Canonical Allele Identifier: CA351502565

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632445A>T (hg19) ; chr3:g.12590946A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590946A>T , CM000665.2:g.12590946A>T	GRCh38
NC_000003.11:g.12632445A>T , CM000665.1:g.12632445A>T	GRCh37
NC_000003.10:g.12607445A>T	NCBI36
NG_007467.1:g.78234T>A , LRG_413:g.78234T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*887T>A	ENSP00000401088.1:n.*887T>A
ENST00000432427.3:c.539T>A
ENST00000460610.2:n.16T>A
ENST00000465826.6:n.813T>A
ENST00000475353.2:n.1144T>A
ENST00000494557.2:n.1033T>A
ENST00000684903.1:c.*899T>A	ENSP00000508612.1:n.*899T>A
ENST00000685348.1:c.*899T>A	ENSP00000510285.1:n.*899T>A
ENST00000685437.1:c.1123T>A	ENSP00000508794.1:p.Phe375Ile
ENST00000685653.1:c.1222T>A	ENSP00000509968.1:p.Phe408Ile
ENST00000685738.1:c.*186T>A	ENSP00000510156.1:n.*186T>A
ENST00000686409.1:n.2273T>A
ENST00000686455.1:n.1585T>A
ENST00000686762.1:c.1222T>A	ENSP00000509767.1:p.Phe408Ile
ENST00000687257.1:n.1458T>A
ENST00000687326.1:c.*156T>A	ENSP00000509665.1:n.*156T>A
ENST00000687505.1:n.1340T>A
ENST00000687923.1:c.1111T>A	ENSP00000510255.1:p.Phe371Ile
ENST00000687940.1:n.1599T>A
ENST00000688269.1:n.1818T>A
ENST00000688326.1:c.655T>A
ENST00000688444.1:n.1548T>A
ENST00000688543.1:c.1123T>A	ENSP00000509612.1:p.Phe375Ile
ENST00000688625.1:c.*800T>A	ENSP00000509522.1:n.*800T>A
ENST00000688803.1:n.1453T>A
ENST00000688914.1:n.208T>A
ENST00000689097.1:c.*899T>A	ENSP00000509756.1:n.*899T>A
ENST00000689389.1:c.1193+762T>A	ENSP00000510213.1:n.1193+762T>A
ENST00000689418.1:c.*899T>A	ENSP00000509467.1:n.*899T>A
ENST00000689481.1:c.*899T>A	ENSP00000510248.1:n.*899T>A
ENST00000689540.1:n.1372T>A
ENST00000689876.1:c.1222T>A	ENSP00000508535.1:p.Phe408Ile
ENST00000689914.1:c.*156T>A	ENSP00000509847.1:n.*156T>A
ENST00000690397.1:c.1111T>A	ENSP00000508730.1:p.Phe371Ile
ENST00000690460.1:c.1210T>A	ENSP00000509106.1:p.Phe404Ile
ENST00000690585.1:c.114T>A
ENST00000690625.1:n.2258T>A
ENST00000691396.1:c.*1074T>A	ENSP00000510712.1:n.*1074T>A
ENST00000691724.1:c.*179T>A	ENSP00000509255.1:n.*179T>A
ENST00000691779.1:c.*800T>A	ENSP00000508592.1:n.*800T>A
ENST00000691888.1:c.114T>A
ENST00000691899.1:c.1222T>A	ENSP00000508763.1:p.Phe408Ile
ENST00000692069.1:n.1788T>A
ENST00000692093.1:c.1123T>A	ENSP00000509669.1:p.Phe375Ile
ENST00000692311.1:n.2046T>A
ENST00000692558.1:n.1587T>A
ENST00000692773.1:c.*959T>A	ENSP00000509055.1:n.*959T>A
ENST00000692830.1:c.*967T>A	ENSP00000509461.1:n.*967T>A
