Canonical Allele Identifier: CA2701974732

Linked Data

dbSNP Id: rs1559399268

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12585024C>G , CM000665.2:g.12585024C>G GRCh38
NC_000003.11:g.12626523C>G , CM000665.1:g.12626523C>G GRCh37
NC_000003.10:g.12601523C>G NCBI36
NG_007467.1:g.84156G>C , LRG_413:g.84156G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1334-43G>C (RAF1) ENSP00000401088.1:n.*1334-43G>C
ENST00000432427.3:c.986-43G>C (RAF1)
ENST00000460610.2:n.5938G>C (RAF1)
ENST00000471449.2:n.479-43G>C (RAF1)
ENST00000475353.2:n.3906G>C (RAF1)
ENST00000684903.1:c.*1346-43G>C (RAF1) ENSP00000508612.1:n.*1346-43G>C
ENST00000685348.1:c.*1380-43G>C (RAF1) ENSP00000510285.1:n.*1380-43G>C
ENST00000685437.1:c.1570-43G>C (RAF1) ENSP00000508794.1:n.1570-43G>C
ENST00000685653.1:c.1669-43G>C (RAF1) ENSP00000509968.1:n.1669-43G>C
ENST00000685697.1:n.2404-43G>C (RAF1)
ENST00000685738.1:c.*633-43G>C (RAF1) ENSP00000510156.1:n.*633-43G>C
ENST00000686409.1:n.5035G>C (RAF1)
ENST00000686455.1:n.4347G>C (RAF1)
ENST00000686762.1:c.*228-43G>C (RAF1) ENSP00000509767.1:n.*228-43G>C
ENST00000687257.1:n.4123-43G>C (RAF1)
ENST00000687326.1:c.*2918G>C (RAF1) ENSP00000509665.1:n.*2918G>C
ENST00000687505.1:n.1787-43G>C (RAF1)
ENST00000687923.1:c.1558-43G>C (RAF1) ENSP00000510255.1:n.1558-43G>C
ENST00000688269.1:n.2265-43G>C (RAF1)
ENST00000688444.1:n.3786-43G>C (RAF1)
ENST00000688543.1:c.1570-43G>C (RAF1) ENSP00000509612.1:n.1570-43G>C
ENST00000688625.1:c.*3038-43G>C (RAF1) ENSP00000509522.1:n.*3038-43G>C
ENST00000688803.1:n.3097-43G>C (RAF1)
ENST00000688914.1:n.1082-43G>C (RAF1)
ENST00000689097.1:c.*1346-43G>C (RAF1) ENSP00000509756.1:n.*1346-43G>C
ENST00000689389.1:c.1492-43G>C (RAF1) ENSP00000510213.1:n.1492-43G>C
ENST00000689418.1:c.*3564-43G>C (RAF1) ENSP00000509467.1:n.*3564-43G>C
ENST00000689540.1:n.4037-43G>C (RAF1)
ENST00000689876.1:c.*218-43G>C (RAF1) ENSP00000508535.1:n.*218-43G>C
ENST00000689914.1:c.*603-43G>C (RAF1) ENSP00000509847.1:n.*603-43G>C
ENST00000690397.1:c.1558-43G>C (RAF1) ENSP00000508730.1:n.1558-43G>C
ENST00000690460.1:c.1657-43G>C (RAF1) ENSP00000509106.1:n.1657-43G>C
ENST00000690585.1:c.395-43G>C (RAF1)
ENST00000690625.1:n.2705-43G>C (RAF1)
ENST00000691396.1:c.*1541-43G>C (RAF1) ENSP00000510712.1:n.*1541-43G>C
ENST00000691643.1:n.2722-43G>C (RAF1)
ENST00000691724.1:c.*626-43G>C (RAF1) ENSP00000509255.1:n.*626-43G>C
ENST00000691779.1:c.*1247-43G>C (RAF1) ENSP00000508592.1:n.*1247-43G>C
ENST00000691888.1:c.543-43G>C (RAF1)
ENST00000691899.1:c.1669-43G>C (RAF1) ENSP00000508763.1:n.1669-43G>C
ENST00000692069.1:n.4550G>C (RAF1)
ENST00000692093.1:c.1570-43G>C (RAF1) ENSP00000509669.1:n.1570-43G>C
ENST00000692311.1:n.2493-43G>C (RAF1)
ENST00000692558.1:n.4252-43G>C (RAF1)
ENST00000692773.1:c.*1406-43G>C (RAF1) ENSP00000509055.1:n.*1406-43G>C
ENST00000692830.1:c.*1414-43G>C (RAF1) ENSP00000509461.1:n.*1414-43G>C
ENST00000693312.1:c.1444-43G>C (RAF1) ENSP00000508686.1:n.1444-43G>C
ENST00000693664.1:c.*120-43G>C (RAF1) ENSP00000509614.1:n.*120-43G>C
