Canonical Allele Identifier: CA432272714

Linked Data

dbSNP Id: rs2125317253
MyVariant Identifiers: chr3:g.12626145G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584646G>T , CM000665.2:g.12584646G>T GRCh38
NC_000003.11:g.12626145G>T , CM000665.1:g.12626145G>T GRCh37
NC_000003.10:g.12601145G>T NCBI36
NG_007467.1:g.84534C>A , LRG_413:g.84534C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1480C>A (RAF1) ENSP00000401088.1:n.*1480C>A
ENST00000432427.3:c.1132C>A (RAF1)
ENST00000460610.2:n.6127C>A (RAF1)
ENST00000471449.2:n.625C>A (RAF1)
ENST00000475353.2:n.4095C>A (RAF1)
ENST00000684903.1:c.*1492C>A (RAF1) ENSP00000508612.1:n.*1492C>A
ENST00000685348.1:c.*1526C>A (RAF1) ENSP00000510285.1:n.*1526C>A
ENST00000685437.1:c.1716C>A (RAF1) ENSP00000508794.1:p.Ser572=
ENST00000685653.1:c.1815C>A (RAF1) ENSP00000509968.1:p.Ser605=
ENST00000685697.1:n.2550C>A (RAF1)
ENST00000685738.1:c.*779C>A (RAF1) ENSP00000510156.1:n.*779C>A
ENST00000686409.1:n.5224C>A (RAF1)
ENST00000686455.1:n.4536C>A (RAF1)
ENST00000686762.1:c.*374C>A (RAF1) ENSP00000509767.1:n.*374C>A
ENST00000687257.1:n.4269C>A (RAF1)
ENST00000687326.1:c.*3107C>A (RAF1) ENSP00000509665.1:n.*3107C>A
ENST00000687505.1:n.1933C>A (RAF1)
ENST00000687923.1:c.1704C>A (RAF1) ENSP00000510255.1:p.Ser568=
ENST00000688269.1:n.2411C>A (RAF1)
ENST00000688444.1:n.3932C>A (RAF1)
ENST00000688543.1:c.1716C>A (RAF1) ENSP00000509612.1:p.Ser572=
ENST00000688625.1:c.*3184C>A (RAF1) ENSP00000509522.1:n.*3184C>A
ENST00000688803.1:n.3243C>A (RAF1)
ENST00000689097.1:c.*1492C>A (RAF1) ENSP00000509756.1:n.*1492C>A
ENST00000689389.1:c.1638C>A (RAF1) ENSP00000510213.1:p.Ser546=
ENST00000689418.1:c.*3710C>A (RAF1) ENSP00000509467.1:n.*3710C>A
ENST00000689540.1:n.4183C>A (RAF1)
ENST00000689876.1:c.*364C>A (RAF1) ENSP00000508535.1:n.*364C>A
ENST00000689914.1:c.*749C>A (RAF1) ENSP00000509847.1:n.*749C>A
ENST00000690397.1:c.1704C>A (RAF1) ENSP00000508730.1:p.Ser568=
ENST00000690460.1:c.1803C>A (RAF1) ENSP00000509106.1:p.Ser601=
ENST00000690585.1:c.541C>A (RAF1)
ENST00000690625.1:n.2851C>A (RAF1)
ENST00000691396.1:c.*1687C>A (RAF1) ENSP00000510712.1:n.*1687C>A
ENST00000691643.1:n.2868C>A (RAF1)
ENST00000691724.1:c.*772C>A (RAF1) ENSP00000509255.1:n.*772C>A
ENST00000691779.1:c.*1393C>A (RAF1) ENSP00000508592.1:n.*1393C>A
ENST00000691888.1:c.689C>A (RAF1)
ENST00000691899.1:c.1815C>A (RAF1) ENSP00000508763.1:p.Ser605=
ENST00000692069.1:n.4739C>A (RAF1)
ENST00000692093.1:c.1716C>A (RAF1) ENSP00000509669.1:p.Ser572=
ENST00000692311.1:n.2639C>A (RAF1)
ENST00000692558.1:n.4398C>A (RAF1)
ENST00000692773.1:c.*1552C>A (RAF1) ENSP00000509055.1:n.*1552C>A
ENST00000692830.1:c.*1560C>A (RAF1) ENSP00000509461.1:n.*1560C>A
ENST00000693312.1:c.1590C>A (RAF1) ENSP00000508686.1:p.Ser530=
