Canonical Allele Identifier: CA351501628
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590800C>T , CM000665.2:g.12590800C>T GRCh38
NC_000003.11:g.12632299C>T , CM000665.1:g.12632299C>T GRCh37
NC_000003.10:g.12607299C>T NCBI36
NG_007467.1:g.78380G>A , LRG_413:g.78380G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1033G>A ENSP00000401088.1:n.*1033G>A
ENST00000432427.3:c.685G>A
ENST00000460610.2:n.162G>A
ENST00000465826.6:n.959G>A
ENST00000475353.2:n.1290G>A
ENST00000494557.2:n.1179G>A
ENST00000684903.1:c.*1045G>A ENSP00000508612.1:n.*1045G>A
ENST00000685348.1:c.*1045G>A ENSP00000510285.1:n.*1045G>A
ENST00000685437.1:c.1269G>A ENSP00000508794.1:p.Met423Ile
ENST00000685653.1:c.1368G>A ENSP00000509968.1:p.Met456Ile
ENST00000685738.1:c.*332G>A ENSP00000510156.1:n.*332G>A
ENST00000686409.1:n.2419G>A
ENST00000686455.1:n.1731G>A
ENST00000686762.1:c.1368G>A ENSP00000509767.1:p.Met456Ile
ENST00000687257.1:n.1604G>A
ENST00000687326.1:c.*302G>A ENSP00000509665.1:n.*302G>A
ENST00000687505.1:n.1486G>A
ENST00000687923.1:c.1257G>A ENSP00000510255.1:p.Met419Ile
ENST00000687940.1:n.1745G>A
ENST00000688269.1:n.1964G>A
ENST00000688326.1:c.801G>A
ENST00000688444.1:n.1694G>A
ENST00000688543.1:c.1269G>A ENSP00000509612.1:p.Met423Ile
ENST00000688625.1:c.*946G>A ENSP00000509522.1:n.*946G>A
ENST00000688803.1:n.1599G>A
ENST00000688914.1:n.354G>A
ENST00000689097.1:c.*1045G>A ENSP00000509756.1:n.*1045G>A
ENST00000689389.1:c.1193+908G>A ENSP00000510213.1:n.1193+908G>A
ENST00000689418.1:c.*1045G>A ENSP00000509467.1:n.*1045G>A
ENST00000689481.1:c.*1045G>A ENSP00000510248.1:n.*1045G>A
ENST00000689540.1:n.1518G>A
ENST00000689876.1:c.1368G>A ENSP00000508535.1:p.Met456Ile
ENST00000689914.1:c.*302G>A ENSP00000509847.1:n.*302G>A
ENST00000690397.1:c.1257G>A ENSP00000508730.1:p.Met419Ile
ENST00000690460.1:c.1356G>A ENSP00000509106.1:p.Met452Ile
ENST00000690585.1:c.260G>A
ENST00000690625.1:n.2404G>A
ENST00000691396.1:c.*1220G>A ENSP00000510712.1:n.*1220G>A
ENST00000691724.1:c.*325G>A ENSP00000509255.1:n.*325G>A
ENST00000691779.1:c.*946G>A ENSP00000508592.1:n.*946G>A
ENST00000691888.1:c.260G>A
ENST00000691899.1:c.1368G>A ENSP00000508763.1:p.Met456Ile
ENST00000692069.1:n.1934G>A
ENST00000692093.1:c.1269G>A ENSP00000509669.1:p.Met423Ile
ENST00000692311.1:n.2192G>A
ENST00000692558.1:n.1733G>A
ENST00000692773.1:c.*1105G>A ENSP00000509055.1:n.*1105G>A
ENST00000692830.1:c.*1113G>A ENSP00000509461.1:n.*1113G>A
ENST00000693069.1:c.*302G>A ENSP00000510072.1:n.*302G>A
