Canonical Allele Identifier: CA16611127

Linked Data

ClinVar Variation Id: 411093
dbSNP Id: rs1060503152

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584525G>A , CM000665.2:g.12584525G>A GRCh38
NC_000003.11:g.12626024G>A , CM000665.1:g.12626024G>A GRCh37
NC_000003.10:g.12601024G>A NCBI36
NG_007467.1:g.84655C>T , LRG_413:g.84655C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1601C>T (RAF1) ENSP00000401088.1:n.*1601C>T
ENST00000432427.3:c.1253C>T (RAF1)
ENST00000460610.2:n.6248C>T (RAF1)
ENST00000471449.2:n.746C>T (RAF1)
ENST00000475353.2:n.4216C>T (RAF1)
ENST00000684903.1:c.*1613C>T (RAF1) ENSP00000508612.1:n.*1613C>T
ENST00000685348.1:c.*1647C>T (RAF1) ENSP00000510285.1:n.*1647C>T
ENST00000685437.1:c.1837C>T (RAF1) ENSP00000508794.1:p.Pro613Ser
ENST00000685653.1:c.1936C>T (RAF1) ENSP00000509968.1:p.Pro646Ser
ENST00000685697.1:n.2671C>T (RAF1)
ENST00000685738.1:c.*900C>T (RAF1) ENSP00000510156.1:n.*900C>T
ENST00000686409.1:n.5345C>T (RAF1)
ENST00000686455.1:n.4657C>T (RAF1)
ENST00000686762.1:c.*495C>T (RAF1) ENSP00000509767.1:n.*495C>T
ENST00000687257.1:n.4390C>T (RAF1)
ENST00000687326.1:c.*3228C>T (RAF1) ENSP00000509665.1:n.*3228C>T
ENST00000687505.1:n.2054C>T (RAF1)
ENST00000687923.1:c.1825C>T (RAF1) ENSP00000510255.1:p.Pro609Ser
ENST00000688269.1:n.2532C>T (RAF1)
ENST00000688444.1:n.4053C>T (RAF1)
ENST00000688543.1:c.1837C>T (RAF1) ENSP00000509612.1:p.Pro613Ser
ENST00000688625.1:c.*3305C>T (RAF1) ENSP00000509522.1:n.*3305C>T
ENST00000688803.1:n.3364C>T (RAF1)
ENST00000689097.1:c.*1613C>T (RAF1) ENSP00000509756.1:n.*1613C>T
ENST00000689389.1:c.1759C>T (RAF1) ENSP00000510213.1:p.Pro587Ser
ENST00000689418.1:c.*3831C>T (RAF1) ENSP00000509467.1:n.*3831C>T
ENST00000689540.1:n.4304C>T (RAF1)
ENST00000689876.1:c.*485C>T (RAF1) ENSP00000508535.1:n.*485C>T
ENST00000689914.1:c.*870C>T (RAF1) ENSP00000509847.1:n.*870C>T
ENST00000690397.1:c.1825C>T (RAF1) ENSP00000508730.1:p.Pro609Ser
ENST00000690460.1:c.1924C>T (RAF1) ENSP00000509106.1:p.Pro642Ser
ENST00000690585.1:c.662C>T (RAF1)
ENST00000690625.1:n.2972C>T (RAF1)
ENST00000691396.1:c.*1808C>T (RAF1) ENSP00000510712.1:n.*1808C>T
ENST00000691643.1:n.2989C>T (RAF1)
ENST00000691724.1:c.*893C>T (RAF1) ENSP00000509255.1:n.*893C>T
ENST00000691779.1:c.*1514C>T (RAF1) ENSP00000508592.1:n.*1514C>T
ENST00000691888.1:c.810C>T (RAF1)
ENST00000691899.1:c.1936C>T (RAF1) ENSP00000508763.1:p.Pro646Ser
ENST00000692069.1:n.4860C>T (RAF1)
ENST00000692093.1:c.1837C>T (RAF1) ENSP00000509669.1:p.Pro613Ser
ENST00000692311.1:n.2760C>T (RAF1)
ENST00000692558.1:n.4519C>T (RAF1)
ENST00000692773.1:c.*1673C>T (RAF1) ENSP00000509055.1:n.*1673C>T
ENST00000692830.1:c.*1681C>T (RAF1) ENSP00000509461.1:n.*1681C>T
ENST00000693312.1:c.1711C>T (RAF1) ENSP00000508686.1:p.Pro571Ser
ENST00000693664.1:c.*387C>T (RAF1) ENSP00000509614.1:n.*387C>T
