Canonical Allele Identifier: CA1346233168
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590834A= , CM000665.2:g.12590834A= GRCh38
NC_000003.11:g.12632333A= , CM000665.1:g.12632333A= GRCh37
NC_000003.10:g.12607333A= NCBI36
NG_007467.1:g.78346T= , LRG_413:g.78346T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*999T= ENSP00000401088.1:n.*999T=
ENST00000432427.3:c.651T=
ENST00000460610.2:n.128T=
ENST00000465826.6:n.925T=
ENST00000475353.2:n.1256T=
ENST00000494557.2:n.1145T=
ENST00000684903.1:c.*1011T= ENSP00000508612.1:n.*1011T=
ENST00000685348.1:c.*1011T= ENSP00000510285.1:n.*1011T=
ENST00000685437.1:c.1235T= ENSP00000508794.1:p.Leu412=
ENST00000685653.1:c.1334T= ENSP00000509968.1:p.Leu445=
ENST00000685738.1:c.*298T= ENSP00000510156.1:n.*298T=
ENST00000686409.1:n.2385T=
ENST00000686455.1:n.1697T=
ENST00000686762.1:c.1334T= ENSP00000509767.1:p.Leu445=
ENST00000687257.1:n.1570T=
ENST00000687326.1:c.*268T= ENSP00000509665.1:n.*268T=
ENST00000687505.1:n.1452T=
ENST00000687923.1:c.1223T= ENSP00000510255.1:p.Leu408=
ENST00000687940.1:n.1711T=
ENST00000688269.1:n.1930T=
ENST00000688326.1:c.767T=
ENST00000688444.1:n.1660T=
ENST00000688543.1:c.1235T= ENSP00000509612.1:p.Leu412=
ENST00000688625.1:c.*912T= ENSP00000509522.1:n.*912T=
ENST00000688803.1:n.1565T=
ENST00000688914.1:n.320T=
ENST00000689097.1:c.*1011T= ENSP00000509756.1:n.*1011T=
ENST00000689389.1:c.1193+874T= ENSP00000510213.1:n.1193+874T=
ENST00000689418.1:c.*1011T= ENSP00000509467.1:n.*1011T=
ENST00000689481.1:c.*1011T= ENSP00000510248.1:n.*1011T=
ENST00000689540.1:n.1484T=
ENST00000689876.1:c.1334T= ENSP00000508535.1:p.Leu445=
ENST00000689914.1:c.*268T= ENSP00000509847.1:n.*268T=
ENST00000690397.1:c.1223T= ENSP00000508730.1:p.Leu408=
ENST00000690460.1:c.1322T= ENSP00000509106.1:p.Leu441=
ENST00000690585.1:c.226T=
ENST00000690625.1:n.2370T=
ENST00000691396.1:c.*1186T= ENSP00000510712.1:n.*1186T=
ENST00000691724.1:c.*291T= ENSP00000509255.1:n.*291T=
ENST00000691779.1:c.*912T= ENSP00000508592.1:n.*912T=
ENST00000691888.1:c.226T=
ENST00000691899.1:c.1334T= ENSP00000508763.1:p.Leu445=
ENST00000692069.1:n.1900T=
ENST00000692093.1:c.1235T= ENSP00000509669.1:p.Leu412=
ENST00000692311.1:n.2158T=
ENST00000692558.1:n.1699T=
ENST00000692773.1:c.*1071T= ENSP00000509055.1:n.*1071T=
ENST00000692830.1:c.*1079T= ENSP00000509461.1:n.*1079T=
ENST00000693069.1:c.*268T= ENSP00000510072.1:n.*268T=
ENST00000693312.1:c.1109T= ENSP00000508686.1:p.Leu370=
ENST00000693664.1:c.1334T= ENSP00000509614.1:p.Leu445=
ENST00000693705.1:c.*1011T= ENSP00000510697.1:n.*1011T=
ENST00000251849.9:c.1334T= MANE Select ENSP00000251849.4:p.Leu445=
ENST00000442415.7:c.1394T= ENSP00000401888.2:p.Leu465=
ENST00000251849.8:c.1334T= ENSP00000251849.4:p.Leu445=
ENST00000423275.5:c.*1011T= ENSP00000401088.1:n.*1011T=
ENST00000432427.2:c.971T= ENSP00000398591.2:p.Leu324=
ENST00000442415.6:c.1394T= ENSP00000401888.2:p.Leu465=
ENST00000460610.1:n.291T=
ENST00000465826.5:n.691T=
ENST00000475353.1:n.502T=
ENST00000494557.1:n.350T=
NM_002880.3:c.1334T= , LRG_413t1:c.1334T= NP_002871.1:p.Leu445=
XM_005265355.1:c.1334T= XP_005265412.1:p.Leu445=
XM_005265357.1:c.1235T= XP_005265414.1:p.Leu412=
XM_005265358.3:c.1091T= XP_005265415.1:p.Leu364=
XM_005265359.3:c.992T= XP_005265416.1:p.Leu331=
XM_005265360.1:c.1334T= XP_005265417.1:p.Leu445=
XM_011533974.1:c.1334T= XP_011532276.1:p.Leu445=
XM_011533975.1:c.1091T= XP_011532277.1:p.Leu364=
NM_001354689.1:c.1394T= NP_001341618.1:p.Leu465=
NM_001354690.1:c.1334T= NP_001341619.1:p.Leu445=
NM_001354691.1:c.1091T= NP_001341620.1:p.Leu364=
NM_001354692.1:c.1091T= NP_001341621.1:p.Leu364=
NM_001354693.1:c.1235T= NP_001341622.1:p.Leu412=
NM_001354694.1:c.1151T= NP_001341623.1:p.Leu384=
NM_001354695.1:c.992T= NP_001341624.1:p.Leu331=
NR_148940.1:n.1862T=
NR_148941.1:n.1808T=
NR_148942.1:n.1747T=
XM_011533974.3:c.1334T= XP_011532276.1:p.Leu445=
XM_017006966.1:c.1235T= XP_016862455.1:p.Leu412=
NM_001354689.3:c.1394T= NP_001341618.1:p.Leu465=
NM_001354690.2:c.1334T= NP_001341619.1:p.Leu445=
NM_001354691.2:c.1091T= NP_001341620.1:p.Leu364=
NM_001354692.2:c.1091T= NP_001341621.1:p.Leu364=
NM_001354693.2:c.1235T= NP_001341622.1:p.Leu412=
NM_001354694.2:c.1151T= NP_001341623.1:p.Leu384=
NM_001354695.2:c.992T= NP_001341624.1:p.Leu331=
NR_148940.2:n.1778T=
NR_148941.2:n.1724T=
NR_148942.2:n.1663T=
NM_001354690.3:c.1334T= NP_001341619.1:p.Leu445=
NM_001354691.3:c.1091T= NP_001341620.1:p.Leu364=
NM_001354692.3:c.1091T= NP_001341621.1:p.Leu364=
NM_001354693.3:c.1235T= NP_001341622.1:p.Leu412=
NM_001354694.3:c.1151T= NP_001341623.1:p.Leu384=
NM_001354695.3:c.992T= NP_001341624.1:p.Leu331=
NM_002880.4:c.1334T= MANE Select NP_002871.1:p.Leu445=
NR_148940.3:n.1778T=
NR_148941.3:n.1724T=
NR_148942.3:n.1663T=