Canonical Allele Identifier: CA432273752

Gene: RAF1

Linked Data

• dbSNP Id: rs2125377613
• MyVariant Identifiers: chr3:g.12641224G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12599725G>A , CM000665.2:g.12599725G>A	GRCh38
NC_000003.11:g.12641224G>A , CM000665.1:g.12641224G>A	GRCh37
NC_000003.10:g.12616224G>A	NCBI36
NG_007467.1:g.69455C>T , LRG_413:g.69455C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*739C>T	ENSP00000401088.1:n.*739C>T
ENST00000432427.3:c.394C>T
ENST00000465826.6:n.665C>T
ENST00000491290.2:n.1451C>T
ENST00000684903.1:c.*751C>T	ENSP00000508612.1:n.*751C>T
ENST00000685348.1:c.*751C>T	ENSP00000510285.1:n.*751C>T
ENST00000685437.1:c.975C>T	ENSP00000508794.1:p.Gly325=
ENST00000685653.1:c.1074C>T	ENSP00000509968.1:p.Gly358=
ENST00000685738.1:c.1074C>T	ENSP00000510156.1:p.Gly358=
ENST00000686409.1:n.2125C>T
ENST00000686455.1:n.1437C>T
ENST00000686479.1:n.1445C>T
ENST00000686762.1:c.1074C>T	ENSP00000509767.1:p.Gly358=
ENST00000687257.1:n.1310C>T
ENST00000687326.1:c.1074C>T	ENSP00000509665.1:p.Gly358=
ENST00000687486.1:c.266C>T
ENST00000687505.1:n.1192C>T
ENST00000687923.1:c.975C>T	ENSP00000510255.1:p.Gly325=
ENST00000687940.1:n.1451C>T
ENST00000688269.1:n.1670C>T
ENST00000688326.1:c.394C>T
ENST00000688444.1:n.1400C>T
ENST00000688543.1:c.975C>T	ENSP00000509612.1:p.Gly325=
ENST00000688625.1:c.*652C>T	ENSP00000509522.1:n.*652C>T
ENST00000688803.1:n.1305C>T
ENST00000688914.1:n.60C>T
ENST00000689097.1:c.*751C>T	ENSP00000509756.1:n.*751C>T
ENST00000689389.1:c.1074C>T	ENSP00000510213.1:p.Gly358=
ENST00000689418.1:c.*751C>T	ENSP00000509467.1:n.*751C>T
ENST00000689481.1:c.*751C>T	ENSP00000510248.1:n.*751C>T
ENST00000689540.1:n.1224C>T
ENST00000689876.1:c.1074C>T	ENSP00000508535.1:p.Gly358=
ENST00000689914.1:c.1074C>T	ENSP00000509847.1:p.Gly358=
ENST00000690397.1:c.963C>T	ENSP00000508730.1:p.Gly321=
ENST00000690460.1:c.1062C>T	ENSP00000509106.1:p.Gly354=
ENST00000690625.1:n.1377C>T
ENST00000691268.1:c.501C>T
ENST00000691396.1:c.*867C>T	ENSP00000510712.1:n.*867C>T
ENST00000691724.1:c.*31C>T	ENSP00000509255.1:n.*31C>T
ENST00000691779.1:c.*652C>T	ENSP00000508592.1:n.*652C>T
ENST00000691899.1:c.1074C>T	ENSP00000508763.1:p.Gly358=
ENST00000692069.1:n.1640C>T
ENST00000692093.1:c.975C>T	ENSP00000509669.1:p.Gly325=
ENST00000692311.1:n.1898C>T
ENST00000692558.1:n.1439C>T
ENST00000692773.1:c.*811C>T	ENSP00000509055.1:n.*811C>T
ENST00000692830.1:c.*819C>T	ENSP00000509461.1:n.*819C>T
