Canonical Allele Identifier: CA351502218

Gene: RAF1

Linked Data

• dbSNP Id: rs2125343342
• MyVariant Identifiers: chr3:g.12632399C>T (hg19) ; chr3:g.12590900C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590900C>T , CM000665.2:g.12590900C>T	GRCh38
NC_000003.11:g.12632399C>T , CM000665.1:g.12632399C>T	GRCh37
NC_000003.10:g.12607399C>T	NCBI36
NG_007467.1:g.78280G>A , LRG_413:g.78280G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*933G>A	ENSP00000401088.1:n.*933G>A
ENST00000432427.3:c.585G>A
ENST00000460610.2:n.62G>A
ENST00000465826.6:n.859G>A
ENST00000475353.2:n.1190G>A
ENST00000494557.2:n.1079G>A
ENST00000684903.1:c.*945G>A	ENSP00000508612.1:n.*945G>A
ENST00000685348.1:c.*945G>A	ENSP00000510285.1:n.*945G>A
ENST00000685437.1:c.1169G>A	ENSP00000508794.1:p.Trp390Ter
ENST00000685653.1:c.1268G>A	ENSP00000509968.1:p.Trp423Ter
ENST00000685738.1:c.*232G>A	ENSP00000510156.1:n.*232G>A
ENST00000686409.1:n.2319G>A
ENST00000686455.1:n.1631G>A
ENST00000686762.1:c.1268G>A	ENSP00000509767.1:p.Trp423Ter
ENST00000687257.1:n.1504G>A
ENST00000687326.1:c.*202G>A	ENSP00000509665.1:n.*202G>A
ENST00000687505.1:n.1386G>A
ENST00000687923.1:c.1157G>A	ENSP00000510255.1:p.Trp386Ter
ENST00000687940.1:n.1645G>A
ENST00000688269.1:n.1864G>A
ENST00000688326.1:c.701G>A
ENST00000688444.1:n.1594G>A
ENST00000688543.1:c.1169G>A	ENSP00000509612.1:p.Trp390Ter
ENST00000688625.1:c.*846G>A	ENSP00000509522.1:n.*846G>A
ENST00000688803.1:n.1499G>A
ENST00000688914.1:n.254G>A
ENST00000689097.1:c.*945G>A	ENSP00000509756.1:n.*945G>A
ENST00000689389.1:c.1193+808G>A	ENSP00000510213.1:n.1193+808G>A
ENST00000689418.1:c.*945G>A	ENSP00000509467.1:n.*945G>A
ENST00000689481.1:c.*945G>A	ENSP00000510248.1:n.*945G>A
ENST00000689540.1:n.1418G>A
ENST00000689876.1:c.1268G>A	ENSP00000508535.1:p.Trp423Ter
ENST00000689914.1:c.*202G>A	ENSP00000509847.1:n.*202G>A
ENST00000690397.1:c.1157G>A	ENSP00000508730.1:p.Trp386Ter
ENST00000690460.1:c.1256G>A	ENSP00000509106.1:p.Trp419Ter
ENST00000690585.1:c.160G>A
ENST00000690625.1:n.2304G>A
ENST00000691396.1:c.*1120G>A	ENSP00000510712.1:n.*1120G>A
ENST00000691724.1:c.*225G>A	ENSP00000509255.1:n.*225G>A
ENST00000691779.1:c.*846G>A	ENSP00000508592.1:n.*846G>A
ENST00000691888.1:c.160G>A
ENST00000691899.1:c.1268G>A	ENSP00000508763.1:p.Trp423Ter
ENST00000692069.1:n.1834G>A
ENST00000692093.1:c.1169G>A	ENSP00000509669.1:p.Trp390Ter
ENST00000692311.1:n.2092G>A
ENST00000692558.1:n.1633G>A
ENST00000692773.1:c.*1005G>A	ENSP00000509055.1:n.*1005G>A
ENST00000692830.1:c.*1013G>A	ENSP00000509461.1:n.*1013G>A
