Canonical Allele Identifier: CA351502188

Gene: RAF1

Linked Data

• ClinVar Variation Id: 1765590
• ClinVar RCV Id: RCV002378490
• MyVariant Identifiers: chr3:g.12632396C>T (hg19) ; chr3:g.12590897C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590897C>T , CM000665.2:g.12590897C>T	GRCh38
NC_000003.11:g.12632396C>T , CM000665.1:g.12632396C>T	GRCh37
NC_000003.10:g.12607396C>T	NCBI36
NG_007467.1:g.78283G>A , LRG_413:g.78283G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*936G>A	ENSP00000401088.1:n.*936G>A
ENST00000432427.3:c.588G>A
ENST00000460610.2:n.65G>A
ENST00000465826.6:n.862G>A
ENST00000475353.2:n.1193G>A
ENST00000494557.2:n.1082G>A
ENST00000684903.1:c.*948G>A	ENSP00000508612.1:n.*948G>A
ENST00000685348.1:c.*948G>A	ENSP00000510285.1:n.*948G>A
ENST00000685437.1:c.1172G>A	ENSP00000508794.1:p.Cys391Tyr
ENST00000685653.1:c.1271G>A	ENSP00000509968.1:p.Cys424Tyr
ENST00000685738.1:c.*235G>A	ENSP00000510156.1:n.*235G>A
ENST00000686409.1:n.2322G>A
ENST00000686455.1:n.1634G>A
ENST00000686762.1:c.1271G>A	ENSP00000509767.1:p.Cys424Tyr
ENST00000687257.1:n.1507G>A
ENST00000687326.1:c.*205G>A	ENSP00000509665.1:n.*205G>A
ENST00000687505.1:n.1389G>A
ENST00000687923.1:c.1160G>A	ENSP00000510255.1:p.Cys387Tyr
ENST00000687940.1:n.1648G>A
ENST00000688269.1:n.1867G>A
ENST00000688326.1:c.704G>A
ENST00000688444.1:n.1597G>A
ENST00000688543.1:c.1172G>A	ENSP00000509612.1:p.Cys391Tyr
ENST00000688625.1:c.*849G>A	ENSP00000509522.1:n.*849G>A
ENST00000688803.1:n.1502G>A
ENST00000688914.1:n.257G>A
ENST00000689097.1:c.*948G>A	ENSP00000509756.1:n.*948G>A
ENST00000689389.1:c.1193+811G>A	ENSP00000510213.1:n.1193+811G>A
ENST00000689418.1:c.*948G>A	ENSP00000509467.1:n.*948G>A
ENST00000689481.1:c.*948G>A	ENSP00000510248.1:n.*948G>A
ENST00000689540.1:n.1421G>A
ENST00000689876.1:c.1271G>A	ENSP00000508535.1:p.Cys424Tyr
ENST00000689914.1:c.*205G>A	ENSP00000509847.1:n.*205G>A
ENST00000690397.1:c.1160G>A	ENSP00000508730.1:p.Cys387Tyr
ENST00000690460.1:c.1259G>A	ENSP00000509106.1:p.Cys420Tyr
ENST00000690585.1:c.163G>A
ENST00000690625.1:n.2307G>A
ENST00000691396.1:c.*1123G>A	ENSP00000510712.1:n.*1123G>A
ENST00000691724.1:c.*228G>A	ENSP00000509255.1:n.*228G>A
ENST00000691779.1:c.*849G>A	ENSP00000508592.1:n.*849G>A
ENST00000691888.1:c.163G>A
ENST00000691899.1:c.1271G>A	ENSP00000508763.1:p.Cys424Tyr
ENST00000692069.1:n.1837G>A
ENST00000692093.1:c.1172G>A	ENSP00000509669.1:p.Cys391Tyr
ENST00000692311.1:n.2095G>A
ENST00000692558.1:n.1636G>A
ENST00000692773.1:c.*1008G>A	ENSP00000509055.1:n.*1008G>A
ENST00000692830.1:c.*1016G>A	ENSP00000509461.1:n.*1016G>A
