Canonical Allele Identifier: CA1346226096

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584540T= , CM000665.2:g.12584540T= GRCh38
NC_000003.11:g.12626039T= , CM000665.1:g.12626039T= GRCh37
NC_000003.10:g.12601039T= NCBI36
NG_007467.1:g.84640A= , LRG_413:g.84640A=

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1586A= (RAF1) ENSP00000401088.1:n.*1586A=
ENST00000432427.3:c.1238A= (RAF1)
ENST00000460610.2:n.6233A= (RAF1)
ENST00000471449.2:n.731A= (RAF1)
ENST00000475353.2:n.4201A= (RAF1)
ENST00000684903.1:c.*1598A= (RAF1) ENSP00000508612.1:n.*1598A=
ENST00000685348.1:c.*1632A= (RAF1) ENSP00000510285.1:n.*1632A=
ENST00000685437.1:c.1822A= (RAF1) ENSP00000508794.1:p.Thr608=
ENST00000685653.1:c.1921A= (RAF1) ENSP00000509968.1:p.Thr641=
ENST00000685697.1:n.2656A= (RAF1)
ENST00000685738.1:c.*885A= (RAF1) ENSP00000510156.1:n.*885A=
ENST00000686409.1:n.5330A= (RAF1)
ENST00000686455.1:n.4642A= (RAF1)
ENST00000686762.1:c.*480A= (RAF1) ENSP00000509767.1:n.*480A=
ENST00000687257.1:n.4375A= (RAF1)
ENST00000687326.1:c.*3213A= (RAF1) ENSP00000509665.1:n.*3213A=
ENST00000687505.1:n.2039A= (RAF1)
ENST00000687923.1:c.1810A= (RAF1) ENSP00000510255.1:p.Thr604=
ENST00000688269.1:n.2517A= (RAF1)
ENST00000688444.1:n.4038A= (RAF1)
ENST00000688543.1:c.1822A= (RAF1) ENSP00000509612.1:p.Thr608=
ENST00000688625.1:c.*3290A= (RAF1) ENSP00000509522.1:n.*3290A=
ENST00000688803.1:n.3349A= (RAF1)
ENST00000689097.1:c.*1598A= (RAF1) ENSP00000509756.1:n.*1598A=
ENST00000689389.1:c.1744A= (RAF1) ENSP00000510213.1:p.Thr582=
ENST00000689418.1:c.*3816A= (RAF1) ENSP00000509467.1:n.*3816A=
ENST00000689540.1:n.4289A= (RAF1)
ENST00000689876.1:c.*470A= (RAF1) ENSP00000508535.1:n.*470A=
ENST00000689914.1:c.*855A= (RAF1) ENSP00000509847.1:n.*855A=
ENST00000690397.1:c.1810A= (RAF1) ENSP00000508730.1:p.Thr604=
ENST00000690460.1:c.1909A= (RAF1) ENSP00000509106.1:p.Thr637=
ENST00000690585.1:c.647A= (RAF1)
ENST00000690625.1:n.2957A= (RAF1)
ENST00000691396.1:c.*1793A= (RAF1) ENSP00000510712.1:n.*1793A=
ENST00000691643.1:n.2974A= (RAF1)
ENST00000691724.1:c.*878A= (RAF1) ENSP00000509255.1:n.*878A=
ENST00000691779.1:c.*1499A= (RAF1) ENSP00000508592.1:n.*1499A=
ENST00000691888.1:c.795A= (RAF1)
ENST00000691899.1:c.1921A= (RAF1) ENSP00000508763.1:p.Thr641=
ENST00000692069.1:n.4845A= (RAF1)
ENST00000692093.1:c.1822A= (RAF1) ENSP00000509669.1:p.Thr608=
ENST00000692311.1:n.2745A= (RAF1)
ENST00000692558.1:n.4504A= (RAF1)
ENST00000692773.1:c.*1658A= (RAF1) ENSP00000509055.1:n.*1658A=
ENST00000692830.1:c.*1666A= (RAF1) ENSP00000509461.1:n.*1666A=
ENST00000693312.1:c.1696A= (RAF1) ENSP00000508686.1:p.Thr566=
ENST00000693664.1:c.*372A= (RAF1) ENSP00000509614.1:n.*372A=