ENST00000693705.1:c.*1048-43G>C (RAF1) ENSP00000510697.1:n.*1048-43G>C
ENST00000251849.9:c.1669-43G>C (RAF1) MANE Select ENSP00000251849.4:n.1669-43G>C
ENST00000442415.7:c.1729-43G>C (RAF1) ENSP00000401888.2:n.1729-43G>C
ENST00000676541.1:c.*2771C>G (MKRN2) ENSP00000503730.1:n.*2771C>G
ENST00000677142.1:c.*2771C>G (MKRN2) ENSP00000504455.1:n.*2771C>G
ENST00000677816.1:c.*1326C>G (MKRN2) ENSP00000502893.1:n.*1326C>G
ENST00000677941.1:n.2834C>G (MKRN2)
ENST00000251849.8:c.1669-43G>C (RAF1) ENSP00000251849.4:n.1669-43G>C
ENST00000423275.5:c.*1346-43G>C (RAF1) ENSP00000401088.1:n.*1346-43G>C
ENST00000432427.2:c.1306-43G>C (RAF1) ENSP00000398591.2:n.1306-43G>C
ENST00000442415.6:c.1729-43G>C (RAF1) ENSP00000401888.2:n.1729-43G>C
ENST00000471449.1:n.358-43G>C (RAF1)
NM_002880.3:c.1669-43G>C , LRG_413t1:c.1669-43G>C (RAF1) NP_002871.1:n.1669-43G>C
XM_005265355.1:c.1669-43G>C (RAF1) XP_005265412.1:n.1669-43G>C
XM_005265357.1:c.1570-43G>C (RAF1) XP_005265414.1:n.1570-43G>C
XM_005265358.3:c.1426-43G>C (RAF1) XP_005265415.1:n.1426-43G>C
XM_005265359.3:c.1327-43G>C (RAF1) XP_005265416.1:n.1327-43G>C
XM_011533974.1:c.1669-43G>C (RAF1) XP_011532276.1:n.1669-43G>C
XM_011533975.1:c.1426-43G>C (RAF1) XP_011532277.1:n.1426-43G>C
NM_001354689.1:c.1729-43G>C (RAF1) NP_001341618.1:n.1729-43G>C
NM_001354690.1:c.1669-43G>C (RAF1) NP_001341619.1:n.1669-43G>C
NM_001354691.1:c.1426-43G>C (RAF1) NP_001341620.1:n.1426-43G>C
NM_001354692.1:c.1426-43G>C (RAF1) NP_001341621.1:n.1426-43G>C
NM_001354693.1:c.1570-43G>C (RAF1) NP_001341622.1:n.1570-43G>C
NM_001354694.1:c.1486-43G>C (RAF1) NP_001341623.1:n.1486-43G>C
NM_001354695.1:c.1327-43G>C (RAF1) NP_001341624.1:n.1327-43G>C
NR_148940.1:n.2197-43G>C (RAF1)
NR_148941.1:n.2143-43G>C (RAF1)
NR_148942.1:n.2082-43G>C (RAF1)
XM_011533974.3:c.1669-43G>C (RAF1) XP_011532276.1:n.1669-43G>C
XM_017006966.1:c.1570-43G>C (RAF1) XP_016862455.1:n.1570-43G>C
NM_001354689.3:c.1729-43G>C (RAF1) NP_001341618.1:n.1729-43G>C
NM_001354690.2:c.1669-43G>C (RAF1) NP_001341619.1:n.1669-43G>C
NM_001354691.2:c.1426-43G>C (RAF1) NP_001341620.1:n.1426-43G>C
NM_001354692.2:c.1426-43G>C (RAF1) NP_001341621.1:n.1426-43G>C
NM_001354693.2:c.1570-43G>C (RAF1) NP_001341622.1:n.1570-43G>C
NM_001354694.2:c.1486-43G>C (RAF1) NP_001341623.1:n.1486-43G>C
NM_001354695.2:c.1327-43G>C (RAF1) NP_001341624.1:n.1327-43G>C
NR_148940.2:n.2113-43G>C (RAF1)
NR_148941.2:n.2059-43G>C (RAF1)
NR_148942.2:n.1998-43G>C (RAF1)
NM_001354690.3:c.1669-43G>C (RAF1) NP_001341619.1:n.1669-43G>C
NM_001354691.3:c.1426-43G>C (RAF1) NP_001341620.1:n.1426-43G>C
NM_001354692.3:c.1426-43G>C (RAF1) NP_001341621.1:n.1426-43G>C
NM_001354693.3:c.1570-43G>C (RAF1) NP_001341622.1:n.1570-43G>C
NM_001354694.3:c.1486-43G>C (RAF1) NP_001341623.1:n.1486-43G>C
NM_001354695.3:c.1327-43G>C (RAF1) NP_001341624.1:n.1327-43G>C
NM_002880.4:c.1669-43G>C (RAF1) MANE Select NP_002871.1:n.1669-43G>C
NR_148940.3:n.2113-43G>C (RAF1)
NR_148941.3:n.2059-43G>C (RAF1)
NR_148942.3:n.1998-43G>C (RAF1)