Canonical Allele Identifier: CA351501932

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632356C>A (hg19) ; chr3:g.12590857C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590857C>A , CM000665.2:g.12590857C>A	GRCh38
NC_000003.11:g.12632356C>A , CM000665.1:g.12632356C>A	GRCh37
NC_000003.10:g.12607356C>A	NCBI36
NG_007467.1:g.78323G>T , LRG_413:g.78323G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*976G>T	ENSP00000401088.1:n.*976G>T
ENST00000432427.3:c.628G>T
ENST00000460610.2:n.105G>T
ENST00000465826.6:n.902G>T
ENST00000475353.2:n.1233G>T
ENST00000494557.2:n.1122G>T
ENST00000684903.1:c.*988G>T	ENSP00000508612.1:n.*988G>T
ENST00000685348.1:c.*988G>T	ENSP00000510285.1:n.*988G>T
ENST00000685437.1:c.1212G>T	ENSP00000508794.1:p.Glu404Asp
ENST00000685653.1:c.1311G>T	ENSP00000509968.1:p.Glu437Asp
ENST00000685738.1:c.*275G>T	ENSP00000510156.1:n.*275G>T
ENST00000686409.1:n.2362G>T
ENST00000686455.1:n.1674G>T
ENST00000686762.1:c.1311G>T	ENSP00000509767.1:p.Glu437Asp
ENST00000687257.1:n.1547G>T
ENST00000687326.1:c.*245G>T	ENSP00000509665.1:n.*245G>T
ENST00000687505.1:n.1429G>T
ENST00000687923.1:c.1200G>T	ENSP00000510255.1:p.Glu400Asp
ENST00000687940.1:n.1688G>T
ENST00000688269.1:n.1907G>T
ENST00000688326.1:c.744G>T
ENST00000688444.1:n.1637G>T
ENST00000688543.1:c.1212G>T	ENSP00000509612.1:p.Glu404Asp
ENST00000688625.1:c.*889G>T	ENSP00000509522.1:n.*889G>T
ENST00000688803.1:n.1542G>T
ENST00000688914.1:n.297G>T
ENST00000689097.1:c.*988G>T	ENSP00000509756.1:n.*988G>T
ENST00000689389.1:c.1193+851G>T	ENSP00000510213.1:n.1193+851G>T
ENST00000689418.1:c.*988G>T	ENSP00000509467.1:n.*988G>T
ENST00000689481.1:c.*988G>T	ENSP00000510248.1:n.*988G>T
ENST00000689540.1:n.1461G>T
ENST00000689876.1:c.1311G>T	ENSP00000508535.1:p.Glu437Asp
ENST00000689914.1:c.*245G>T	ENSP00000509847.1:n.*245G>T
ENST00000690397.1:c.1200G>T	ENSP00000508730.1:p.Glu400Asp
ENST00000690460.1:c.1299G>T	ENSP00000509106.1:p.Glu433Asp
ENST00000690585.1:c.203G>T
ENST00000690625.1:n.2347G>T
ENST00000691396.1:c.*1163G>T	ENSP00000510712.1:n.*1163G>T
ENST00000691724.1:c.*268G>T	ENSP00000509255.1:n.*268G>T
ENST00000691779.1:c.*889G>T	ENSP00000508592.1:n.*889G>T
ENST00000691888.1:c.203G>T
ENST00000691899.1:c.1311G>T	ENSP00000508763.1:p.Glu437Asp
ENST00000692069.1:n.1877G>T
ENST00000692093.1:c.1212G>T	ENSP00000509669.1:p.Glu404Asp
ENST00000692311.1:n.2135G>T
ENST00000692558.1:n.1676G>T
ENST00000692773.1:c.*1048G>T	ENSP00000509055.1:n.*1048G>T
ENST00000692830.1:c.*1056G>T	ENSP00000509461.1:n.*1056G>T
