Canonical Allele Identifier: CA351496412

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584853A>C , CM000665.2:g.12584853A>C GRCh38
NC_000003.11:g.12626352A>C , CM000665.1:g.12626352A>C GRCh37
NC_000003.10:g.12601352A>C NCBI36
NG_007467.1:g.84327T>G , LRG_413:g.84327T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1462T>G (RAF1) ENSP00000401088.1:n.*1462T>G
ENST00000432427.3:c.1114T>G (RAF1)
ENST00000460610.2:n.6109T>G (RAF1)
ENST00000471449.2:n.607T>G (RAF1)
ENST00000475353.2:n.4077T>G (RAF1)
ENST00000684903.1:c.*1474T>G (RAF1) ENSP00000508612.1:n.*1474T>G
ENST00000685348.1:c.*1508T>G (RAF1) ENSP00000510285.1:n.*1508T>G
ENST00000685437.1:c.1698T>G (RAF1) ENSP00000508794.1:p.Phe566Leu
ENST00000685653.1:c.1797T>G (RAF1) ENSP00000509968.1:p.Phe599Leu
ENST00000685697.1:n.2532T>G (RAF1)
ENST00000685738.1:c.*761T>G (RAF1) ENSP00000510156.1:n.*761T>G
ENST00000686409.1:n.5206T>G (RAF1)
ENST00000686455.1:n.4518T>G (RAF1)
ENST00000686762.1:c.*356T>G (RAF1) ENSP00000509767.1:n.*356T>G
ENST00000687257.1:n.4251T>G (RAF1)
ENST00000687326.1:c.*3089T>G (RAF1) ENSP00000509665.1:n.*3089T>G
ENST00000687505.1:n.1915T>G (RAF1)
ENST00000687923.1:c.1686T>G (RAF1) ENSP00000510255.1:p.Phe562Leu
ENST00000688269.1:n.2393T>G (RAF1)
ENST00000688444.1:n.3914T>G (RAF1)
ENST00000688543.1:c.1698T>G (RAF1) ENSP00000509612.1:p.Phe566Leu
ENST00000688625.1:c.*3166T>G (RAF1) ENSP00000509522.1:n.*3166T>G
ENST00000688803.1:n.3225T>G (RAF1)
ENST00000689097.1:c.*1474T>G (RAF1) ENSP00000509756.1:n.*1474T>G
ENST00000689389.1:c.1620T>G (RAF1) ENSP00000510213.1:p.Phe540Leu
ENST00000689418.1:c.*3692T>G (RAF1) ENSP00000509467.1:n.*3692T>G
ENST00000689540.1:n.4165T>G (RAF1)
ENST00000689876.1:c.*346T>G (RAF1) ENSP00000508535.1:n.*346T>G
ENST00000689914.1:c.*731T>G (RAF1) ENSP00000509847.1:n.*731T>G
ENST00000690397.1:c.1686T>G (RAF1) ENSP00000508730.1:p.Phe562Leu
ENST00000690460.1:c.1785T>G (RAF1) ENSP00000509106.1:p.Phe595Leu
ENST00000690585.1:c.523T>G (RAF1)
ENST00000690625.1:n.2833T>G (RAF1)
ENST00000691396.1:c.*1669T>G (RAF1) ENSP00000510712.1:n.*1669T>G
ENST00000691643.1:n.2850T>G (RAF1)
ENST00000691724.1:c.*754T>G (RAF1) ENSP00000509255.1:n.*754T>G
ENST00000691779.1:c.*1375T>G (RAF1) ENSP00000508592.1:n.*1375T>G
ENST00000691888.1:c.671T>G (RAF1)
ENST00000691899.1:c.1797T>G (RAF1) ENSP00000508763.1:p.Phe599Leu
ENST00000692069.1:n.4721T>G (RAF1)
ENST00000692093.1:c.1698T>G (RAF1) ENSP00000509669.1:p.Phe566Leu
ENST00000692311.1:n.2621T>G (RAF1)
ENST00000692558.1:n.4380T>G (RAF1)
ENST00000692773.1:c.*1534T>G (RAF1) ENSP00000509055.1:n.*1534T>G
ENST00000692830.1:c.*1542T>G (RAF1) ENSP00000509461.1:n.*1542T>G
ENST00000693312.1:c.1572T>G (RAF1) ENSP00000508686.1:p.Phe524Leu
ENST00000693664.1:c.*248T>G (RAF1) ENSP00000509614.1:n.*248T>G
