Canonical Allele Identifier: CA351495500

Linked Data

dbSNP Id: rs1183812590

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1586A>C (RAF1) ENSP00000401088.1:n.*1586A>C
ENST00000432427.3:c.1238A>C (RAF1)
ENST00000460610.2:n.6233A>C (RAF1)
ENST00000471449.2:n.731A>C (RAF1)
ENST00000475353.2:n.4201A>C (RAF1)
ENST00000684903.1:c.*1598A>C (RAF1) ENSP00000508612.1:n.*1598A>C
ENST00000685348.1:c.*1632A>C (RAF1) ENSP00000510285.1:n.*1632A>C
ENST00000685437.1:c.1822A>C (RAF1) ENSP00000508794.1:p.Thr608Pro
ENST00000685653.1:c.1921A>C (RAF1) ENSP00000509968.1:p.Thr641Pro
ENST00000685697.1:n.2656A>C (RAF1)
ENST00000685738.1:c.*885A>C (RAF1) ENSP00000510156.1:n.*885A>C
ENST00000686409.1:n.5330A>C (RAF1)
ENST00000686455.1:n.4642A>C (RAF1)
ENST00000686762.1:c.*480A>C (RAF1) ENSP00000509767.1:n.*480A>C
ENST00000687257.1:n.4375A>C (RAF1)
ENST00000687326.1:c.*3213A>C (RAF1) ENSP00000509665.1:n.*3213A>C
ENST00000687505.1:n.2039A>C (RAF1)
ENST00000687923.1:c.1810A>C (RAF1) ENSP00000510255.1:p.Thr604Pro
ENST00000688269.1:n.2517A>C (RAF1)
ENST00000688444.1:n.4038A>C (RAF1)
ENST00000688543.1:c.1822A>C (RAF1) ENSP00000509612.1:p.Thr608Pro
ENST00000688625.1:c.*3290A>C (RAF1) ENSP00000509522.1:n.*3290A>C
ENST00000688803.1:n.3349A>C (RAF1)
ENST00000689097.1:c.*1598A>C (RAF1) ENSP00000509756.1:n.*1598A>C
ENST00000689389.1:c.1744A>C (RAF1) ENSP00000510213.1:p.Thr582Pro
ENST00000689418.1:c.*3816A>C (RAF1) ENSP00000509467.1:n.*3816A>C
ENST00000689540.1:n.4289A>C (RAF1)
ENST00000689876.1:c.*470A>C (RAF1) ENSP00000508535.1:n.*470A>C
ENST00000689914.1:c.*855A>C (RAF1) ENSP00000509847.1:n.*855A>C
ENST00000690397.1:c.1810A>C (RAF1) ENSP00000508730.1:p.Thr604Pro
ENST00000690460.1:c.1909A>C (RAF1) ENSP00000509106.1:p.Thr637Pro
ENST00000690585.1:c.647A>C (RAF1)
ENST00000690625.1:n.2957A>C (RAF1)
ENST00000691396.1:c.*1793A>C (RAF1) ENSP00000510712.1:n.*1793A>C
ENST00000691643.1:n.2974A>C (RAF1)
ENST00000691724.1:c.*878A>C (RAF1) ENSP00000509255.1:n.*878A>C
ENST00000691779.1:c.*1499A>C (RAF1) ENSP00000508592.1:n.*1499A>C
ENST00000691888.1:c.795A>C (RAF1)
ENST00000691899.1:c.1921A>C (RAF1) ENSP00000508763.1:p.Thr641Pro
ENST00000692069.1:n.4845A>C (RAF1)
ENST00000692093.1:c.1822A>C (RAF1) ENSP00000509669.1:p.Thr608Pro
ENST00000692311.1:n.2745A>C (RAF1)
ENST00000692558.1:n.4504A>C (RAF1)
ENST00000692773.1:c.*1658A>C (RAF1) ENSP00000509055.1:n.*1658A>C
ENST00000692830.1:c.*1666A>C (RAF1) ENSP00000509461.1:n.*1666A>C
ENST00000693312.1:c.1696A>C (RAF1) ENSP00000508686.1:p.Thr566Pro
ENST00000693664.1:c.*372A>C (RAF1) ENSP00000509614.1:n.*372A>C
ENST00000693705.1:c.*1300A>C (RAF1) ENSP00000510697.1:n.*1300A>C
ENST00000251849.9:c.1921A>C (RAF1) MANE Select ENSP00000251849.4:p.Thr641Pro
