Canonical Allele Identifier: CA351502457
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590932C>T , CM000665.2:g.12590932C>T GRCh38
NC_000003.11:g.12632431C>T , CM000665.1:g.12632431C>T GRCh37
NC_000003.10:g.12607431C>T NCBI36
NG_007467.1:g.78248G>A , LRG_413:g.78248G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*901G>A ENSP00000401088.1:n.*901G>A
ENST00000432427.3:c.553G>A
ENST00000460610.2:n.30G>A
ENST00000465826.6:n.827G>A
ENST00000475353.2:n.1158G>A
ENST00000494557.2:n.1047G>A
ENST00000684903.1:c.*913G>A ENSP00000508612.1:n.*913G>A
ENST00000685348.1:c.*913G>A ENSP00000510285.1:n.*913G>A
ENST00000685437.1:c.1137G>A ENSP00000508794.1:p.Met379Ile
ENST00000685653.1:c.1236G>A ENSP00000509968.1:p.Met412Ile
ENST00000685738.1:c.*200G>A ENSP00000510156.1:n.*200G>A
ENST00000686409.1:n.2287G>A
ENST00000686455.1:n.1599G>A
ENST00000686762.1:c.1236G>A ENSP00000509767.1:p.Met412Ile
ENST00000687257.1:n.1472G>A
ENST00000687326.1:c.*170G>A ENSP00000509665.1:n.*170G>A
ENST00000687505.1:n.1354G>A
ENST00000687923.1:c.1125G>A ENSP00000510255.1:p.Met375Ile
ENST00000687940.1:n.1613G>A
ENST00000688269.1:n.1832G>A
ENST00000688326.1:c.669G>A
ENST00000688444.1:n.1562G>A
ENST00000688543.1:c.1137G>A ENSP00000509612.1:p.Met379Ile
ENST00000688625.1:c.*814G>A ENSP00000509522.1:n.*814G>A
ENST00000688803.1:n.1467G>A
ENST00000688914.1:n.222G>A
ENST00000689097.1:c.*913G>A ENSP00000509756.1:n.*913G>A
ENST00000689389.1:c.1193+776G>A ENSP00000510213.1:n.1193+776G>A
ENST00000689418.1:c.*913G>A ENSP00000509467.1:n.*913G>A
ENST00000689481.1:c.*913G>A ENSP00000510248.1:n.*913G>A
ENST00000689540.1:n.1386G>A
ENST00000689876.1:c.1236G>A ENSP00000508535.1:p.Met412Ile
ENST00000689914.1:c.*170G>A ENSP00000509847.1:n.*170G>A
ENST00000690397.1:c.1125G>A ENSP00000508730.1:p.Met375Ile
ENST00000690460.1:c.1224G>A ENSP00000509106.1:p.Met408Ile
ENST00000690585.1:c.128G>A
ENST00000690625.1:n.2272G>A
ENST00000691396.1:c.*1088G>A ENSP00000510712.1:n.*1088G>A
ENST00000691724.1:c.*193G>A ENSP00000509255.1:n.*193G>A
ENST00000691779.1:c.*814G>A ENSP00000508592.1:n.*814G>A
ENST00000691888.1:c.128G>A
ENST00000691899.1:c.1236G>A ENSP00000508763.1:p.Met412Ile
ENST00000692069.1:n.1802G>A
ENST00000692093.1:c.1137G>A ENSP00000509669.1:p.Met379Ile
ENST00000692311.1:n.2060G>A
ENST00000692558.1:n.1601G>A
ENST00000692773.1:c.*973G>A ENSP00000509055.1:n.*973G>A
ENST00000692830.1:c.*981G>A ENSP00000509461.1:n.*981G>A
ENST00000693069.1:c.*170G>A ENSP00000510072.1:n.*170G>A