ENST00000693664.1:c.*266C>A (RAF1) ENSP00000509614.1:n.*266C>A
ENST00000693705.1:c.*1194C>A (RAF1) ENSP00000510697.1:n.*1194C>A
ENST00000251849.9:c.1815C>A (RAF1) MANE Select ENSP00000251849.4:p.Ser605=
ENST00000442415.7:c.1875C>A (RAF1) ENSP00000401888.2:p.Ser625=
ENST00000676541.1:c.*2393G>T (MKRN2) ENSP00000503730.1:n.*2393G>T
ENST00000677142.1:c.*2393G>T (MKRN2) ENSP00000504455.1:n.*2393G>T
ENST00000677816.1:c.*948G>T (MKRN2) ENSP00000502893.1:n.*948G>T
ENST00000677941.1:n.2456G>T (MKRN2)
ENST00000251849.8:c.1815C>A (RAF1) ENSP00000251849.4:p.Ser605=
ENST00000423275.5:c.*1492C>A (RAF1) ENSP00000401088.1:n.*1492C>A
ENST00000432427.2:c.1452C>A (RAF1) ENSP00000398591.2:p.Ser484=
ENST00000442415.6:c.1875C>A (RAF1) ENSP00000401888.2:p.Ser625=
ENST00000471449.1:n.504C>A (RAF1)
NM_002880.3:c.1815C>A , LRG_413t1:c.1815C>A (RAF1) NP_002871.1:p.Ser605=
XM_005265355.1:c.1815C>A (RAF1) XP_005265412.1:p.Ser605=
XM_005265357.1:c.1716C>A (RAF1) XP_005265414.1:p.Ser572=
XM_005265358.3:c.1572C>A (RAF1) XP_005265415.1:p.Ser524=
XM_005265359.3:c.1473C>A (RAF1) XP_005265416.1:p.Ser491=
XM_011533974.1:c.1815C>A (RAF1) XP_011532276.1:p.Ser605=
XM_011533975.1:c.1572C>A (RAF1) XP_011532277.1:p.Ser524=
NM_001354689.1:c.1875C>A (RAF1) NP_001341618.1:p.Ser625=
NM_001354690.1:c.1815C>A (RAF1) NP_001341619.1:p.Ser605=
NM_001354691.1:c.1572C>A (RAF1) NP_001341620.1:p.Ser524=
NM_001354692.1:c.1572C>A (RAF1) NP_001341621.1:p.Ser524=
NM_001354693.1:c.1716C>A (RAF1) NP_001341622.1:p.Ser572=
NM_001354694.1:c.1632C>A (RAF1) NP_001341623.1:p.Ser544=
NM_001354695.1:c.1473C>A (RAF1) NP_001341624.1:p.Ser491=
NR_148940.1:n.2343C>A (RAF1)
NR_148941.1:n.2289C>A (RAF1)
NR_148942.1:n.2228C>A (RAF1)
XM_011533974.3:c.1815C>A (RAF1) XP_011532276.1:p.Ser605=
XM_017006966.1:c.1716C>A (RAF1) XP_016862455.1:p.Ser572=
NM_001354689.3:c.1875C>A (RAF1) NP_001341618.1:p.Ser625=
NM_001354690.2:c.1815C>A (RAF1) NP_001341619.1:p.Ser605=
NM_001354691.2:c.1572C>A (RAF1) NP_001341620.1:p.Ser524=
NM_001354692.2:c.1572C>A (RAF1) NP_001341621.1:p.Ser524=
NM_001354693.2:c.1716C>A (RAF1) NP_001341622.1:p.Ser572=
NM_001354694.2:c.1632C>A (RAF1) NP_001341623.1:p.Ser544=
NM_001354695.2:c.1473C>A (RAF1) NP_001341624.1:p.Ser491=
NR_148940.2:n.2259C>A (RAF1)
NR_148941.2:n.2205C>A (RAF1)
NR_148942.2:n.2144C>A (RAF1)
NM_001354690.3:c.1815C>A (RAF1) NP_001341619.1:p.Ser605=
NM_001354691.3:c.1572C>A (RAF1) NP_001341620.1:p.Ser524=
NM_001354692.3:c.1572C>A (RAF1) NP_001341621.1:p.Ser524=
NM_001354693.3:c.1716C>A (RAF1) NP_001341622.1:p.Ser572=
NM_001354694.3:c.1632C>A (RAF1) NP_001341623.1:p.Ser544=
NM_001354695.3:c.1473C>A (RAF1) NP_001341624.1:p.Ser491=
NM_002880.4:c.1815C>A (RAF1) MANE Select NP_002871.1:p.Ser605=
NR_148940.3:n.2259C>A (RAF1)
NR_148941.3:n.2205C>A (RAF1)
NR_148942.3:n.2144C>A (RAF1)