ENST00000693069.1:c.*245G>T	ENSP00000510072.1:n.*245G>T
ENST00000693312.1:c.1086G>T	ENSP00000508686.1:p.Glu362Asp
ENST00000693664.1:c.1311G>T	ENSP00000509614.1:p.Glu437Asp
ENST00000693705.1:c.*988G>T	ENSP00000510697.1:n.*988G>T
ENST00000251849.9:c.1311G>T MANE Select	ENSP00000251849.4:p.Glu437Asp
ENST00000442415.7:c.1371G>T	ENSP00000401888.2:p.Glu457Asp
ENST00000251849.8:c.1311G>T	ENSP00000251849.4:p.Glu437Asp
ENST00000423275.5:c.*988G>T	ENSP00000401088.1:n.*988G>T
ENST00000432427.2:c.948G>T	ENSP00000398591.2:p.Glu316Asp
ENST00000442415.6:c.1371G>T	ENSP00000401888.2:p.Glu457Asp
ENST00000460610.1:n.268G>T
ENST00000465826.5:n.668G>T
ENST00000475353.1:n.479G>T
ENST00000494557.1:n.327G>T
NM_002880.3:c.1311G>T , LRG_413t1:c.1311G>T	NP_002871.1:p.Glu437Asp
XM_005265355.1:c.1311G>T	XP_005265412.1:p.Glu437Asp
XM_005265357.1:c.1212G>T	XP_005265414.1:p.Glu404Asp
XM_005265358.3:c.1068G>T	XP_005265415.1:p.Glu356Asp
XM_005265359.3:c.969G>T	XP_005265416.1:p.Glu323Asp
XM_005265360.1:c.1311G>T	XP_005265417.1:p.Glu437Asp
XM_011533974.1:c.1311G>T	XP_011532276.1:p.Glu437Asp
XM_011533975.1:c.1068G>T	XP_011532277.1:p.Glu356Asp
NM_001354689.1:c.1371G>T	NP_001341618.1:p.Glu457Asp
NM_001354690.1:c.1311G>T	NP_001341619.1:p.Glu437Asp
NM_001354691.1:c.1068G>T	NP_001341620.1:p.Glu356Asp
NM_001354692.1:c.1068G>T	NP_001341621.1:p.Glu356Asp
NM_001354693.1:c.1212G>T	NP_001341622.1:p.Glu404Asp
NM_001354694.1:c.1128G>T	NP_001341623.1:p.Glu376Asp
NM_001354695.1:c.969G>T	NP_001341624.1:p.Glu323Asp
NR_148940.1:n.1839G>T
NR_148941.1:n.1785G>T
NR_148942.1:n.1724G>T
XM_011533974.3:c.1311G>T	XP_011532276.1:p.Glu437Asp
XM_017006966.1:c.1212G>T	XP_016862455.1:p.Glu404Asp
NM_001354689.3:c.1371G>T	NP_001341618.1:p.Glu457Asp
NM_001354690.2:c.1311G>T	NP_001341619.1:p.Glu437Asp
NM_001354691.2:c.1068G>T	NP_001341620.1:p.Glu356Asp
NM_001354692.2:c.1068G>T	NP_001341621.1:p.Glu356Asp
NM_001354693.2:c.1212G>T	NP_001341622.1:p.Glu404Asp
NM_001354694.2:c.1128G>T	NP_001341623.1:p.Glu376Asp
NM_001354695.2:c.969G>T	NP_001341624.1:p.Glu323Asp
NR_148940.2:n.1755G>T
NR_148941.2:n.1701G>T
NR_148942.2:n.1640G>T
NM_001354690.3:c.1311G>T	NP_001341619.1:p.Glu437Asp
NM_001354691.3:c.1068G>T	NP_001341620.1:p.Glu356Asp
NM_001354692.3:c.1068G>T	NP_001341621.1:p.Glu356Asp
NM_001354693.3:c.1212G>T	NP_001341622.1:p.Glu404Asp
NM_001354694.3:c.1128G>T	NP_001341623.1:p.Glu376Asp
NM_001354695.3:c.969G>T	NP_001341624.1:p.Glu323Asp
NM_002880.4:c.1311G>T MANE Select	NP_002871.1:p.Glu437Asp
NR_148940.3:n.1755G>T
NR_148941.3:n.1701G>T
NR_148942.3:n.1640G>T