ENST00000693312.1:c.1011G>A ENSP00000508686.1:p.Met337Ile
ENST00000693664.1:c.1236G>A ENSP00000509614.1:p.Met412Ile
ENST00000693705.1:c.*913G>A ENSP00000510697.1:n.*913G>A
ENST00000251849.9:c.1236G>A MANE Select ENSP00000251849.4:p.Met412Ile
ENST00000442415.7:c.1296G>A ENSP00000401888.2:p.Met432Ile
ENST00000251849.8:c.1236G>A ENSP00000251849.4:p.Met412Ile
ENST00000423275.5:c.*913G>A ENSP00000401088.1:n.*913G>A
ENST00000432427.2:c.873G>A ENSP00000398591.2:p.Met291Ile
ENST00000442415.6:c.1296G>A ENSP00000401888.2:p.Met432Ile
ENST00000460610.1:n.193G>A
ENST00000465826.5:n.593G>A
ENST00000475353.1:n.404G>A
ENST00000494557.1:n.252G>A
NM_002880.3:c.1236G>A , LRG_413t1:c.1236G>A NP_002871.1:p.Met412Ile
XM_005265355.1:c.1236G>A XP_005265412.1:p.Met412Ile
XM_005265357.1:c.1137G>A XP_005265414.1:p.Met379Ile
XM_005265358.3:c.993G>A XP_005265415.1:p.Met331Ile
XM_005265359.3:c.894G>A XP_005265416.1:p.Met298Ile
XM_005265360.1:c.1236G>A XP_005265417.1:p.Met412Ile
XM_011533974.1:c.1236G>A XP_011532276.1:p.Met412Ile
XM_011533975.1:c.993G>A XP_011532277.1:p.Met331Ile
NM_001354689.1:c.1296G>A NP_001341618.1:p.Met432Ile
NM_001354690.1:c.1236G>A NP_001341619.1:p.Met412Ile
NM_001354691.1:c.993G>A NP_001341620.1:p.Met331Ile
NM_001354692.1:c.993G>A NP_001341621.1:p.Met331Ile
NM_001354693.1:c.1137G>A NP_001341622.1:p.Met379Ile
NM_001354694.1:c.1053G>A NP_001341623.1:p.Met351Ile
NM_001354695.1:c.894G>A NP_001341624.1:p.Met298Ile
NR_148940.1:n.1764G>A
NR_148941.1:n.1710G>A
NR_148942.1:n.1649G>A
XM_011533974.3:c.1236G>A XP_011532276.1:p.Met412Ile
XM_017006966.1:c.1137G>A XP_016862455.1:p.Met379Ile
NM_001354689.3:c.1296G>A NP_001341618.1:p.Met432Ile
NM_001354690.2:c.1236G>A NP_001341619.1:p.Met412Ile
NM_001354691.2:c.993G>A NP_001341620.1:p.Met331Ile
NM_001354692.2:c.993G>A NP_001341621.1:p.Met331Ile
NM_001354693.2:c.1137G>A NP_001341622.1:p.Met379Ile
NM_001354694.2:c.1053G>A NP_001341623.1:p.Met351Ile
NM_001354695.2:c.894G>A NP_001341624.1:p.Met298Ile
NR_148940.2:n.1680G>A
NR_148941.2:n.1626G>A
NR_148942.2:n.1565G>A
NM_001354690.3:c.1236G>A NP_001341619.1:p.Met412Ile
NM_001354691.3:c.993G>A NP_001341620.1:p.Met331Ile
NM_001354692.3:c.993G>A NP_001341621.1:p.Met331Ile
NM_001354693.3:c.1137G>A NP_001341622.1:p.Met379Ile
NM_001354694.3:c.1053G>A NP_001341623.1:p.Met351Ile
NM_001354695.3:c.894G>A NP_001341624.1:p.Met298Ile
NM_002880.4:c.1236G>A MANE Select NP_002871.1:p.Met412Ile
NR_148940.3:n.1680G>A
NR_148941.3:n.1626G>A
NR_148942.3:n.1565G>A