.1:p.Pro216His
XM_005265359.3:c.548C>A XP_005265416.1:p.Pro183His
XM_005265360.1:c.890C>A XP_005265417.1:p.Pro297His
XM_011533974.1:c.890C>A XP_011532276.1:p.Pro297His
XM_011533975.1:c.647C>A XP_011532277.1:p.Pro216His
NM_001354689.1:c.950C>A NP_001341618.1:p.Pro317His
NM_001354690.1:c.890C>A NP_001341619.1:p.Pro297His
NM_001354691.1:c.647C>A NP_001341620.1:p.Pro216His
NM_001354692.1:c.647C>A NP_001341621.1:p.Pro216His
NM_001354693.1:c.791C>A NP_001341622.1:p.Pro264His
NM_001354694.1:c.707C>A NP_001341623.1:p.Pro236His
NM_001354695.1:c.548C>A NP_001341624.1:p.Pro183His
NR_148940.1:n.1305C>A
NR_148941.1:n.1305C>A
NR_148942.1:n.1305C>A
XM_011533974.3:c.890C>A XP_011532276.1:p.Pro297His
XM_017006966.1:c.791C>A XP_016862455.1:p.Pro264His
XR_001740227.1:n.1122C>A
NM_001354689.3:c.950C>A NP_001341618.1:p.Pro317His
NM_001354690.2:c.890C>A NP_001341619.1:p.Pro297His
NM_001354691.2:c.647C>A NP_001341620.1:p.Pro216His
NM_001354692.2:c.647C>A NP_001341621.1:p.Pro216His
NM_001354693.2:c.791C>A NP_001341622.1:p.Pro264His
NM_001354694.2:c.707C>A NP_001341623.1:p.Pro236His
NM_001354695.2:c.548C>A NP_001341624.1:p.Pro183His
NR_148940.2:n.1221C>A
NR_148941.2:n.1221C>A
NR_148942.2:n.1221C>A
NM_001354690.3:c.890C>A NP_001341619.1:p.Pro297His
NM_001354691.3:c.647C>A NP_001341620.1:p.Pro216His
NM_001354692.3:c.647C>A NP_001341621.1:p.Pro216His
NM_001354693.3:c.791C>A NP_001341622.1:p.Pro264His
NM_001354694.3:c.707C>A NP_001341623.1:p.Pro236His
NM_001354695.3:c.548C>A NP_001341624.1:p.Pro183His
NM_002880.4:c.890C>A MANE Select NP_002871.1:p.Pro297His
NR_148940.3:n.1221C>A
NR_148941.3:n.1221C>A
NR_148942.3:n.1221C>A