Canonical Allele Identifier: CA351496401

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584851G>A , CM000665.2:g.12584851G>A GRCh38
NC_000003.11:g.12626350G>A , CM000665.1:g.12626350G>A GRCh37
NC_000003.10:g.12601350G>A NCBI36
NG_007467.1:g.84329C>T , LRG_413:g.84329C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1464C>T (RAF1) ENSP00000401088.1:n.*1464C>T
ENST00000432427.3:c.1116C>T (RAF1)
ENST00000460610.2:n.6111C>T (RAF1)
ENST00000471449.2:n.609C>T (RAF1)
ENST00000475353.2:n.4079C>T (RAF1)
ENST00000684903.1:c.*1476C>T (RAF1) ENSP00000508612.1:n.*1476C>T
ENST00000685348.1:c.*1510C>T (RAF1) ENSP00000510285.1:n.*1510C>T
ENST00000685437.1:c.1700C>T (RAF1) ENSP00000508794.1:p.Pro567Leu
ENST00000685653.1:c.1799C>T (RAF1) ENSP00000509968.1:p.Pro600Leu
ENST00000685697.1:n.2534C>T (RAF1)
ENST00000685738.1:c.*763C>T (RAF1) ENSP00000510156.1:n.*763C>T
ENST00000686409.1:n.5208C>T (RAF1)
ENST00000686455.1:n.4520C>T (RAF1)
ENST00000686762.1:c.*358C>T (RAF1) ENSP00000509767.1:n.*358C>T
ENST00000687257.1:n.4253C>T (RAF1)
ENST00000687326.1:c.*3091C>T (RAF1) ENSP00000509665.1:n.*3091C>T
ENST00000687505.1:n.1917C>T (RAF1)
ENST00000687923.1:c.1688C>T (RAF1) ENSP00000510255.1:p.Pro563Leu
ENST00000688269.1:n.2395C>T (RAF1)
ENST00000688444.1:n.3916C>T (RAF1)
ENST00000688543.1:c.1700C>T (RAF1) ENSP00000509612.1:p.Pro567Leu
ENST00000688625.1:c.*3168C>T (RAF1) ENSP00000509522.1:n.*3168C>T
ENST00000688803.1:n.3227C>T (RAF1)
ENST00000689097.1:c.*1476C>T (RAF1) ENSP00000509756.1:n.*1476C>T
ENST00000689389.1:c.1622C>T (RAF1) ENSP00000510213.1:p.Pro541Leu
ENST00000689418.1:c.*3694C>T (RAF1) ENSP00000509467.1:n.*3694C>T
ENST00000689540.1:n.4167C>T (RAF1)
ENST00000689876.1:c.*348C>T (RAF1) ENSP00000508535.1:n.*348C>T
ENST00000689914.1:c.*733C>T (RAF1) ENSP00000509847.1:n.*733C>T
ENST00000690397.1:c.1688C>T (RAF1) ENSP00000508730.1:p.Pro563Leu
ENST00000690460.1:c.1787C>T (RAF1) ENSP00000509106.1:p.Pro596Leu
ENST00000690585.1:c.525C>T (RAF1)
ENST00000690625.1:n.2835C>T (RAF1)
ENST00000691396.1:c.*1671C>T (RAF1) ENSP00000510712.1:n.*1671C>T
ENST00000691643.1:n.2852C>T (RAF1)
ENST00000691724.1:c.*756C>T (RAF1) ENSP00000509255.1:n.*756C>T
ENST00000691779.1:c.*1377C>T (RAF1) ENSP00000508592.1:n.*1377C>T
ENST00000691888.1:c.673C>T (RAF1)
ENST00000691899.1:c.1799C>T (RAF1) ENSP00000508763.1:p.Pro600Leu
ENST00000692069.1:n.4723C>T (RAF1)
ENST00000692093.1:c.1700C>T (RAF1) ENSP00000509669.1:p.Pro567Leu
ENST00000692311.1:n.2623C>T (RAF1)
ENST00000692558.1:n.4382C>T (RAF1)
ENST00000692773.1:c.*1536C>T (RAF1) ENSP00000509055.1:n.*1536C>T
ENST00000692830.1:c.*1544C>T (RAF1) ENSP00000509461.1:n.*1544C>T
ENST00000693312.1:c.1574C>T (RAF1) ENSP00000508686.1:p.Pro525Leu
ENST00000693664.1:c.*250C>T (RAF1) ENSP00000509614.1:n.*250C>T