ENST00000693312.1:c.1143G>A ENSP00000508686.1:p.Met381Ile
ENST00000693664.1:c.1368G>A ENSP00000509614.1:p.Met456Ile
ENST00000693705.1:c.*1045G>A ENSP00000510697.1:n.*1045G>A
ENST00000251849.9:c.1368G>A MANE Select ENSP00000251849.4:p.Met456Ile
ENST00000442415.7:c.1428G>A ENSP00000401888.2:p.Met476Ile
ENST00000251849.8:c.1368G>A ENSP00000251849.4:p.Met456Ile
ENST00000423275.5:c.*1045G>A ENSP00000401088.1:n.*1045G>A
ENST00000432427.2:c.1005G>A ENSP00000398591.2:p.Met335Ile
ENST00000442415.6:c.1428G>A ENSP00000401888.2:p.Met476Ile
ENST00000460610.1:n.325G>A
ENST00000465826.5:n.725G>A
ENST00000475353.1:n.536G>A
ENST00000494557.1:n.384G>A
NM_002880.3:c.1368G>A , LRG_413t1:c.1368G>A NP_002871.1:p.Met456Ile
XM_005265355.1:c.1368G>A XP_005265412.1:p.Met456Ile
XM_005265357.1:c.1269G>A XP_005265414.1:p.Met423Ile
XM_005265358.3:c.1125G>A XP_005265415.1:p.Met375Ile
XM_005265359.3:c.1026G>A XP_005265416.1:p.Met342Ile
XM_005265360.1:c.1368G>A XP_005265417.1:p.Met456Ile
XM_011533974.1:c.1368G>A XP_011532276.1:p.Met456Ile
XM_011533975.1:c.1125G>A XP_011532277.1:p.Met375Ile
NM_001354689.1:c.1428G>A NP_001341618.1:p.Met476Ile
NM_001354690.1:c.1368G>A NP_001341619.1:p.Met456Ile
NM_001354691.1:c.1125G>A NP_001341620.1:p.Met375Ile
NM_001354692.1:c.1125G>A NP_001341621.1:p.Met375Ile
NM_001354693.1:c.1269G>A NP_001341622.1:p.Met423Ile
NM_001354694.1:c.1185G>A NP_001341623.1:p.Met395Ile
NM_001354695.1:c.1026G>A NP_001341624.1:p.Met342Ile
NR_148940.1:n.1896G>A
NR_148941.1:n.1842G>A
NR_148942.1:n.1781G>A
XM_011533974.3:c.1368G>A XP_011532276.1:p.Met456Ile
XM_017006966.1:c.1269G>A XP_016862455.1:p.Met423Ile
NM_001354689.3:c.1428G>A NP_001341618.1:p.Met476Ile
NM_001354690.2:c.1368G>A NP_001341619.1:p.Met456Ile
NM_001354691.2:c.1125G>A NP_001341620.1:p.Met375Ile
NM_001354692.2:c.1125G>A NP_001341621.1:p.Met375Ile
NM_001354693.2:c.1269G>A NP_001341622.1:p.Met423Ile
NM_001354694.2:c.1185G>A NP_001341623.1:p.Met395Ile
NM_001354695.2:c.1026G>A NP_001341624.1:p.Met342Ile
NR_148940.2:n.1812G>A
NR_148941.2:n.1758G>A
NR_148942.2:n.1697G>A
NM_001354690.3:c.1368G>A NP_001341619.1:p.Met456Ile
NM_001354691.3:c.1125G>A NP_001341620.1:p.Met375Ile
NM_001354692.3:c.1125G>A NP_001341621.1:p.Met375Ile
NM_001354693.3:c.1269G>A NP_001341622.1:p.Met423Ile
NM_001354694.3:c.1185G>A NP_001341623.1:p.Met395Ile
NM_001354695.3:c.1026G>A NP_001341624.1:p.Met342Ile
NM_002880.4:c.1368G>A MANE Select NP_002871.1:p.Met456Ile
NR_148940.3:n.1812G>A
NR_148941.3:n.1758G>A
NR_148942.3:n.1697G>A