Canonical Allele Identifier: CA1346226930

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584972T= , CM000665.2:g.12584972T= GRCh38
NC_000003.11:g.12626471T= , CM000665.1:g.12626471T= GRCh37
NC_000003.10:g.12601471T= NCBI36
NG_007467.1:g.84208A= , LRG_413:g.84208A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1343A= (RAF1) ENSP00000401088.1:n.*1343A=
ENST00000432427.3:c.995A= (RAF1)
ENST00000460610.2:n.5990A= (RAF1)
ENST00000471449.2:n.488A= (RAF1)
ENST00000475353.2:n.3958A= (RAF1)
ENST00000684903.1:c.*1355A= (RAF1) ENSP00000508612.1:n.*1355A=
ENST00000685348.1:c.*1389A= (RAF1) ENSP00000510285.1:n.*1389A=
ENST00000685437.1:c.1579A= (RAF1) ENSP00000508794.1:p.Met527=
ENST00000685653.1:c.1678A= (RAF1) ENSP00000509968.1:p.Met560=
ENST00000685697.1:n.2413A= (RAF1)
ENST00000685738.1:c.*642A= (RAF1) ENSP00000510156.1:n.*642A=
ENST00000686409.1:n.5087A= (RAF1)
ENST00000686455.1:n.4399A= (RAF1)
ENST00000686762.1:c.*237A= (RAF1) ENSP00000509767.1:n.*237A=
ENST00000687257.1:n.4132A= (RAF1)
ENST00000687326.1:c.*2970A= (RAF1) ENSP00000509665.1:n.*2970A=
ENST00000687505.1:n.1796A= (RAF1)
ENST00000687923.1:c.1567A= (RAF1) ENSP00000510255.1:p.Met523=
ENST00000688269.1:n.2274A= (RAF1)
ENST00000688444.1:n.3795A= (RAF1)
ENST00000688543.1:c.1579A= (RAF1) ENSP00000509612.1:p.Met527=
ENST00000688625.1:c.*3047A= (RAF1) ENSP00000509522.1:n.*3047A=
ENST00000688803.1:n.3106A= (RAF1)
ENST00000688914.1:n.1091A= (RAF1)
ENST00000689097.1:c.*1355A= (RAF1) ENSP00000509756.1:n.*1355A=
ENST00000689389.1:c.1501A= (RAF1) ENSP00000510213.1:p.Met501=
ENST00000689418.1:c.*3573A= (RAF1) ENSP00000509467.1:n.*3573A=
ENST00000689540.1:n.4046A= (RAF1)
ENST00000689876.1:c.*227A= (RAF1) ENSP00000508535.1:n.*227A=
ENST00000689914.1:c.*612A= (RAF1) ENSP00000509847.1:n.*612A=
ENST00000690397.1:c.1567A= (RAF1) ENSP00000508730.1:p.Met523=
ENST00000690460.1:c.1666A= (RAF1) ENSP00000509106.1:p.Met556=
ENST00000690585.1:c.404A= (RAF1)
ENST00000690625.1:n.2714A= (RAF1)
ENST00000691396.1:c.*1550A= (RAF1) ENSP00000510712.1:n.*1550A=
ENST00000691643.1:n.2731A= (RAF1)
ENST00000691724.1:c.*635A= (RAF1) ENSP00000509255.1:n.*635A=
ENST00000691779.1:c.*1256A= (RAF1) ENSP00000508592.1:n.*1256A=
ENST00000691888.1:c.552A= (RAF1)
ENST00000691899.1:c.1678A= (RAF1) ENSP00000508763.1:p.Met560=
ENST00000692069.1:n.4602A= (RAF1)
ENST00000692093.1:c.1579A= (RAF1) ENSP00000509669.1:p.Met527=
ENST00000692311.1:n.2502A= (RAF1)
ENST00000692558.1:n.4261A= (RAF1)
ENST00000692773.1:c.*1415A= (RAF1) ENSP00000509055.1:n.*1415A=
ENST00000692830.1:c.*1423A= (RAF1) ENSP00000509461.1:n.*1423A=
ENST00000693312.1:c.1453A= (RAF1) ENSP00000508686.1:p.Met485=
ENST00000693664.1:c.*129A= (RAF1) ENSP00000509614.1:n.*129A=