ENST00000693069.1:c.*156T>A	ENSP00000510072.1:n.*156T>A
ENST00000693312.1:c.997T>A	ENSP00000508686.1:p.Phe333Ile
ENST00000693664.1:c.1222T>A	ENSP00000509614.1:p.Phe408Ile
ENST00000693705.1:c.*899T>A	ENSP00000510697.1:n.*899T>A
ENST00000251849.9:c.1222T>A MANE Select	ENSP00000251849.4:p.Phe408Ile
ENST00000442415.7:c.1282T>A	ENSP00000401888.2:p.Phe428Ile
ENST00000251849.8:c.1222T>A	ENSP00000251849.4:p.Phe408Ile
ENST00000423275.5:c.*899T>A	ENSP00000401088.1:n.*899T>A
ENST00000432427.2:c.859T>A	ENSP00000398591.2:p.Phe287Ile
ENST00000442415.6:c.1282T>A	ENSP00000401888.2:p.Phe428Ile
ENST00000460610.1:n.179T>A
ENST00000465826.5:n.579T>A
ENST00000475353.1:n.390T>A
ENST00000494557.1:n.238T>A
NM_002880.3:c.1222T>A , LRG_413t1:c.1222T>A	NP_002871.1:p.Phe408Ile
XM_005265355.1:c.1222T>A	XP_005265412.1:p.Phe408Ile
XM_005265357.1:c.1123T>A	XP_005265414.1:p.Phe375Ile
XM_005265358.3:c.979T>A	XP_005265415.1:p.Phe327Ile
XM_005265359.3:c.880T>A	XP_005265416.1:p.Phe294Ile
XM_005265360.1:c.1222T>A	XP_005265417.1:p.Phe408Ile
XM_011533974.1:c.1222T>A	XP_011532276.1:p.Phe408Ile
XM_011533975.1:c.979T>A	XP_011532277.1:p.Phe327Ile
NM_001354689.1:c.1282T>A	NP_001341618.1:p.Phe428Ile
NM_001354690.1:c.1222T>A	NP_001341619.1:p.Phe408Ile
NM_001354691.1:c.979T>A	NP_001341620.1:p.Phe327Ile
NM_001354692.1:c.979T>A	NP_001341621.1:p.Phe327Ile
NM_001354693.1:c.1123T>A	NP_001341622.1:p.Phe375Ile
NM_001354694.1:c.1039T>A	NP_001341623.1:p.Phe347Ile
NM_001354695.1:c.880T>A	NP_001341624.1:p.Phe294Ile
NR_148940.1:n.1750T>A
NR_148941.1:n.1696T>A
NR_148942.1:n.1635T>A
XM_011533974.3:c.1222T>A	XP_011532276.1:p.Phe408Ile
XM_017006966.1:c.1123T>A	XP_016862455.1:p.Phe375Ile
XR_001740227.1:n.1513T>A
NM_001354689.3:c.1282T>A	NP_001341618.1:p.Phe428Ile
NM_001354690.2:c.1222T>A	NP_001341619.1:p.Phe408Ile
NM_001354691.2:c.979T>A	NP_001341620.1:p.Phe327Ile
NM_001354692.2:c.979T>A	NP_001341621.1:p.Phe327Ile
NM_001354693.2:c.1123T>A	NP_001341622.1:p.Phe375Ile
NM_001354694.2:c.1039T>A	NP_001341623.1:p.Phe347Ile
NM_001354695.2:c.880T>A	NP_001341624.1:p.Phe294Ile
NR_148940.2:n.1666T>A
NR_148941.2:n.1612T>A
NR_148942.2:n.1551T>A
NM_001354690.3:c.1222T>A	NP_001341619.1:p.Phe408Ile
NM_001354691.3:c.979T>A	NP_001341620.1:p.Phe327Ile
NM_001354692.3:c.979T>A	NP_001341621.1:p.Phe327Ile
NM_001354693.3:c.1123T>A	NP_001341622.1:p.Phe375Ile
NM_001354694.3:c.1039T>A	NP_001341623.1:p.Phe347Ile
NM_001354695.3:c.880T>A	NP_001341624.1:p.Phe294Ile
NM_002880.4:c.1222T>A MANE Select	NP_002871.1:p.Phe408Ile
NR_148940.3:n.1666T>A
NR_148941.3:n.1612T>A
NR_148942.3:n.1551T>A