ENST00000693069.1:c.*202G>A	ENSP00000510072.1:n.*202G>A
ENST00000693312.1:c.1043G>A	ENSP00000508686.1:p.Trp348Ter
ENST00000693664.1:c.1268G>A	ENSP00000509614.1:p.Trp423Ter
ENST00000693705.1:c.*945G>A	ENSP00000510697.1:n.*945G>A
ENST00000251849.9:c.1268G>A MANE Select	ENSP00000251849.4:p.Trp423Ter
ENST00000442415.7:c.1328G>A	ENSP00000401888.2:p.Trp443Ter
ENST00000251849.8:c.1268G>A	ENSP00000251849.4:p.Trp423Ter
ENST00000423275.5:c.*945G>A	ENSP00000401088.1:n.*945G>A
ENST00000432427.2:c.905G>A	ENSP00000398591.2:p.Trp302Ter
ENST00000442415.6:c.1328G>A	ENSP00000401888.2:p.Trp443Ter
ENST00000460610.1:n.225G>A
ENST00000465826.5:n.625G>A
ENST00000475353.1:n.436G>A
ENST00000494557.1:n.284G>A
NM_002880.3:c.1268G>A , LRG_413t1:c.1268G>A	NP_002871.1:p.Trp423Ter
XM_005265355.1:c.1268G>A	XP_005265412.1:p.Trp423Ter
XM_005265357.1:c.1169G>A	XP_005265414.1:p.Trp390Ter
XM_005265358.3:c.1025G>A	XP_005265415.1:p.Trp342Ter
XM_005265359.3:c.926G>A	XP_005265416.1:p.Trp309Ter
XM_005265360.1:c.1268G>A	XP_005265417.1:p.Trp423Ter
XM_011533974.1:c.1268G>A	XP_011532276.1:p.Trp423Ter
XM_011533975.1:c.1025G>A	XP_011532277.1:p.Trp342Ter
NM_001354689.1:c.1328G>A	NP_001341618.1:p.Trp443Ter
NM_001354690.1:c.1268G>A	NP_001341619.1:p.Trp423Ter
NM_001354691.1:c.1025G>A	NP_001341620.1:p.Trp342Ter
NM_001354692.1:c.1025G>A	NP_001341621.1:p.Trp342Ter
NM_001354693.1:c.1169G>A	NP_001341622.1:p.Trp390Ter
NM_001354694.1:c.1085G>A	NP_001341623.1:p.Trp362Ter
NM_001354695.1:c.926G>A	NP_001341624.1:p.Trp309Ter
NR_148940.1:n.1796G>A
NR_148941.1:n.1742G>A
NR_148942.1:n.1681G>A
XM_011533974.3:c.1268G>A	XP_011532276.1:p.Trp423Ter
XM_017006966.1:c.1169G>A	XP_016862455.1:p.Trp390Ter
NM_001354689.3:c.1328G>A	NP_001341618.1:p.Trp443Ter
NM_001354690.2:c.1268G>A	NP_001341619.1:p.Trp423Ter
NM_001354691.2:c.1025G>A	NP_001341620.1:p.Trp342Ter
NM_001354692.2:c.1025G>A	NP_001341621.1:p.Trp342Ter
NM_001354693.2:c.1169G>A	NP_001341622.1:p.Trp390Ter
NM_001354694.2:c.1085G>A	NP_001341623.1:p.Trp362Ter
NM_001354695.2:c.926G>A	NP_001341624.1:p.Trp309Ter
NR_148940.2:n.1712G>A
NR_148941.2:n.1658G>A
NR_148942.2:n.1597G>A
NM_001354690.3:c.1268G>A	NP_001341619.1:p.Trp423Ter
NM_001354691.3:c.1025G>A	NP_001341620.1:p.Trp342Ter
NM_001354692.3:c.1025G>A	NP_001341621.1:p.Trp342Ter
NM_001354693.3:c.1169G>A	NP_001341622.1:p.Trp390Ter
NM_001354694.3:c.1085G>A	NP_001341623.1:p.Trp362Ter
NM_001354695.3:c.926G>A	NP_001341624.1:p.Trp309Ter
NM_002880.4:c.1268G>A MANE Select	NP_002871.1:p.Trp423Ter
NR_148940.3:n.1712G>A
NR_148941.3:n.1658G>A
NR_148942.3:n.1597G>A