Canonical Allele Identifier: CA2664506799

Linked Data

dbSNP Id: rs2125315024
gnomAD v4: 3-12584449-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584449C>T , CM000665.2:g.12584449C>T GRCh38
NC_000003.11:g.12625948C>T , CM000665.1:g.12625948C>T GRCh37
NC_000003.10:g.12600948C>T NCBI36
NG_007467.1:g.84731G>A , LRG_413:g.84731G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1677G>A (RAF1) ENSP00000401088.1:n.*1677G>A
ENST00000432427.3:c.1329G>A (RAF1)
ENST00000460610.2:n.6324G>A (RAF1)
ENST00000471449.2:n.822G>A (RAF1)
ENST00000475353.2:n.4292G>A (RAF1)
ENST00000684903.1:c.*1689G>A (RAF1) ENSP00000508612.1:n.*1689G>A
ENST00000685348.1:c.*1723G>A (RAF1) ENSP00000510285.1:n.*1723G>A
ENST00000685437.1:c.*65G>A (RAF1) ENSP00000508794.1:n.*65G>A
ENST00000685653.1:c.*65G>A (RAF1) ENSP00000509968.1:n.*65G>A
ENST00000685697.1:n.2747G>A (RAF1)
ENST00000685738.1:c.*976G>A (RAF1) ENSP00000510156.1:n.*976G>A
ENST00000686409.1:n.5421G>A (RAF1)
ENST00000686455.1:n.4733G>A (RAF1)
ENST00000686762.1:c.*571G>A (RAF1) ENSP00000509767.1:n.*571G>A
ENST00000687257.1:n.4466G>A (RAF1)
ENST00000687326.1:c.*3304G>A (RAF1) ENSP00000509665.1:n.*3304G>A
ENST00000687505.1:n.2130G>A (RAF1)
ENST00000687923.1:c.*65G>A (RAF1) ENSP00000510255.1:n.*65G>A
ENST00000688269.1:n.2608G>A (RAF1)
ENST00000688444.1:n.4129G>A (RAF1)
ENST00000688543.1:c.*65G>A (RAF1) ENSP00000509612.1:n.*65G>A
ENST00000688625.1:c.*3381G>A (RAF1) ENSP00000509522.1:n.*3381G>A
ENST00000688803.1:n.3440G>A (RAF1)
ENST00000689097.1:c.*1689G>A (RAF1) ENSP00000509756.1:n.*1689G>A
ENST00000689389.1:c.*65G>A (RAF1) ENSP00000510213.1:n.*65G>A
ENST00000689418.1:c.*3907G>A (RAF1) ENSP00000509467.1:n.*3907G>A
ENST00000689540.1:n.4380G>A (RAF1)
ENST00000689876.1:c.*561G>A (RAF1) ENSP00000508535.1:n.*561G>A
ENST00000689914.1:c.*946G>A (RAF1) ENSP00000509847.1:n.*946G>A
ENST00000690397.1:c.*65G>A (RAF1) ENSP00000508730.1:n.*65G>A
ENST00000690460.1:c.*65G>A (RAF1) ENSP00000509106.1:n.*65G>A
ENST00000690585.1:c.738G>A (RAF1)
ENST00000690625.1:n.3048G>A (RAF1)
ENST00000691396.1:c.*1884G>A (RAF1) ENSP00000510712.1:n.*1884G>A
ENST00000691643.1:n.3065G>A (RAF1)
ENST00000691724.1:c.*969G>A (RAF1) ENSP00000509255.1:n.*969G>A
ENST00000691779.1:c.*1590G>A (RAF1) ENSP00000508592.1:n.*1590G>A
ENST00000691888.1:c.886G>A (RAF1)
ENST00000691899.1:c.*65G>A (RAF1) ENSP00000508763.1:n.*65G>A
ENST00000692069.1:n.4936G>A (RAF1)
ENST00000692093.1:c.*65G>A (RAF1) ENSP00000509669.1:n.*65G>A
ENST00000692311.1:n.2836G>A (RAF1)
ENST00000692558.1:n.4595G>A (RAF1)
ENST00000692773.1:c.*1749G>A (RAF1) ENSP00000509055.1:n.*1749G>A
ENST00000692830.1:c.*1757G>A (RAF1) ENSP00000509461.1:n.*1757G>A
ENST00000693312.1:c.*65G>A (RAF1) ENSP00000508686.1:n.*65G>A