ENST00000693705.1:c.*1057A= (RAF1) ENSP00000510697.1:n.*1057A=
ENST00000251849.9:c.1678A= (RAF1) MANE Select ENSP00000251849.4:p.Met560=
ENST00000442415.7:c.1738A= (RAF1) ENSP00000401888.2:p.Met580=
ENST00000676541.1:c.*2719T= (MKRN2) ENSP00000503730.1:n.*2719T=
ENST00000677142.1:c.*2719T= (MKRN2) ENSP00000504455.1:n.*2719T=
ENST00000677816.1:c.*1274T= (MKRN2) ENSP00000502893.1:n.*1274T=
ENST00000677941.1:n.2782T= (MKRN2)
ENST00000251849.8:c.1678A= (RAF1) ENSP00000251849.4:p.Met560=
ENST00000423275.5:c.*1355A= (RAF1) ENSP00000401088.1:n.*1355A=
ENST00000432427.2:c.1315A= (RAF1) ENSP00000398591.2:p.Met439=
ENST00000442415.6:c.1738A= (RAF1) ENSP00000401888.2:p.Met580=
ENST00000471449.1:n.367A= (RAF1)
NM_002880.3:c.1678A= , LRG_413t1:c.1678A= (RAF1) NP_002871.1:p.Met560=
XM_005265355.1:c.1678A= (RAF1) XP_005265412.1:p.Met560=
XM_005265357.1:c.1579A= (RAF1) XP_005265414.1:p.Met527=
XM_005265358.3:c.1435A= (RAF1) XP_005265415.1:p.Met479=
XM_005265359.3:c.1336A= (RAF1) XP_005265416.1:p.Met446=
XM_011533974.1:c.1678A= (RAF1) XP_011532276.1:p.Met560=
XM_011533975.1:c.1435A= (RAF1) XP_011532277.1:p.Met479=
NM_001354689.1:c.1738A= (RAF1) NP_001341618.1:p.Met580=
NM_001354690.1:c.1678A= (RAF1) NP_001341619.1:p.Met560=
NM_001354691.1:c.1435A= (RAF1) NP_001341620.1:p.Met479=
NM_001354692.1:c.1435A= (RAF1) NP_001341621.1:p.Met479=
NM_001354693.1:c.1579A= (RAF1) NP_001341622.1:p.Met527=
NM_001354694.1:c.1495A= (RAF1) NP_001341623.1:p.Met499=
NM_001354695.1:c.1336A= (RAF1) NP_001341624.1:p.Met446=
NR_148940.1:n.2206A= (RAF1)
NR_148941.1:n.2152A= (RAF1)
NR_148942.1:n.2091A= (RAF1)
XM_011533974.3:c.1678A= (RAF1) XP_011532276.1:p.Met560=
XM_017006966.1:c.1579A= (RAF1) XP_016862455.1:p.Met527=
NM_001354689.3:c.1738A= (RAF1) NP_001341618.1:p.Met580=
NM_001354690.2:c.1678A= (RAF1) NP_001341619.1:p.Met560=
NM_001354691.2:c.1435A= (RAF1) NP_001341620.1:p.Met479=
NM_001354692.2:c.1435A= (RAF1) NP_001341621.1:p.Met479=
NM_001354693.2:c.1579A= (RAF1) NP_001341622.1:p.Met527=
NM_001354694.2:c.1495A= (RAF1) NP_001341623.1:p.Met499=
NM_001354695.2:c.1336A= (RAF1) NP_001341624.1:p.Met446=
NR_148940.2:n.2122A= (RAF1)
NR_148941.2:n.2068A= (RAF1)
NR_148942.2:n.2007A= (RAF1)
NM_001354690.3:c.1678A= (RAF1) NP_001341619.1:p.Met560=
NM_001354691.3:c.1435A= (RAF1) NP_001341620.1:p.Met479=
NM_001354692.3:c.1435A= (RAF1) NP_001341621.1:p.Met479=
NM_001354693.3:c.1579A= (RAF1) NP_001341622.1:p.Met527=
NM_001354694.3:c.1495A= (RAF1) NP_001341623.1:p.Met499=
NM_001354695.3:c.1336A= (RAF1) NP_001341624.1:p.Met446=
NM_002880.4:c.1678A= (RAF1) MANE Select NP_002871.1:p.Met560=
NR_148940.3:n.2122A= (RAF1)
NR_148941.3:n.2068A= (RAF1)
NR_148942.3:n.2007A= (RAF1)