ENST00000693069.1:c.975C>T	ENSP00000510072.1:p.Gly325=
ENST00000693312.1:c.849C>T	ENSP00000508686.1:p.Gly283=
ENST00000693664.1:c.1074C>T	ENSP00000509614.1:p.Gly358=
ENST00000693705.1:c.*751C>T	ENSP00000510697.1:n.*751C>T
ENST00000251849.9:c.1074C>T MANE Select	ENSP00000251849.4:p.Gly358=
ENST00000442415.7:c.1134C>T	ENSP00000401888.2:p.Gly378=
ENST00000251849.8:c.1074C>T	ENSP00000251849.4:p.Gly358=
ENST00000423275.5:c.*751C>T	ENSP00000401088.1:n.*751C>T
ENST00000432427.2:c.711C>T	ENSP00000398591.2:p.Gly237=
ENST00000442415.6:c.1134C>T	ENSP00000401888.2:p.Gly378=
ENST00000460610.1:n.31C>T
ENST00000465826.5:n.318C>T
NM_002880.3:c.1074C>T , LRG_413t1:c.1074C>T	NP_002871.1:p.Gly358=
XM_005265355.1:c.1074C>T	XP_005265412.1:p.Gly358=
XM_005265357.1:c.975C>T	XP_005265414.1:p.Gly325=
XM_005265358.3:c.831C>T	XP_005265415.1:p.Gly277=
XM_005265359.3:c.732C>T	XP_005265416.1:p.Gly244=
XM_005265360.1:c.1074C>T	XP_005265417.1:p.Gly358=
XM_011533974.1:c.1074C>T	XP_011532276.1:p.Gly358=
XM_011533975.1:c.831C>T	XP_011532277.1:p.Gly277=
NM_001354689.1:c.1134C>T	NP_001341618.1:p.Gly378=
NM_001354690.1:c.1074C>T	NP_001341619.1:p.Gly358=
NM_001354691.1:c.831C>T	NP_001341620.1:p.Gly277=
NM_001354692.1:c.831C>T	NP_001341621.1:p.Gly277=
NM_001354693.1:c.975C>T	NP_001341622.1:p.Gly325=
NM_001354694.1:c.891C>T	NP_001341623.1:p.Gly297=
NM_001354695.1:c.732C>T	NP_001341624.1:p.Gly244=
NR_148940.1:n.1489C>T
NR_148941.1:n.1489C>T
NR_148942.1:n.1487C>T
XM_011533974.3:c.1074C>T	XP_011532276.1:p.Gly358=
XM_017006966.1:c.975C>T	XP_016862455.1:p.Gly325=
XR_001740227.1:n.1306C>T
NM_001354689.3:c.1134C>T	NP_001341618.1:p.Gly378=
NM_001354690.2:c.1074C>T	NP_001341619.1:p.Gly358=
NM_001354691.2:c.831C>T	NP_001341620.1:p.Gly277=
NM_001354692.2:c.831C>T	NP_001341621.1:p.Gly277=
NM_001354693.2:c.975C>T	NP_001341622.1:p.Gly325=
NM_001354694.2:c.891C>T	NP_001341623.1:p.Gly297=
NM_001354695.2:c.732C>T	NP_001341624.1:p.Gly244=
NR_148940.2:n.1405C>T
NR_148941.2:n.1405C>T
NR_148942.2:n.1403C>T
NM_001354690.3:c.1074C>T	NP_001341619.1:p.Gly358=
NM_001354691.3:c.831C>T	NP_001341620.1:p.Gly277=
NM_001354692.3:c.831C>T	NP_001341621.1:p.Gly277=
NM_001354693.3:c.975C>T	NP_001341622.1:p.Gly325=
NM_001354694.3:c.891C>T	NP_001341623.1:p.Gly297=
NM_001354695.3:c.732C>T	NP_001341624.1:p.Gly244=
NM_002880.4:c.1074C>T MANE Select	NP_002871.1:p.Gly358=
NR_148940.3:n.1405C>T
NR_148941.3:n.1405C>T
NR_148942.3:n.1403C>T