Canonical Allele Identifier: CA1346242599
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600208C= , CM000665.2:g.12600208C= GRCh38
NC_000003.11:g.12641707C= , CM000665.1:g.12641707C= GRCh37
NC_000003.10:g.12616707C= NCBI36
NG_007467.1:g.68972G= , LRG_413:g.68972G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*599G= ENSP00000401088.1:n.*599G=
ENST00000432427.3:c.254G=
ENST00000465826.6:n.525G=
ENST00000491290.2:n.1311G=
ENST00000684903.1:c.*611G= ENSP00000508612.1:n.*611G=
ENST00000685348.1:c.*611G= ENSP00000510285.1:n.*611G=
ENST00000685437.1:c.835G= ENSP00000508794.1:p.Val279=
ENST00000685438.1:n.698G=
ENST00000685653.1:c.934G= ENSP00000509968.1:p.Val312=
ENST00000685738.1:c.934G= ENSP00000510156.1:p.Val312=
ENST00000686409.1:n.1642G=
ENST00000686455.1:n.1297G=
ENST00000686479.1:n.1305G=
ENST00000686762.1:c.934G= ENSP00000509767.1:p.Val312=
ENST00000687257.1:n.1170G=
ENST00000687326.1:c.934G= ENSP00000509665.1:p.Val312=
ENST00000687486.1:c.182+180G=
ENST00000687505.1:n.1052G=
ENST00000687923.1:c.835G= ENSP00000510255.1:p.Val279=
ENST00000687940.1:n.1311G=
ENST00000688269.1:n.1530G=
ENST00000688326.1:c.254G=
ENST00000688444.1:n.1260G=
ENST00000688543.1:c.835G= ENSP00000509612.1:p.Val279=
ENST00000688625.1:c.*512G= ENSP00000509522.1:n.*512G=
ENST00000688803.1:n.1165G=
ENST00000689097.1:c.*611G= ENSP00000509756.1:n.*611G=
ENST00000689389.1:c.934G= ENSP00000510213.1:p.Val312=
ENST00000689418.1:c.*611G= ENSP00000509467.1:n.*611G=
ENST00000689481.1:c.*611G= ENSP00000510248.1:n.*611G=
ENST00000689540.1:n.1084G=
ENST00000689876.1:c.934G= ENSP00000508535.1:p.Val312=
ENST00000689914.1:c.934G= ENSP00000509847.1:p.Val312=
ENST00000690397.1:c.823G= ENSP00000508730.1:p.Val275=
ENST00000690460.1:c.922G= ENSP00000509106.1:p.Val308=
ENST00000690625.1:n.1237G=
ENST00000691268.1:c.361G=
ENST00000691396.1:c.*727G= ENSP00000510712.1:n.*727G=
ENST00000691724.1:c.934G= ENSP00000509255.1:p.Val312=
ENST00000691779.1:c.*512G= ENSP00000508592.1:n.*512G=
ENST00000691899.1:c.934G= ENSP00000508763.1:p.Val312=
ENST00000692069.1:n.1157G=
ENST00000692093.1:c.835G= ENSP00000509669.1:p.Val279=
ENST00000692311.1:n.1415G=
ENST00000692558.1:n.1299G=
ENST00000692773.1:c.*671G= ENSP00000509055.1:n.*671G=
ENST00000692830.1:c.*679G= ENSP00000509461.1:n.*679G=
ENST00000693069.1:c.835G= ENSP00000510072.1:p.Val279=
ENST00000693312.1:c.709G= ENSP00000508686.1:p.Val237=
ENST00000693664.1:c.934G= ENSP00000509614.1:p.Val312=
ENST00000693705.1:c.*611G= ENSP00000510697.1:n.*611G=
ENST00000251849.9:c.934G= MANE Select ENSP00000251849.4:p.Val312=
ENST00000442415.7:c.994G= ENSP00000401888.2:p.Val332=
ENST00000251849.8:c.934G= ENSP00000251849.4:p.Val312=
ENST00000423275.5:c.*611G= ENSP00000401088.1:n.*611G=
ENST00000432427.2:c.571G= ENSP00000398591.2:p.Val191=
ENST00000442415.6:c.994G= ENSP00000401888.2:p.Val332=
ENST00000465826.5:n.178G=
ENST00000491290.1:n.563G=
NM_002880.3:c.934G= , LRG_413t1:c.934G= NP_002871.1:p.Val312=
XM_005265355.1:c.934G= XP_005265412.1:p.Val312=
XM_005265357.1:c.835G= XP_005265414.1:p.Val279=
XM_005265358.3:c.691G= XP_005265415.1:p.Val231=
XM_005265359.3:c.592G= XP_005265416.1:p.Val198=
XM_005265360.1:c.934G= XP_005265417.1:p.Val312=
XM_011533974.1:c.934G= XP_011532276.1:p.Val312=
XM_011533975.1:c.691G= XP_011532277.1:p.Val231=
NM_001354689.1:c.994G= NP_001341618.1:p.Val332=
NM_001354690.1:c.934G= NP_001341619.1:p.Val312=
NM_001354691.1:c.691G= NP_001341620.1:p.Val231=
NM_001354692.1:c.691G= NP_001341621.1:p.Val231=
NM_001354693.1:c.835G= NP_001341622.1:p.Val279=
NM_001354694.1:c.751G= NP_001341623.1:p.Val251=
NM_001354695.1:c.592G= NP_001341624.1:p.Val198=
NR_148940.1:n.1349G=
NR_148941.1:n.1349G=
NR_148942.1:n.1349G=
XM_011533974.3:c.934G= XP_011532276.1:p.Val312=
XM_017006966.1:c.835G= XP_016862455.1:p.Val279=
XR_001740227.1:n.1166G=
NM_001354689.3:c.994G= NP_001341618.1:p.Val332=
NM_001354690.2:c.934G= NP_001341619.1:p.Val312=
NM_001354691.2:c.691G= NP_001341620.1:p.Val231=
NM_001354692.2:c.691G= NP_001341621.1:p.Val231=
NM_001354693.2:c.835G= NP_001341622.1:p.Val279=
NM_001354694.2:c.751G= NP_001341623.1:p.Val251=
NM_001354695.2:c.592G= NP_001341624.1:p.Val198=
NR_148940.2:n.1265G=
NR_148941.2:n.1265G=
NR_148942.2:n.1265G=
NM_001354690.3:c.934G= NP_001341619.1:p.Val312=
NM_001354691.3:c.691G= NP_001341620.1:p.Val231=
NM_001354692.3:c.691G= NP_001341621.1:p.Val231=
NM_001354693.3:c.835G= NP_001341622.1:p.Val279=
NM_001354694.3:c.751G= NP_001341623.1:p.Val251=
NM_001354695.3:c.592G= NP_001341624.1:p.Val198=
NM_002880.4:c.934G= MANE Select NP_002871.1:p.Val312=
NR_148940.3:n.1265G=
NR_148941.3:n.1265G=
NR_148942.3:n.1265G=