Canonical Allele Identifier: CA351507379

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12641217C>A (hg19) ; chr3:g.12599718C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12599718C>A , CM000665.2:g.12599718C>A	GRCh38
NC_000003.11:g.12641217C>A , CM000665.1:g.12641217C>A	GRCh37
NC_000003.10:g.12616217C>A	NCBI36
NG_007467.1:g.69462G>T , LRG_413:g.69462G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*746G>T	ENSP00000401088.1:n.*746G>T
ENST00000432427.3:c.401G>T
ENST00000465826.6:n.672G>T
ENST00000491290.2:n.1458G>T
ENST00000684903.1:c.*758G>T	ENSP00000508612.1:n.*758G>T
ENST00000685348.1:c.*758G>T	ENSP00000510285.1:n.*758G>T
ENST00000685437.1:c.982G>T	ENSP00000508794.1:p.Gly328Ter
ENST00000685653.1:c.1081G>T	ENSP00000509968.1:p.Gly361Ter
ENST00000685738.1:c.1081G>T	ENSP00000510156.1:p.Gly361Ter
ENST00000686409.1:n.2132G>T
ENST00000686455.1:n.1444G>T
ENST00000686479.1:n.1452G>T
ENST00000686762.1:c.1081G>T	ENSP00000509767.1:p.Gly361Ter
ENST00000687257.1:n.1317G>T
ENST00000687326.1:c.1081G>T	ENSP00000509665.1:p.Gly361Ter
ENST00000687486.1:c.273G>T
ENST00000687505.1:n.1199G>T
ENST00000687923.1:c.982G>T	ENSP00000510255.1:p.Gly328Ter
ENST00000687940.1:n.1458G>T
ENST00000688269.1:n.1677G>T
ENST00000688326.1:c.401G>T
ENST00000688444.1:n.1407G>T
ENST00000688543.1:c.982G>T	ENSP00000509612.1:p.Gly328Ter
ENST00000688625.1:c.*659G>T	ENSP00000509522.1:n.*659G>T
ENST00000688803.1:n.1312G>T
ENST00000688914.1:n.67G>T
ENST00000689097.1:c.*758G>T	ENSP00000509756.1:n.*758G>T
ENST00000689389.1:c.1081G>T	ENSP00000510213.1:p.Gly361Ter
ENST00000689418.1:c.*758G>T	ENSP00000509467.1:n.*758G>T
ENST00000689481.1:c.*758G>T	ENSP00000510248.1:n.*758G>T
ENST00000689540.1:n.1231G>T
ENST00000689876.1:c.1081G>T	ENSP00000508535.1:p.Gly361Ter
ENST00000689914.1:c.1081G>T	ENSP00000509847.1:p.Gly361Ter
ENST00000690397.1:c.970G>T	ENSP00000508730.1:p.Gly324Ter
ENST00000690460.1:c.1069G>T	ENSP00000509106.1:p.Gly357Ter
ENST00000690625.1:n.1384G>T
ENST00000691268.1:c.508G>T
ENST00000691396.1:c.*874G>T	ENSP00000510712.1:n.*874G>T
ENST00000691724.1:c.*38G>T	ENSP00000509255.1:n.*38G>T
ENST00000691779.1:c.*659G>T	ENSP00000508592.1:n.*659G>T
ENST00000691899.1:c.1081G>T	ENSP00000508763.1:p.Gly361Ter
ENST00000692069.1:n.1647G>T
ENST00000692093.1:c.982G>T	ENSP00000509669.1:p.Gly328Ter
ENST00000692311.1:n.1905G>T
ENST00000692558.1:n.1446G>T
ENST00000692773.1:c.*818G>T	ENSP00000509055.1:n.*818G>T
ENST00000692830.1:c.*826G>T	ENSP00000509461.1:n.*826G>T
