Canonical Allele Identifier: CA351496102

Linked Data

ClinVar Variation Id: 2734444
ClinVar RCV Id: RCV003540147
dbSNP Id: rs1448392469
gnomAD v2: 3-12626126-A-T
gnomAD v3: 3-12584627-A-T
gnomAD v4: 3-12584627-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584627A>T , CM000665.2:g.12584627A>T GRCh38
NC_000003.11:g.12626126A>T , CM000665.1:g.12626126A>T GRCh37
NC_000003.10:g.12601126A>T NCBI36
NG_007467.1:g.84553T>A , LRG_413:g.84553T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1499T>A (RAF1) ENSP00000401088.1:n.*1499T>A
ENST00000432427.3:c.1151T>A (RAF1)
ENST00000460610.2:n.6146T>A (RAF1)
ENST00000471449.2:n.644T>A (RAF1)
ENST00000475353.2:n.4114T>A (RAF1)
ENST00000684903.1:c.*1511T>A (RAF1) ENSP00000508612.1:n.*1511T>A
ENST00000685348.1:c.*1545T>A (RAF1) ENSP00000510285.1:n.*1545T>A
ENST00000685437.1:c.1735T>A (RAF1) ENSP00000508794.1:p.Ser579Thr
ENST00000685653.1:c.1834T>A (RAF1) ENSP00000509968.1:p.Ser612Thr
ENST00000685697.1:n.2569T>A (RAF1)
ENST00000685738.1:c.*798T>A (RAF1) ENSP00000510156.1:n.*798T>A
ENST00000686409.1:n.5243T>A (RAF1)
ENST00000686455.1:n.4555T>A (RAF1)
ENST00000686762.1:c.*393T>A (RAF1) ENSP00000509767.1:n.*393T>A
ENST00000687257.1:n.4288T>A (RAF1)
ENST00000687326.1:c.*3126T>A (RAF1) ENSP00000509665.1:n.*3126T>A
ENST00000687505.1:n.1952T>A (RAF1)
ENST00000687923.1:c.1723T>A (RAF1) ENSP00000510255.1:p.Ser575Thr
ENST00000688269.1:n.2430T>A (RAF1)
ENST00000688444.1:n.3951T>A (RAF1)
ENST00000688543.1:c.1735T>A (RAF1) ENSP00000509612.1:p.Ser579Thr
ENST00000688625.1:c.*3203T>A (RAF1) ENSP00000509522.1:n.*3203T>A
ENST00000688803.1:n.3262T>A (RAF1)
ENST00000689097.1:c.*1511T>A (RAF1) ENSP00000509756.1:n.*1511T>A
ENST00000689389.1:c.1657T>A (RAF1) ENSP00000510213.1:p.Ser553Thr
ENST00000689418.1:c.*3729T>A (RAF1) ENSP00000509467.1:n.*3729T>A
ENST00000689540.1:n.4202T>A (RAF1)
ENST00000689876.1:c.*383T>A (RAF1) ENSP00000508535.1:n.*383T>A
ENST00000689914.1:c.*768T>A (RAF1) ENSP00000509847.1:n.*768T>A
ENST00000690397.1:c.1723T>A (RAF1) ENSP00000508730.1:p.Ser575Thr
ENST00000690460.1:c.1822T>A (RAF1) ENSP00000509106.1:p.Ser608Thr
ENST00000690585.1:c.560T>A (RAF1)
ENST00000690625.1:n.2870T>A (RAF1)
ENST00000691396.1:c.*1706T>A (RAF1) ENSP00000510712.1:n.*1706T>A
ENST00000691643.1:n.2887T>A (RAF1)
ENST00000691724.1:c.*791T>A (RAF1) ENSP00000509255.1:n.*791T>A
ENST00000691779.1:c.*1412T>A (RAF1) ENSP00000508592.1:n.*1412T>A
ENST00000691888.1:c.708T>A (RAF1)
ENST00000691899.1:c.1834T>A (RAF1) ENSP00000508763.1:p.Ser612Thr
ENST00000692069.1:n.4758T>A (RAF1)
ENST00000692093.1:c.1735T>A (RAF1) ENSP00000509669.1:p.Ser579Thr
ENST00000692311.1:n.2658T>A (RAF1)
ENST00000692558.1:n.4417T>A (RAF1)
ENST00000692773.1:c.*1571T>A (RAF1) ENSP00000509055.1:n.*1571T>A
ENST00000692830.1:c.*1579T>A (RAF1) ENSP00000509461.1:n.*1579T>A
ENST00000693312.1:c.1609T>A (RAF1) ENSP00000508686.1:p.Ser537Thr