ENST00000693705.1:c.*1176T>G (RAF1) ENSP00000510697.1:n.*1176T>G
ENST00000251849.9:c.1797T>G (RAF1) MANE Select ENSP00000251849.4:p.Phe599Leu
ENST00000442415.7:c.1857T>G (RAF1) ENSP00000401888.2:p.Phe619Leu
ENST00000676541.1:c.*2600A>C (MKRN2) ENSP00000503730.1:n.*2600A>C
ENST00000677142.1:c.*2600A>C (MKRN2) ENSP00000504455.1:n.*2600A>C
ENST00000677816.1:c.*1155A>C (MKRN2) ENSP00000502893.1:n.*1155A>C
ENST00000677941.1:n.2663A>C (MKRN2)
ENST00000251849.8:c.1797T>G (RAF1) ENSP00000251849.4:p.Phe599Leu
ENST00000423275.5:c.*1474T>G (RAF1) ENSP00000401088.1:n.*1474T>G
ENST00000432427.2:c.1434T>G (RAF1) ENSP00000398591.2:p.Phe478Leu
ENST00000442415.6:c.1857T>G (RAF1) ENSP00000401888.2:p.Phe619Leu
ENST00000471449.1:n.486T>G (RAF1)
NM_002880.3:c.1797T>G , LRG_413t1:c.1797T>G (RAF1) NP_002871.1:p.Phe599Leu
XM_005265355.1:c.1797T>G (RAF1) XP_005265412.1:p.Phe599Leu
XM_005265357.1:c.1698T>G (RAF1) XP_005265414.1:p.Phe566Leu
XM_005265358.3:c.1554T>G (RAF1) XP_005265415.1:p.Phe518Leu
XM_005265359.3:c.1455T>G (RAF1) XP_005265416.1:p.Phe485Leu
XM_011533974.1:c.1797T>G (RAF1) XP_011532276.1:p.Phe599Leu
XM_011533975.1:c.1554T>G (RAF1) XP_011532277.1:p.Phe518Leu
NM_001354689.1:c.1857T>G (RAF1) NP_001341618.1:p.Phe619Leu
NM_001354690.1:c.1797T>G (RAF1) NP_001341619.1:p.Phe599Leu
NM_001354691.1:c.1554T>G (RAF1) NP_001341620.1:p.Phe518Leu
NM_001354692.1:c.1554T>G (RAF1) NP_001341621.1:p.Phe518Leu
NM_001354693.1:c.1698T>G (RAF1) NP_001341622.1:p.Phe566Leu
NM_001354694.1:c.1614T>G (RAF1) NP_001341623.1:p.Phe538Leu
NM_001354695.1:c.1455T>G (RAF1) NP_001341624.1:p.Phe485Leu
NR_148940.1:n.2325T>G (RAF1)
NR_148941.1:n.2271T>G (RAF1)
NR_148942.1:n.2210T>G (RAF1)
XM_011533974.3:c.1797T>G (RAF1) XP_011532276.1:p.Phe599Leu
XM_017006966.1:c.1698T>G (RAF1) XP_016862455.1:p.Phe566Leu
NM_001354689.3:c.1857T>G (RAF1) NP_001341618.1:p.Phe619Leu
NM_001354690.2:c.1797T>G (RAF1) NP_001341619.1:p.Phe599Leu
NM_001354691.2:c.1554T>G (RAF1) NP_001341620.1:p.Phe518Leu
NM_001354692.2:c.1554T>G (RAF1) NP_001341621.1:p.Phe518Leu
NM_001354693.2:c.1698T>G (RAF1) NP_001341622.1:p.Phe566Leu
NM_001354694.2:c.1614T>G (RAF1) NP_001341623.1:p.Phe538Leu
NM_001354695.2:c.1455T>G (RAF1) NP_001341624.1:p.Phe485Leu
NR_148940.2:n.2241T>G (RAF1)
NR_148941.2:n.2187T>G (RAF1)
NR_148942.2:n.2126T>G (RAF1)
NM_001354690.3:c.1797T>G (RAF1) NP_001341619.1:p.Phe599Leu
NM_001354691.3:c.1554T>G (RAF1) NP_001341620.1:p.Phe518Leu
NM_001354692.3:c.1554T>G (RAF1) NP_001341621.1:p.Phe518Leu
NM_001354693.3:c.1698T>G (RAF1) NP_001341622.1:p.Phe566Leu
NM_001354694.3:c.1614T>G (RAF1) NP_001341623.1:p.Phe538Leu
NM_001354695.3:c.1455T>G (RAF1) NP_001341624.1:p.Phe485Leu
NM_002880.4:c.1797T>G (RAF1) MANE Select NP_002871.1:p.Phe599Leu
NR_148940.3:n.2241T>G (RAF1)
NR_148941.3:n.2187T>G (RAF1)
NR_148942.3:n.2126T>G (RAF1)