ENST00000693705.1:c.*1300A= (RAF1) ENSP00000510697.1:n.*1300A=
ENST00000251849.9:c.1921A= (RAF1) MANE Select ENSP00000251849.4:p.Thr641=
ENST00000442415.7:c.1981A= (RAF1) ENSP00000401888.2:p.Thr661=
ENST00000676541.1:c.*2287T= (MKRN2) ENSP00000503730.1:n.*2287T=
ENST00000677142.1:c.*2287T= (MKRN2) ENSP00000504455.1:n.*2287T=
ENST00000677816.1:c.*842T= (MKRN2) ENSP00000502893.1:n.*842T=
ENST00000677941.1:n.2350T= (MKRN2)
ENST00000251849.8:c.1921A= (RAF1) ENSP00000251849.4:p.Thr641=
ENST00000423275.5:c.*1598A= (RAF1) ENSP00000401088.1:n.*1598A=
ENST00000432427.2:c.1558A= (RAF1) ENSP00000398591.2:p.Thr520=
ENST00000442415.6:c.1981A= (RAF1) ENSP00000401888.2:p.Thr661=
ENST00000471449.1:n.610A= (RAF1)
NM_002880.3:c.1921A= , LRG_413t1:c.1921A= (RAF1) NP_002871.1:p.Thr641=
XM_005265355.1:c.1921A= (RAF1) XP_005265412.1:p.Thr641=
XM_005265357.1:c.1822A= (RAF1) XP_005265414.1:p.Thr608=
XM_005265358.3:c.1678A= (RAF1) XP_005265415.1:p.Thr560=
XM_005265359.3:c.1579A= (RAF1) XP_005265416.1:p.Thr527=
XM_011533974.1:c.1921A= (RAF1) XP_011532276.1:p.Thr641=
XM_011533975.1:c.1678A= (RAF1) XP_011532277.1:p.Thr560=
NM_001354689.1:c.1981A= (RAF1) NP_001341618.1:p.Thr661=
NM_001354690.1:c.1921A= (RAF1) NP_001341619.1:p.Thr641=
NM_001354691.1:c.1678A= (RAF1) NP_001341620.1:p.Thr560=
NM_001354692.1:c.1678A= (RAF1) NP_001341621.1:p.Thr560=
NM_001354693.1:c.1822A= (RAF1) NP_001341622.1:p.Thr608=
NM_001354694.1:c.1738A= (RAF1) NP_001341623.1:p.Thr580=
NM_001354695.1:c.1579A= (RAF1) NP_001341624.1:p.Thr527=
NR_148940.1:n.2449A= (RAF1)
NR_148941.1:n.2395A= (RAF1)
NR_148942.1:n.2334A= (RAF1)
XM_011533974.3:c.1921A= (RAF1) XP_011532276.1:p.Thr641=
XM_017006966.1:c.1822A= (RAF1) XP_016862455.1:p.Thr608=
NM_001354689.3:c.1981A= (RAF1) NP_001341618.1:p.Thr661=
NM_001354690.2:c.1921A= (RAF1) NP_001341619.1:p.Thr641=
NM_001354691.2:c.1678A= (RAF1) NP_001341620.1:p.Thr560=
NM_001354692.2:c.1678A= (RAF1) NP_001341621.1:p.Thr560=
NM_001354693.2:c.1822A= (RAF1) NP_001341622.1:p.Thr608=
NM_001354694.2:c.1738A= (RAF1) NP_001341623.1:p.Thr580=
NM_001354695.2:c.1579A= (RAF1) NP_001341624.1:p.Thr527=
NR_148940.2:n.2365A= (RAF1)
NR_148941.2:n.2311A= (RAF1)
NR_148942.2:n.2250A= (RAF1)
NM_001354690.3:c.1921A= (RAF1) NP_001341619.1:p.Thr641=
NM_001354691.3:c.1678A= (RAF1) NP_001341620.1:p.Thr560=
NM_001354692.3:c.1678A= (RAF1) NP_001341621.1:p.Thr560=
NM_001354693.3:c.1822A= (RAF1) NP_001341622.1:p.Thr608=
NM_001354694.3:c.1738A= (RAF1) NP_001341623.1:p.Thr580=
NM_001354695.3:c.1579A= (RAF1) NP_001341624.1:p.Thr527=
NM_002880.4:c.1921A= (RAF1) MANE Select NP_002871.1:p.Thr641=
NR_148940.3:n.2365A= (RAF1)
NR_148941.3:n.2311A= (RAF1)
NR_148942.3:n.2250A= (RAF1)