ENST00000693069.1:c.982G>T	ENSP00000510072.1:p.Gly328Ter
ENST00000693312.1:c.856G>T	ENSP00000508686.1:p.Gly286Ter
ENST00000693664.1:c.1081G>T	ENSP00000509614.1:p.Gly361Ter
ENST00000693705.1:c.*758G>T	ENSP00000510697.1:n.*758G>T
ENST00000251849.9:c.1081G>T MANE Select	ENSP00000251849.4:p.Gly361Ter
ENST00000442415.7:c.1141G>T	ENSP00000401888.2:p.Gly381Ter
ENST00000251849.8:c.1081G>T	ENSP00000251849.4:p.Gly361Ter
ENST00000423275.5:c.*758G>T	ENSP00000401088.1:n.*758G>T
ENST00000432427.2:c.718G>T	ENSP00000398591.2:p.Gly240Ter
ENST00000442415.6:c.1141G>T	ENSP00000401888.2:p.Gly381Ter
ENST00000460610.1:n.38G>T
ENST00000465826.5:n.325G>T
NM_002880.3:c.1081G>T , LRG_413t1:c.1081G>T	NP_002871.1:p.Gly361Ter
XM_005265355.1:c.1081G>T	XP_005265412.1:p.Gly361Ter
XM_005265357.1:c.982G>T	XP_005265414.1:p.Gly328Ter
XM_005265358.3:c.838G>T	XP_005265415.1:p.Gly280Ter
XM_005265359.3:c.739G>T	XP_005265416.1:p.Gly247Ter
XM_005265360.1:c.1081G>T	XP_005265417.1:p.Gly361Ter
XM_011533974.1:c.1081G>T	XP_011532276.1:p.Gly361Ter
XM_011533975.1:c.838G>T	XP_011532277.1:p.Gly280Ter
NM_001354689.1:c.1141G>T	NP_001341618.1:p.Gly381Ter
NM_001354690.1:c.1081G>T	NP_001341619.1:p.Gly361Ter
NM_001354691.1:c.838G>T	NP_001341620.1:p.Gly280Ter
NM_001354692.1:c.838G>T	NP_001341621.1:p.Gly280Ter
NM_001354693.1:c.982G>T	NP_001341622.1:p.Gly328Ter
NM_001354694.1:c.898G>T	NP_001341623.1:p.Gly300Ter
NM_001354695.1:c.739G>T	NP_001341624.1:p.Gly247Ter
NR_148940.1:n.1496G>T
NR_148941.1:n.1496G>T
NR_148942.1:n.1494G>T
XM_011533974.3:c.1081G>T	XP_011532276.1:p.Gly361Ter
XM_017006966.1:c.982G>T	XP_016862455.1:p.Gly328Ter
XR_001740227.1:n.1313G>T
NM_001354689.3:c.1141G>T	NP_001341618.1:p.Gly381Ter
NM_001354690.2:c.1081G>T	NP_001341619.1:p.Gly361Ter
NM_001354691.2:c.838G>T	NP_001341620.1:p.Gly280Ter
NM_001354692.2:c.838G>T	NP_001341621.1:p.Gly280Ter
NM_001354693.2:c.982G>T	NP_001341622.1:p.Gly328Ter
NM_001354694.2:c.898G>T	NP_001341623.1:p.Gly300Ter
NM_001354695.2:c.739G>T	NP_001341624.1:p.Gly247Ter
NR_148940.2:n.1412G>T
NR_148941.2:n.1412G>T
NR_148942.2:n.1410G>T
NM_001354690.3:c.1081G>T	NP_001341619.1:p.Gly361Ter
NM_001354691.3:c.838G>T	NP_001341620.1:p.Gly280Ter
NM_001354692.3:c.838G>T	NP_001341621.1:p.Gly280Ter
NM_001354693.3:c.982G>T	NP_001341622.1:p.Gly328Ter
NM_001354694.3:c.898G>T	NP_001341623.1:p.Gly300Ter
NM_001354695.3:c.739G>T	NP_001341624.1:p.Gly247Ter
NM_002880.4:c.1081G>T MANE Select	NP_002871.1:p.Gly361Ter
NR_148940.3:n.1412G>T
NR_148941.3:n.1412G>T
NR_148942.3:n.1410G>T