Canonical Allele Identifier: CA351502022

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632373G>A (hg19) ; chr3:g.12590874G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590874G>A , CM000665.2:g.12590874G>A	GRCh38
NC_000003.11:g.12632373G>A , CM000665.1:g.12632373G>A	GRCh37
NC_000003.10:g.12607373G>A	NCBI36
NG_007467.1:g.78306C>T , LRG_413:g.78306C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*959C>T	ENSP00000401088.1:n.*959C>T
ENST00000432427.3:c.611C>T
ENST00000460610.2:n.88C>T
ENST00000465826.6:n.885C>T
ENST00000475353.2:n.1216C>T
ENST00000494557.2:n.1105C>T
ENST00000684903.1:c.*971C>T	ENSP00000508612.1:n.*971C>T
ENST00000685348.1:c.*971C>T	ENSP00000510285.1:n.*971C>T
ENST00000685437.1:c.1195C>T	ENSP00000508794.1:p.His399Tyr
ENST00000685653.1:c.1294C>T	ENSP00000509968.1:p.His432Tyr
ENST00000685738.1:c.*258C>T	ENSP00000510156.1:n.*258C>T
ENST00000686409.1:n.2345C>T
ENST00000686455.1:n.1657C>T
ENST00000686762.1:c.1294C>T	ENSP00000509767.1:p.His432Tyr
ENST00000687257.1:n.1530C>T
ENST00000687326.1:c.*228C>T	ENSP00000509665.1:n.*228C>T
ENST00000687505.1:n.1412C>T
ENST00000687923.1:c.1183C>T	ENSP00000510255.1:p.His395Tyr
ENST00000687940.1:n.1671C>T
ENST00000688269.1:n.1890C>T
ENST00000688326.1:c.727C>T
ENST00000688444.1:n.1620C>T
ENST00000688543.1:c.1195C>T	ENSP00000509612.1:p.His399Tyr
ENST00000688625.1:c.*872C>T	ENSP00000509522.1:n.*872C>T
ENST00000688803.1:n.1525C>T
ENST00000688914.1:n.280C>T
ENST00000689097.1:c.*971C>T	ENSP00000509756.1:n.*971C>T
ENST00000689389.1:c.1193+834C>T	ENSP00000510213.1:n.1193+834C>T
ENST00000689418.1:c.*971C>T	ENSP00000509467.1:n.*971C>T
ENST00000689481.1:c.*971C>T	ENSP00000510248.1:n.*971C>T
ENST00000689540.1:n.1444C>T
ENST00000689876.1:c.1294C>T	ENSP00000508535.1:p.His432Tyr
ENST00000689914.1:c.*228C>T	ENSP00000509847.1:n.*228C>T
ENST00000690397.1:c.1183C>T	ENSP00000508730.1:p.His395Tyr
ENST00000690460.1:c.1282C>T	ENSP00000509106.1:p.His428Tyr
ENST00000690585.1:c.186C>T
ENST00000690625.1:n.2330C>T
ENST00000691396.1:c.*1146C>T	ENSP00000510712.1:n.*1146C>T
ENST00000691724.1:c.*251C>T	ENSP00000509255.1:n.*251C>T
ENST00000691779.1:c.*872C>T	ENSP00000508592.1:n.*872C>T
ENST00000691888.1:c.186C>T
ENST00000691899.1:c.1294C>T	ENSP00000508763.1:p.His432Tyr
ENST00000692069.1:n.1860C>T
ENST00000692093.1:c.1195C>T	ENSP00000509669.1:p.His399Tyr
ENST00000692311.1:n.2118C>T
ENST00000692558.1:n.1659C>T
ENST00000692773.1:c.*1031C>T	ENSP00000509055.1:n.*1031C>T
ENST00000692830.1:c.*1039C>T	ENSP00000509461.1:n.*1039C>T