ENST00000442415.7:c.1981A>C (RAF1) ENSP00000401888.2:p.Thr661Pro
ENST00000676541.1:c.*2287T>G (MKRN2) ENSP00000503730.1:n.*2287T>G
ENST00000677142.1:c.*2287T>G (MKRN2) ENSP00000504455.1:n.*2287T>G
ENST00000677816.1:c.*842T>G (MKRN2) ENSP00000502893.1:n.*842T>G
ENST00000677941.1:n.2350T>G (MKRN2)
ENST00000251849.8:c.1921A>C (RAF1) ENSP00000251849.4:p.Thr641Pro
ENST00000423275.5:c.*1598A>C (RAF1) ENSP00000401088.1:n.*1598A>C
ENST00000432427.2:c.1558A>C (RAF1) ENSP00000398591.2:p.Thr520Pro
ENST00000442415.6:c.1981A>C (RAF1) ENSP00000401888.2:p.Thr661Pro
ENST00000471449.1:n.610A>C (RAF1)
NM_002880.3:c.1921A>C , LRG_413t1:c.1921A>C (RAF1) NP_002871.1:p.Thr641Pro
XM_005265355.1:c.1921A>C (RAF1) XP_005265412.1:p.Thr641Pro
XM_005265357.1:c.1822A>C (RAF1) XP_005265414.1:p.Thr608Pro
XM_005265358.3:c.1678A>C (RAF1) XP_005265415.1:p.Thr560Pro
XM_005265359.3:c.1579A>C (RAF1) XP_005265416.1:p.Thr527Pro
XM_011533974.1:c.1921A>C (RAF1) XP_011532276.1:p.Thr641Pro
XM_011533975.1:c.1678A>C (RAF1) XP_011532277.1:p.Thr560Pro
NM_001354689.1:c.1981A>C (RAF1) NP_001341618.1:p.Thr661Pro
NM_001354690.1:c.1921A>C (RAF1) NP_001341619.1:p.Thr641Pro
NM_001354691.1:c.1678A>C (RAF1) NP_001341620.1:p.Thr560Pro
NM_001354692.1:c.1678A>C (RAF1) NP_001341621.1:p.Thr560Pro
NM_001354693.1:c.1822A>C (RAF1) NP_001341622.1:p.Thr608Pro
NM_001354694.1:c.1738A>C (RAF1) NP_001341623.1:p.Thr580Pro
NM_001354695.1:c.1579A>C (RAF1) NP_001341624.1:p.Thr527Pro
NR_148940.1:n.2449A>C (RAF1)
NR_148941.1:n.2395A>C (RAF1)
NR_148942.1:n.2334A>C (RAF1)
XM_011533974.3:c.1921A>C (RAF1) XP_011532276.1:p.Thr641Pro
XM_017006966.1:c.1822A>C (RAF1) XP_016862455.1:p.Thr608Pro
NM_001354689.3:c.1981A>C (RAF1) NP_001341618.1:p.Thr661Pro
NM_001354690.2:c.1921A>C (RAF1) NP_001341619.1:p.Thr641Pro
NM_001354691.2:c.1678A>C (RAF1) NP_001341620.1:p.Thr560Pro
NM_001354692.2:c.1678A>C (RAF1) NP_001341621.1:p.Thr560Pro
NM_001354693.2:c.1822A>C (RAF1) NP_001341622.1:p.Thr608Pro
NM_001354694.2:c.1738A>C (RAF1) NP_001341623.1:p.Thr580Pro
NM_001354695.2:c.1579A>C (RAF1) NP_001341624.1:p.Thr527Pro
NR_148940.2:n.2365A>C (RAF1)
NR_148941.2:n.2311A>C (RAF1)
NR_148942.2:n.2250A>C (RAF1)
NM_001354690.3:c.1921A>C (RAF1) NP_001341619.1:p.Thr641Pro
NM_001354691.3:c.1678A>C (RAF1) NP_001341620.1:p.Thr560Pro
NM_001354692.3:c.1678A>C (RAF1) NP_001341621.1:p.Thr560Pro
NM_001354693.3:c.1822A>C (RAF1) NP_001341622.1:p.Thr608Pro
NM_001354694.3:c.1738A>C (RAF1) NP_001341623.1:p.Thr580Pro
NM_001354695.3:c.1579A>C (RAF1) NP_001341624.1:p.Thr527Pro
NM_002880.4:c.1921A>C (RAF1) MANE Select NP_002871.1:p.Thr641Pro
NR_148940.3:n.2365A>C (RAF1)
NR_148941.3:n.2311A>C (RAF1)
NR_148942.3:n.2250A>C (RAF1)