ENST00000693705.1:c.*1178C>T (RAF1) ENSP00000510697.1:n.*1178C>T
ENST00000251849.9:c.1799C>T (RAF1) MANE Select ENSP00000251849.4:p.Pro600Leu
ENST00000442415.7:c.1859C>T (RAF1) ENSP00000401888.2:p.Pro620Leu
ENST00000676541.1:c.*2598G>A (MKRN2) ENSP00000503730.1:n.*2598G>A
ENST00000677142.1:c.*2598G>A (MKRN2) ENSP00000504455.1:n.*2598G>A
ENST00000677816.1:c.*1153G>A (MKRN2) ENSP00000502893.1:n.*1153G>A
ENST00000677941.1:n.2661G>A (MKRN2)
ENST00000251849.8:c.1799C>T (RAF1) ENSP00000251849.4:p.Pro600Leu
ENST00000423275.5:c.*1476C>T (RAF1) ENSP00000401088.1:n.*1476C>T
ENST00000432427.2:c.1436C>T (RAF1) ENSP00000398591.2:p.Pro479Leu
ENST00000442415.6:c.1859C>T (RAF1) ENSP00000401888.2:p.Pro620Leu
ENST00000471449.1:n.488C>T (RAF1)
NM_002880.3:c.1799C>T , LRG_413t1:c.1799C>T (RAF1) NP_002871.1:p.Pro600Leu
XM_005265355.1:c.1799C>T (RAF1) XP_005265412.1:p.Pro600Leu
XM_005265357.1:c.1700C>T (RAF1) XP_005265414.1:p.Pro567Leu
XM_005265358.3:c.1556C>T (RAF1) XP_005265415.1:p.Pro519Leu
XM_005265359.3:c.1457C>T (RAF1) XP_005265416.1:p.Pro486Leu
XM_011533974.1:c.1799C>T (RAF1) XP_011532276.1:p.Pro600Leu
XM_011533975.1:c.1556C>T (RAF1) XP_011532277.1:p.Pro519Leu
NM_001354689.1:c.1859C>T (RAF1) NP_001341618.1:p.Pro620Leu
NM_001354690.1:c.1799C>T (RAF1) NP_001341619.1:p.Pro600Leu
NM_001354691.1:c.1556C>T (RAF1) NP_001341620.1:p.Pro519Leu
NM_001354692.1:c.1556C>T (RAF1) NP_001341621.1:p.Pro519Leu
NM_001354693.1:c.1700C>T (RAF1) NP_001341622.1:p.Pro567Leu
NM_001354694.1:c.1616C>T (RAF1) NP_001341623.1:p.Pro539Leu
NM_001354695.1:c.1457C>T (RAF1) NP_001341624.1:p.Pro486Leu
NR_148940.1:n.2327C>T (RAF1)
NR_148941.1:n.2273C>T (RAF1)
NR_148942.1:n.2212C>T (RAF1)
XM_011533974.3:c.1799C>T (RAF1) XP_011532276.1:p.Pro600Leu
XM_017006966.1:c.1700C>T (RAF1) XP_016862455.1:p.Pro567Leu
NM_001354689.3:c.1859C>T (RAF1) NP_001341618.1:p.Pro620Leu
NM_001354690.2:c.1799C>T (RAF1) NP_001341619.1:p.Pro600Leu
NM_001354691.2:c.1556C>T (RAF1) NP_001341620.1:p.Pro519Leu
NM_001354692.2:c.1556C>T (RAF1) NP_001341621.1:p.Pro519Leu
NM_001354693.2:c.1700C>T (RAF1) NP_001341622.1:p.Pro567Leu
NM_001354694.2:c.1616C>T (RAF1) NP_001341623.1:p.Pro539Leu
NM_001354695.2:c.1457C>T (RAF1) NP_001341624.1:p.Pro486Leu
NR_148940.2:n.2243C>T (RAF1)
NR_148941.2:n.2189C>T (RAF1)
NR_148942.2:n.2128C>T (RAF1)
NM_001354690.3:c.1799C>T (RAF1) NP_001341619.1:p.Pro600Leu
NM_001354691.3:c.1556C>T (RAF1) NP_001341620.1:p.Pro519Leu
NM_001354692.3:c.1556C>T (RAF1) NP_001341621.1:p.Pro519Leu
NM_001354693.3:c.1700C>T (RAF1) NP_001341622.1:p.Pro567Leu
NM_001354694.3:c.1616C>T (RAF1) NP_001341623.1:p.Pro539Leu
NM_001354695.3:c.1457C>T (RAF1) NP_001341624.1:p.Pro486Leu
NM_002880.4:c.1799C>T (RAF1) MANE Select NP_002871.1:p.Pro600Leu
NR_148940.3:n.2243C>T (RAF1)
NR_148941.3:n.2189C>T (RAF1)
NR_148942.3:n.2128C>T (RAF1)