ENST00000693705.1:c.*1315C>T (RAF1) ENSP00000510697.1:n.*1315C>T
ENST00000251849.9:c.1936C>T (RAF1) MANE Select ENSP00000251849.4:p.Pro646Ser
ENST00000442415.7:c.1996C>T (RAF1) ENSP00000401888.2:p.Pro666Ser
ENST00000676541.1:c.*2272G>A (MKRN2) ENSP00000503730.1:n.*2272G>A
ENST00000677142.1:c.*2272G>A (MKRN2) ENSP00000504455.1:n.*2272G>A
ENST00000677816.1:c.*827G>A (MKRN2) ENSP00000502893.1:n.*827G>A
ENST00000677941.1:n.2335G>A (MKRN2)
ENST00000251849.8:c.1936C>T (RAF1) ENSP00000251849.4:p.Pro646Ser
ENST00000423275.5:c.*1613C>T (RAF1) ENSP00000401088.1:n.*1613C>T
ENST00000432427.2:c.1573C>T (RAF1) ENSP00000398591.2:p.Pro525Ser
ENST00000442415.6:c.1996C>T (RAF1) ENSP00000401888.2:p.Pro666Ser
ENST00000471449.1:n.625C>T (RAF1)
NM_002880.3:c.1936C>T , LRG_413t1:c.1936C>T (RAF1) NP_002871.1:p.Pro646Ser
XM_005265355.1:c.1936C>T (RAF1) XP_005265412.1:p.Pro646Ser
XM_005265357.1:c.1837C>T (RAF1) XP_005265414.1:p.Pro613Ser
XM_005265358.3:c.1693C>T (RAF1) XP_005265415.1:p.Pro565Ser
XM_005265359.3:c.1594C>T (RAF1) XP_005265416.1:p.Pro532Ser
XM_011533974.1:c.1936C>T (RAF1) XP_011532276.1:p.Pro646Ser
XM_011533975.1:c.1693C>T (RAF1) XP_011532277.1:p.Pro565Ser
NM_001354689.1:c.1996C>T (RAF1) NP_001341618.1:p.Pro666Ser
NM_001354690.1:c.1936C>T (RAF1) NP_001341619.1:p.Pro646Ser
NM_001354691.1:c.1693C>T (RAF1) NP_001341620.1:p.Pro565Ser
NM_001354692.1:c.1693C>T (RAF1) NP_001341621.1:p.Pro565Ser
NM_001354693.1:c.1837C>T (RAF1) NP_001341622.1:p.Pro613Ser
NM_001354694.1:c.1753C>T (RAF1) NP_001341623.1:p.Pro585Ser
NM_001354695.1:c.1594C>T (RAF1) NP_001341624.1:p.Pro532Ser
NR_148940.1:n.2464C>T (RAF1)
NR_148941.1:n.2410C>T (RAF1)
NR_148942.1:n.2349C>T (RAF1)
XM_011533974.3:c.1936C>T (RAF1) XP_011532276.1:p.Pro646Ser
XM_017006966.1:c.1837C>T (RAF1) XP_016862455.1:p.Pro613Ser
NM_001354689.3:c.1996C>T (RAF1) NP_001341618.1:p.Pro666Ser
NM_001354690.2:c.1936C>T (RAF1) NP_001341619.1:p.Pro646Ser
NM_001354691.2:c.1693C>T (RAF1) NP_001341620.1:p.Pro565Ser
NM_001354692.2:c.1693C>T (RAF1) NP_001341621.1:p.Pro565Ser
NM_001354693.2:c.1837C>T (RAF1) NP_001341622.1:p.Pro613Ser
NM_001354694.2:c.1753C>T (RAF1) NP_001341623.1:p.Pro585Ser
NM_001354695.2:c.1594C>T (RAF1) NP_001341624.1:p.Pro532Ser
NR_148940.2:n.2380C>T (RAF1)
NR_148941.2:n.2326C>T (RAF1)
NR_148942.2:n.2265C>T (RAF1)
NM_001354690.3:c.1936C>T (RAF1) NP_001341619.1:p.Pro646Ser
NM_001354691.3:c.1693C>T (RAF1) NP_001341620.1:p.Pro565Ser
NM_001354692.3:c.1693C>T (RAF1) NP_001341621.1:p.Pro565Ser
NM_001354693.3:c.1837C>T (RAF1) NP_001341622.1:p.Pro613Ser
NM_001354694.3:c.1753C>T (RAF1) NP_001341623.1:p.Pro585Ser
NM_001354695.3:c.1594C>T (RAF1) NP_001341624.1:p.Pro532Ser
NM_002880.4:c.1936C>T (RAF1) MANE Select NP_002871.1:p.Pro646Ser
NR_148940.3:n.2380C>T (RAF1)
NR_148941.3:n.2326C>T (RAF1)
NR_148942.3:n.2265C>T (RAF1)