ENST00000693664.1:c.*463G>A (RAF1) ENSP00000509614.1:n.*463G>A
ENST00000693705.1:c.*1391G>A (RAF1) ENSP00000510697.1:n.*1391G>A
ENST00000251849.9:c.*65G>A (RAF1) MANE Select ENSP00000251849.4:n.*65G>A
ENST00000442415.7:c.*65G>A (RAF1) ENSP00000401888.2:n.*65G>A
ENST00000676541.1:c.*2196C>T (MKRN2) ENSP00000503730.1:n.*2196C>T
ENST00000677142.1:c.*2196C>T (MKRN2) ENSP00000504455.1:n.*2196C>T
ENST00000677816.1:c.*751C>T (MKRN2) ENSP00000502893.1:n.*751C>T
ENST00000677941.1:n.2259C>T (MKRN2)
ENST00000251849.8:c.*65G>A (RAF1) ENSP00000251849.4:n.*65G>A
ENST00000423275.5:c.*1689G>A (RAF1) ENSP00000401088.1:n.*1689G>A
ENST00000432427.2:c.1649G>A (RAF1) ENSP00000398591.2:n.1649G>A
ENST00000442415.6:c.*65G>A (RAF1) ENSP00000401888.2:n.*65G>A
ENST00000471449.1:n.701G>A (RAF1)
NM_002880.3:c.*65G>A , LRG_413t1:c.*65G>A (RAF1) NP_002871.1:n.*65G>A
XM_005265355.1:c.*65G>A (RAF1) XP_005265412.1:n.*65G>A
XM_005265357.1:c.*65G>A (RAF1) XP_005265414.1:n.*65G>A
XM_005265358.3:c.*65G>A (RAF1) XP_005265415.1:n.*65G>A
XM_005265359.3:c.*65G>A (RAF1) XP_005265416.1:n.*65G>A
XM_011533974.1:c.*65G>A (RAF1) XP_011532276.1:n.*65G>A
XM_011533975.1:c.*65G>A (RAF1) XP_011532277.1:n.*65G>A
NM_001354689.1:c.*65G>A (RAF1) NP_001341618.1:n.*65G>A
NM_001354690.1:c.*65G>A (RAF1) NP_001341619.1:n.*65G>A
NM_001354691.1:c.*65G>A (RAF1) NP_001341620.1:n.*65G>A
NM_001354692.1:c.*65G>A (RAF1) NP_001341621.1:n.*65G>A
NM_001354693.1:c.*65G>A (RAF1) NP_001341622.1:n.*65G>A
NM_001354694.1:c.*65G>A (RAF1) NP_001341623.1:n.*65G>A
NM_001354695.1:c.*65G>A (RAF1) NP_001341624.1:n.*65G>A
NR_148940.1:n.2540G>A (RAF1)
NR_148941.1:n.2486G>A (RAF1)
NR_148942.1:n.2425G>A (RAF1)
XM_011533974.3:c.*65G>A (RAF1) XP_011532276.1:n.*65G>A
XM_017006966.1:c.*65G>A (RAF1) XP_016862455.1:n.*65G>A
NM_001354689.3:c.*65G>A (RAF1) NP_001341618.1:n.*65G>A
NM_001354690.2:c.*65G>A (RAF1) NP_001341619.1:n.*65G>A
NM_001354691.2:c.*65G>A (RAF1) NP_001341620.1:n.*65G>A
NM_001354692.2:c.*65G>A (RAF1) NP_001341621.1:n.*65G>A
NM_001354693.2:c.*65G>A (RAF1) NP_001341622.1:n.*65G>A
NM_001354694.2:c.*65G>A (RAF1) NP_001341623.1:n.*65G>A
NM_001354695.2:c.*65G>A (RAF1) NP_001341624.1:n.*65G>A
NR_148940.2:n.2456G>A (RAF1)
NR_148941.2:n.2402G>A (RAF1)
NR_148942.2:n.2341G>A (RAF1)
NM_001354690.3:c.*65G>A (RAF1) NP_001341619.1:n.*65G>A
NM_001354691.3:c.*65G>A (RAF1) NP_001341620.1:n.*65G>A
NM_001354692.3:c.*65G>A (RAF1) NP_001341621.1:n.*65G>A
NM_001354693.3:c.*65G>A (RAF1) NP_001341622.1:n.*65G>A
NM_001354694.3:c.*65G>A (RAF1) NP_001341623.1:n.*65G>A
NM_001354695.3:c.*65G>A (RAF1) NP_001341624.1:n.*65G>A
NM_002880.4:c.*65G>A (RAF1) MANE Select NP_002871.1:n.*65G>A
NR_148940.3:n.2456G>A (RAF1)
NR_148941.3:n.2402G>A (RAF1)
NR_148942.3:n.2341G>A (RAF1)