Canonical Allele Identifier: CA2702189847

Linked Data

dbSNP Id: rs2125317545

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584669C>G , CM000665.2:g.12584669C>G GRCh38
NC_000003.11:g.12626168C>G , CM000665.1:g.12626168C>G GRCh37
NC_000003.10:g.12601168C>G NCBI36
NG_007467.1:g.84511G>C , LRG_413:g.84511G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1469-12G>C (RAF1) ENSP00000401088.1:n.*1469-12G>C
ENST00000432427.3:c.1121-12G>C (RAF1)
ENST00000460610.2:n.6116-12G>C (RAF1)
ENST00000471449.2:n.614-12G>C (RAF1)
ENST00000475353.2:n.4084-12G>C (RAF1)
ENST00000684903.1:c.*1481-12G>C (RAF1) ENSP00000508612.1:n.*1481-12G>C
ENST00000685348.1:c.*1515-12G>C (RAF1) ENSP00000510285.1:n.*1515-12G>C
ENST00000685437.1:c.1705-12G>C (RAF1) ENSP00000508794.1:n.1705-12G>C
ENST00000685653.1:c.1804-12G>C (RAF1) ENSP00000509968.1:n.1804-12G>C
ENST00000685697.1:n.2539-12G>C (RAF1)
ENST00000685738.1:c.*768-12G>C (RAF1) ENSP00000510156.1:n.*768-12G>C
ENST00000686409.1:n.5213-12G>C (RAF1)
ENST00000686455.1:n.4525-12G>C (RAF1)
ENST00000686762.1:c.*363-12G>C (RAF1) ENSP00000509767.1:n.*363-12G>C
ENST00000687257.1:n.4258-12G>C (RAF1)
ENST00000687326.1:c.*3096-12G>C (RAF1) ENSP00000509665.1:n.*3096-12G>C
ENST00000687505.1:n.1922-12G>C (RAF1)
ENST00000687923.1:c.1693-12G>C (RAF1) ENSP00000510255.1:n.1693-12G>C
ENST00000688269.1:n.2400-12G>C (RAF1)
ENST00000688444.1:n.3921-12G>C (RAF1)
ENST00000688543.1:c.1705-12G>C (RAF1) ENSP00000509612.1:n.1705-12G>C
ENST00000688625.1:c.*3173-12G>C (RAF1) ENSP00000509522.1:n.*3173-12G>C
ENST00000688803.1:n.3232-12G>C (RAF1)
ENST00000689097.1:c.*1481-12G>C (RAF1) ENSP00000509756.1:n.*1481-12G>C
ENST00000689389.1:c.1627-12G>C (RAF1) ENSP00000510213.1:n.1627-12G>C
ENST00000689418.1:c.*3699-12G>C (RAF1) ENSP00000509467.1:n.*3699-12G>C
ENST00000689540.1:n.4172-12G>C (RAF1)
ENST00000689876.1:c.*353-12G>C (RAF1) ENSP00000508535.1:n.*353-12G>C
ENST00000689914.1:c.*738-12G>C (RAF1) ENSP00000509847.1:n.*738-12G>C
ENST00000690397.1:c.1693-12G>C (RAF1) ENSP00000508730.1:n.1693-12G>C
ENST00000690460.1:c.1792-12G>C (RAF1) ENSP00000509106.1:n.1792-12G>C
ENST00000690585.1:c.530-12G>C (RAF1)
ENST00000690625.1:n.2840-12G>C (RAF1)
ENST00000691396.1:c.*1676-12G>C (RAF1) ENSP00000510712.1:n.*1676-12G>C
ENST00000691643.1:n.2857-12G>C (RAF1)
ENST00000691724.1:c.*761-12G>C (RAF1) ENSP00000509255.1:n.*761-12G>C
ENST00000691779.1:c.*1382-12G>C (RAF1) ENSP00000508592.1:n.*1382-12G>C
ENST00000691888.1:c.678-12G>C (RAF1)
ENST00000691899.1:c.1804-12G>C (RAF1) ENSP00000508763.1:n.1804-12G>C
ENST00000692069.1:n.4728-12G>C (RAF1)
ENST00000692093.1:c.1705-12G>C (RAF1) ENSP00000509669.1:n.1705-12G>C
ENST00000692311.1:n.2628-12G>C (RAF1)
ENST00000692558.1:n.4387-12G>C (RAF1)
ENST00000692773.1:c.*1541-12G>C (RAF1) ENSP00000509055.1:n.*1541-12G>C
ENST00000692830.1:c.*1549-12G>C (RAF1) ENSP00000509461.1:n.*1549-12G>C
ENST00000693312.1:c.1579-12G>C (RAF1) ENSP00000508686.1:n.1579-12G>C
ENST00000693664.1:c.*255-12G>C (RAF1) ENSP00000509614.1:n.*255-12G>C