ENST00000693069.1:c.*205G>A	ENSP00000510072.1:n.*205G>A
ENST00000693312.1:c.1046G>A	ENSP00000508686.1:p.Cys349Tyr
ENST00000693664.1:c.1271G>A	ENSP00000509614.1:p.Cys424Tyr
ENST00000693705.1:c.*948G>A	ENSP00000510697.1:n.*948G>A
ENST00000251849.9:c.1271G>A MANE Select	ENSP00000251849.4:p.Cys424Tyr
ENST00000442415.7:c.1331G>A	ENSP00000401888.2:p.Cys444Tyr
ENST00000251849.8:c.1271G>A	ENSP00000251849.4:p.Cys424Tyr
ENST00000423275.5:c.*948G>A	ENSP00000401088.1:n.*948G>A
ENST00000432427.2:c.908G>A	ENSP00000398591.2:p.Cys303Tyr
ENST00000442415.6:c.1331G>A	ENSP00000401888.2:p.Cys444Tyr
ENST00000460610.1:n.228G>A
ENST00000465826.5:n.628G>A
ENST00000475353.1:n.439G>A
ENST00000494557.1:n.287G>A
NM_002880.3:c.1271G>A , LRG_413t1:c.1271G>A	NP_002871.1:p.Cys424Tyr
XM_005265355.1:c.1271G>A	XP_005265412.1:p.Cys424Tyr
XM_005265357.1:c.1172G>A	XP_005265414.1:p.Cys391Tyr
XM_005265358.3:c.1028G>A	XP_005265415.1:p.Cys343Tyr
XM_005265359.3:c.929G>A	XP_005265416.1:p.Cys310Tyr
XM_005265360.1:c.1271G>A	XP_005265417.1:p.Cys424Tyr
XM_011533974.1:c.1271G>A	XP_011532276.1:p.Cys424Tyr
XM_011533975.1:c.1028G>A	XP_011532277.1:p.Cys343Tyr
NM_001354689.1:c.1331G>A	NP_001341618.1:p.Cys444Tyr
NM_001354690.1:c.1271G>A	NP_001341619.1:p.Cys424Tyr
NM_001354691.1:c.1028G>A	NP_001341620.1:p.Cys343Tyr
NM_001354692.1:c.1028G>A	NP_001341621.1:p.Cys343Tyr
NM_001354693.1:c.1172G>A	NP_001341622.1:p.Cys391Tyr
NM_001354694.1:c.1088G>A	NP_001341623.1:p.Cys363Tyr
NM_001354695.1:c.929G>A	NP_001341624.1:p.Cys310Tyr
NR_148940.1:n.1799G>A
NR_148941.1:n.1745G>A
NR_148942.1:n.1684G>A
XM_011533974.3:c.1271G>A	XP_011532276.1:p.Cys424Tyr
XM_017006966.1:c.1172G>A	XP_016862455.1:p.Cys391Tyr
NM_001354689.3:c.1331G>A	NP_001341618.1:p.Cys444Tyr
NM_001354690.2:c.1271G>A	NP_001341619.1:p.Cys424Tyr
NM_001354691.2:c.1028G>A	NP_001341620.1:p.Cys343Tyr
NM_001354692.2:c.1028G>A	NP_001341621.1:p.Cys343Tyr
NM_001354693.2:c.1172G>A	NP_001341622.1:p.Cys391Tyr
NM_001354694.2:c.1088G>A	NP_001341623.1:p.Cys363Tyr
NM_001354695.2:c.929G>A	NP_001341624.1:p.Cys310Tyr
NR_148940.2:n.1715G>A
NR_148941.2:n.1661G>A
NR_148942.2:n.1600G>A
NM_001354690.3:c.1271G>A	NP_001341619.1:p.Cys424Tyr
NM_001354691.3:c.1028G>A	NP_001341620.1:p.Cys343Tyr
NM_001354692.3:c.1028G>A	NP_001341621.1:p.Cys343Tyr
NM_001354693.3:c.1172G>A	NP_001341622.1:p.Cys391Tyr
NM_001354694.3:c.1088G>A	NP_001341623.1:p.Cys363Tyr
NM_001354695.3:c.929G>A	NP_001341624.1:p.Cys310Tyr
NM_002880.4:c.1271G>A MANE Select	NP_002871.1:p.Cys424Tyr
NR_148940.3:n.1715G>A
NR_148941.3:n.1661G>A
NR_148942.3:n.1600G>A