ENST00000693664.1:c.*285T>A (RAF1) ENSP00000509614.1:n.*285T>A
ENST00000693705.1:c.*1213T>A (RAF1) ENSP00000510697.1:n.*1213T>A
ENST00000251849.9:c.1834T>A (RAF1) MANE Select ENSP00000251849.4:p.Ser612Thr
ENST00000442415.7:c.1894T>A (RAF1) ENSP00000401888.2:p.Ser632Thr
ENST00000676541.1:c.*2374A>T (MKRN2) ENSP00000503730.1:n.*2374A>T
ENST00000677142.1:c.*2374A>T (MKRN2) ENSP00000504455.1:n.*2374A>T
ENST00000677816.1:c.*929A>T (MKRN2) ENSP00000502893.1:n.*929A>T
ENST00000677941.1:n.2437A>T (MKRN2)
ENST00000251849.8:c.1834T>A (RAF1) ENSP00000251849.4:p.Ser612Thr
ENST00000423275.5:c.*1511T>A (RAF1) ENSP00000401088.1:n.*1511T>A
ENST00000432427.2:c.1471T>A (RAF1) ENSP00000398591.2:p.Ser491Thr
ENST00000442415.6:c.1894T>A (RAF1) ENSP00000401888.2:p.Ser632Thr
ENST00000471449.1:n.523T>A (RAF1)
NM_002880.3:c.1834T>A , LRG_413t1:c.1834T>A (RAF1) NP_002871.1:p.Ser612Thr
XM_005265355.1:c.1834T>A (RAF1) XP_005265412.1:p.Ser612Thr
XM_005265357.1:c.1735T>A (RAF1) XP_005265414.1:p.Ser579Thr
XM_005265358.3:c.1591T>A (RAF1) XP_005265415.1:p.Ser531Thr
XM_005265359.3:c.1492T>A (RAF1) XP_005265416.1:p.Ser498Thr
XM_011533974.1:c.1834T>A (RAF1) XP_011532276.1:p.Ser612Thr
XM_011533975.1:c.1591T>A (RAF1) XP_011532277.1:p.Ser531Thr
NM_001354689.1:c.1894T>A (RAF1) NP_001341618.1:p.Ser632Thr
NM_001354690.1:c.1834T>A (RAF1) NP_001341619.1:p.Ser612Thr
NM_001354691.1:c.1591T>A (RAF1) NP_001341620.1:p.Ser531Thr
NM_001354692.1:c.1591T>A (RAF1) NP_001341621.1:p.Ser531Thr
NM_001354693.1:c.1735T>A (RAF1) NP_001341622.1:p.Ser579Thr
NM_001354694.1:c.1651T>A (RAF1) NP_001341623.1:p.Ser551Thr
NM_001354695.1:c.1492T>A (RAF1) NP_001341624.1:p.Ser498Thr
NR_148940.1:n.2362T>A (RAF1)
NR_148941.1:n.2308T>A (RAF1)
NR_148942.1:n.2247T>A (RAF1)
XM_011533974.3:c.1834T>A (RAF1) XP_011532276.1:p.Ser612Thr
XM_017006966.1:c.1735T>A (RAF1) XP_016862455.1:p.Ser579Thr
NM_001354689.3:c.1894T>A (RAF1) NP_001341618.1:p.Ser632Thr
NM_001354690.2:c.1834T>A (RAF1) NP_001341619.1:p.Ser612Thr
NM_001354691.2:c.1591T>A (RAF1) NP_001341620.1:p.Ser531Thr
NM_001354692.2:c.1591T>A (RAF1) NP_001341621.1:p.Ser531Thr
NM_001354693.2:c.1735T>A (RAF1) NP_001341622.1:p.Ser579Thr
NM_001354694.2:c.1651T>A (RAF1) NP_001341623.1:p.Ser551Thr
NM_001354695.2:c.1492T>A (RAF1) NP_001341624.1:p.Ser498Thr
NR_148940.2:n.2278T>A (RAF1)
NR_148941.2:n.2224T>A (RAF1)
NR_148942.2:n.2163T>A (RAF1)
NM_001354690.3:c.1834T>A (RAF1) NP_001341619.1:p.Ser612Thr
NM_001354691.3:c.1591T>A (RAF1) NP_001341620.1:p.Ser531Thr
NM_001354692.3:c.1591T>A (RAF1) NP_001341621.1:p.Ser531Thr
NM_001354693.3:c.1735T>A (RAF1) NP_001341622.1:p.Ser579Thr
NM_001354694.3:c.1651T>A (RAF1) NP_001341623.1:p.Ser551Thr
NM_001354695.3:c.1492T>A (RAF1) NP_001341624.1:p.Ser498Thr
NM_002880.4:c.1834T>A (RAF1) MANE Select NP_002871.1:p.Ser612Thr
NR_148940.3:n.2278T>A (RAF1)
NR_148941.3:n.2224T>A (RAF1)
NR_148942.3:n.2163T>A (RAF1)