ENST00000693705.1:c.*1183-12G>C (RAF1) ENSP00000510697.1:n.*1183-12G>C
ENST00000251849.9:c.1804-12G>C (RAF1) MANE Select ENSP00000251849.4:n.1804-12G>C
ENST00000442415.7:c.1864-12G>C (RAF1) ENSP00000401888.2:n.1864-12G>C
ENST00000676541.1:c.*2416C>G (MKRN2) ENSP00000503730.1:n.*2416C>G
ENST00000677142.1:c.*2416C>G (MKRN2) ENSP00000504455.1:n.*2416C>G
ENST00000677816.1:c.*971C>G (MKRN2) ENSP00000502893.1:n.*971C>G
ENST00000677941.1:n.2479C>G (MKRN2)
ENST00000251849.8:c.1804-12G>C (RAF1) ENSP00000251849.4:n.1804-12G>C
ENST00000423275.5:c.*1481-12G>C (RAF1) ENSP00000401088.1:n.*1481-12G>C
ENST00000432427.2:c.1441-12G>C (RAF1) ENSP00000398591.2:n.1441-12G>C
ENST00000442415.6:c.1864-12G>C (RAF1) ENSP00000401888.2:n.1864-12G>C
ENST00000471449.1:n.493-12G>C (RAF1)
NM_002880.3:c.1804-12G>C , LRG_413t1:c.1804-12G>C (RAF1) NP_002871.1:n.1804-12G>C
XM_005265355.1:c.1804-12G>C (RAF1) XP_005265412.1:n.1804-12G>C
XM_005265357.1:c.1705-12G>C (RAF1) XP_005265414.1:n.1705-12G>C
XM_005265358.3:c.1561-12G>C (RAF1) XP_005265415.1:n.1561-12G>C
XM_005265359.3:c.1462-12G>C (RAF1) XP_005265416.1:n.1462-12G>C
XM_011533974.1:c.1804-12G>C (RAF1) XP_011532276.1:n.1804-12G>C
XM_011533975.1:c.1561-12G>C (RAF1) XP_011532277.1:n.1561-12G>C
NM_001354689.1:c.1864-12G>C (RAF1) NP_001341618.1:n.1864-12G>C
NM_001354690.1:c.1804-12G>C (RAF1) NP_001341619.1:n.1804-12G>C
NM_001354691.1:c.1561-12G>C (RAF1) NP_001341620.1:n.1561-12G>C
NM_001354692.1:c.1561-12G>C (RAF1) NP_001341621.1:n.1561-12G>C
NM_001354693.1:c.1705-12G>C (RAF1) NP_001341622.1:n.1705-12G>C
NM_001354694.1:c.1621-12G>C (RAF1) NP_001341623.1:n.1621-12G>C
NM_001354695.1:c.1462-12G>C (RAF1) NP_001341624.1:n.1462-12G>C
NR_148940.1:n.2332-12G>C (RAF1)
NR_148941.1:n.2278-12G>C (RAF1)
NR_148942.1:n.2217-12G>C (RAF1)
XM_011533974.3:c.1804-12G>C (RAF1) XP_011532276.1:n.1804-12G>C
XM_017006966.1:c.1705-12G>C (RAF1) XP_016862455.1:n.1705-12G>C
NM_001354689.3:c.1864-12G>C (RAF1) NP_001341618.1:n.1864-12G>C
NM_001354690.2:c.1804-12G>C (RAF1) NP_001341619.1:n.1804-12G>C
NM_001354691.2:c.1561-12G>C (RAF1) NP_001341620.1:n.1561-12G>C
NM_001354692.2:c.1561-12G>C (RAF1) NP_001341621.1:n.1561-12G>C
NM_001354693.2:c.1705-12G>C (RAF1) NP_001341622.1:n.1705-12G>C
NM_001354694.2:c.1621-12G>C (RAF1) NP_001341623.1:n.1621-12G>C
NM_001354695.2:c.1462-12G>C (RAF1) NP_001341624.1:n.1462-12G>C
NR_148940.2:n.2248-12G>C (RAF1)
NR_148941.2:n.2194-12G>C (RAF1)
NR_148942.2:n.2133-12G>C (RAF1)
NM_001354690.3:c.1804-12G>C (RAF1) NP_001341619.1:n.1804-12G>C
NM_001354691.3:c.1561-12G>C (RAF1) NP_001341620.1:n.1561-12G>C
NM_001354692.3:c.1561-12G>C (RAF1) NP_001341621.1:n.1561-12G>C
NM_001354693.3:c.1705-12G>C (RAF1) NP_001341622.1:n.1705-12G>C
NM_001354694.3:c.1621-12G>C (RAF1) NP_001341623.1:n.1621-12G>C
NM_001354695.3:c.1462-12G>C (RAF1) NP_001341624.1:n.1462-12G>C
NM_002880.4:c.1804-12G>C (RAF1) MANE Select NP_002871.1:n.1804-12G>C
NR_148940.3:n.2248-12G>C (RAF1)
NR_148941.3:n.2194-12G>C (RAF1)
NR_148942.3:n.2133-12G>C (RAF1)