ENST00000693069.1:c.*228C>T	ENSP00000510072.1:n.*228C>T
ENST00000693312.1:c.1069C>T	ENSP00000508686.1:p.His357Tyr
ENST00000693664.1:c.1294C>T	ENSP00000509614.1:p.His432Tyr
ENST00000693705.1:c.*971C>T	ENSP00000510697.1:n.*971C>T
ENST00000251849.9:c.1294C>T MANE Select	ENSP00000251849.4:p.His432Tyr
ENST00000442415.7:c.1354C>T	ENSP00000401888.2:p.His452Tyr
ENST00000251849.8:c.1294C>T	ENSP00000251849.4:p.His432Tyr
ENST00000423275.5:c.*971C>T	ENSP00000401088.1:n.*971C>T
ENST00000432427.2:c.931C>T	ENSP00000398591.2:p.His311Tyr
ENST00000442415.6:c.1354C>T	ENSP00000401888.2:p.His452Tyr
ENST00000460610.1:n.251C>T
ENST00000465826.5:n.651C>T
ENST00000475353.1:n.462C>T
ENST00000494557.1:n.310C>T
NM_002880.3:c.1294C>T , LRG_413t1:c.1294C>T	NP_002871.1:p.His432Tyr
XM_005265355.1:c.1294C>T	XP_005265412.1:p.His432Tyr
XM_005265357.1:c.1195C>T	XP_005265414.1:p.His399Tyr
XM_005265358.3:c.1051C>T	XP_005265415.1:p.His351Tyr
XM_005265359.3:c.952C>T	XP_005265416.1:p.His318Tyr
XM_005265360.1:c.1294C>T	XP_005265417.1:p.His432Tyr
XM_011533974.1:c.1294C>T	XP_011532276.1:p.His432Tyr
XM_011533975.1:c.1051C>T	XP_011532277.1:p.His351Tyr
NM_001354689.1:c.1354C>T	NP_001341618.1:p.His452Tyr
NM_001354690.1:c.1294C>T	NP_001341619.1:p.His432Tyr
NM_001354691.1:c.1051C>T	NP_001341620.1:p.His351Tyr
NM_001354692.1:c.1051C>T	NP_001341621.1:p.His351Tyr
NM_001354693.1:c.1195C>T	NP_001341622.1:p.His399Tyr
NM_001354694.1:c.1111C>T	NP_001341623.1:p.His371Tyr
NM_001354695.1:c.952C>T	NP_001341624.1:p.His318Tyr
NR_148940.1:n.1822C>T
NR_148941.1:n.1768C>T
NR_148942.1:n.1707C>T
XM_011533974.3:c.1294C>T	XP_011532276.1:p.His432Tyr
XM_017006966.1:c.1195C>T	XP_016862455.1:p.His399Tyr
NM_001354689.3:c.1354C>T	NP_001341618.1:p.His452Tyr
NM_001354690.2:c.1294C>T	NP_001341619.1:p.His432Tyr
NM_001354691.2:c.1051C>T	NP_001341620.1:p.His351Tyr
NM_001354692.2:c.1051C>T	NP_001341621.1:p.His351Tyr
NM_001354693.2:c.1195C>T	NP_001341622.1:p.His399Tyr
NM_001354694.2:c.1111C>T	NP_001341623.1:p.His371Tyr
NM_001354695.2:c.952C>T	NP_001341624.1:p.His318Tyr
NR_148940.2:n.1738C>T
NR_148941.2:n.1684C>T
NR_148942.2:n.1623C>T
NM_001354690.3:c.1294C>T	NP_001341619.1:p.His432Tyr
NM_001354691.3:c.1051C>T	NP_001341620.1:p.His351Tyr
NM_001354692.3:c.1051C>T	NP_001341621.1:p.His351Tyr
NM_001354693.3:c.1195C>T	NP_001341622.1:p.His399Tyr
NM_001354694.3:c.1111C>T	NP_001341623.1:p.His371Tyr
NM_001354695.3:c.952C>T	NP_001341624.1:p.His318Tyr
NM_002880.4:c.1294C>T MANE Select	NP_002871.1:p.His432Tyr
NR_148940.3:n.1738C>T
NR_148941.3:n.1684C>T
NR_148942.3:n.1623C>T