Canonical Allele Identifier: CA69609097

Gene: RAF1

Linked Data

• dbSNP Id: rs11549993
• MyVariant Identifiers: chr3:g.12632470T>C (hg19) ; chr3:g.12590971T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590971T>C , CM000665.2:g.12590971T>C	GRCh38
NC_000003.11:g.12632470T>C , CM000665.1:g.12632470T>C	GRCh37
NC_000003.10:g.12607470T>C	NCBI36
NG_007467.1:g.78209A>G , LRG_413:g.78209A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*862A>G	ENSP00000401088.1:n.*862A>G
ENST00000432427.3:c.514A>G
ENST00000465826.6:n.788A>G
ENST00000475353.2:n.1119A>G
ENST00000494557.2:n.1008A>G
ENST00000684903.1:c.*874A>G	ENSP00000508612.1:n.*874A>G
ENST00000685348.1:c.*874A>G	ENSP00000510285.1:n.*874A>G
ENST00000685437.1:c.1098A>G	ENSP00000508794.1:p.Lys366=
ENST00000685653.1:c.1197A>G	ENSP00000509968.1:p.Lys399=
ENST00000685738.1:c.*161A>G	ENSP00000510156.1:n.*161A>G
ENST00000686409.1:n.2248A>G
ENST00000686455.1:n.1560A>G
ENST00000686762.1:c.1197A>G	ENSP00000509767.1:p.Lys399=
ENST00000687257.1:n.1433A>G
ENST00000687326.1:c.*131A>G	ENSP00000509665.1:n.*131A>G
ENST00000687505.1:n.1315A>G
ENST00000687923.1:c.1086A>G	ENSP00000510255.1:p.Lys362=
ENST00000687940.1:n.1574A>G
ENST00000688269.1:n.1793A>G
ENST00000688326.1:c.630A>G
ENST00000688444.1:n.1523A>G
ENST00000688543.1:c.1098A>G	ENSP00000509612.1:p.Lys366=
ENST00000688625.1:c.*775A>G	ENSP00000509522.1:n.*775A>G
ENST00000688803.1:n.1428A>G
ENST00000688914.1:n.183A>G
ENST00000689097.1:c.*874A>G	ENSP00000509756.1:n.*874A>G
ENST00000689389.1:c.1193+737A>G	ENSP00000510213.1:n.1193+737A>G
ENST00000689418.1:c.*874A>G	ENSP00000509467.1:n.*874A>G
ENST00000689481.1:c.*874A>G	ENSP00000510248.1:n.*874A>G
ENST00000689540.1:n.1347A>G
ENST00000689876.1:c.1197A>G	ENSP00000508535.1:p.Lys399=
ENST00000689914.1:c.*131A>G	ENSP00000509847.1:n.*131A>G
ENST00000690397.1:c.1086A>G	ENSP00000508730.1:p.Lys362=
ENST00000690460.1:c.1185A>G	ENSP00000509106.1:p.Lys395=
ENST00000690585.1:c.89A>G
ENST00000690625.1:n.2233A>G
ENST00000691396.1:c.*1049A>G	ENSP00000510712.1:n.*1049A>G
ENST00000691724.1:c.*154A>G	ENSP00000509255.1:n.*154A>G
ENST00000691779.1:c.*775A>G	ENSP00000508592.1:n.*775A>G
ENST00000691888.1:c.89A>G
ENST00000691899.1:c.1197A>G	ENSP00000508763.1:p.Lys399=
ENST00000692069.1:n.1763A>G
ENST00000692093.1:c.1098A>G	ENSP00000509669.1:p.Lys366=
ENST00000692311.1:n.2021A>G
ENST00000692558.1:n.1562A>G
ENST00000692773.1:c.*934A>G	ENSP00000509055.1:n.*934A>G
ENST00000692830.1:c.*942A>G	ENSP00000509461.1:n.*942A>G
ENST00000693069.1:c.*131A>G	ENSP00000510072.1:n.*131A>G
ENST00000693312.1:c.972A>G	ENSP00000508686.1:p.Lys324=
ENST00000693664.1:c.1197A>G	ENSP00000509614.1:p.Lys399=
ENST00000693705.1:c.*874A>G	ENSP00000510697.1:n.*874A>G
ENST00000251849.9:c.1197A>G MANE Select	ENSP00000251849.4:p.Lys399=
ENST00000442415.7:c.1257A>G	ENSP00000401888.2:p.Lys419=
ENST00000251849.8:c.1197A>G	ENSP00000251849.4:p.Lys399=
ENST00000423275.5:c.*874A>G	ENSP00000401088.1:n.*874A>G
ENST00000432427.2:c.834A>G	ENSP00000398591.2:p.Lys278=
ENST00000442415.6:c.1257A>G	ENSP00000401888.2:p.Lys419=
ENST00000460610.1:n.154A>G
ENST00000465826.5:n.554A>G
ENST00000475353.1:n.365A>G
ENST00000494557.1:n.213A>G
NM_002880.3:c.1197A>G , LRG_413t1:c.1197A>G	NP_002871.1:p.Lys399=
XM_005265355.1:c.1197A>G	XP_005265412.1:p.Lys399=
XM_005265357.1:c.1098A>G	XP_005265414.1:p.Lys366=
XM_005265358.3:c.954A>G	XP_005265415.1:p.Lys318=
XM_005265359.3:c.855A>G	XP_005265416.1:p.Lys285=
XM_005265360.1:c.1197A>G	XP_005265417.1:p.Lys399=
XM_011533974.1:c.1197A>G	XP_011532276.1:p.Lys399=
XM_011533975.1:c.954A>G	XP_011532277.1:p.Lys318=
NM_001354689.1:c.1257A>G	NP_001341618.1:p.Lys419=
NM_001354690.1:c.1197A>G	NP_001341619.1:p.Lys399=
NM_001354691.1:c.954A>G	NP_001341620.1:p.Lys318=
NM_001354692.1:c.954A>G	NP_001341621.1:p.Lys318=
NM_001354693.1:c.1098A>G	NP_001341622.1:p.Lys366=
NM_001354694.1:c.1014A>G	NP_001341623.1:p.Lys338=
NM_001354695.1:c.855A>G	NP_001341624.1:p.Lys285=
NR_148940.1:n.1725A>G
NR_148941.1:n.1671A>G
NR_148942.1:n.1610A>G
XM_011533974.3:c.1197A>G	XP_011532276.1:p.Lys399=
XM_017006966.1:c.1098A>G	XP_016862455.1:p.Lys366=
XR_001740227.1:n.1488A>G
NM_001354689.3:c.1257A>G	NP_001341618.1:p.Lys419=
NM_001354690.2:c.1197A>G	NP_001341619.1:p.Lys399=
NM_001354691.2:c.954A>G	NP_001341620.1:p.Lys318=
NM_001354692.2:c.954A>G	NP_001341621.1:p.Lys318=
NM_001354693.2:c.1098A>G	NP_001341622.1:p.Lys366=
NM_001354694.2:c.1014A>G	NP_001341623.1:p.Lys338=
NM_001354695.2:c.855A>G	NP_001341624.1:p.Lys285=
NR_148940.2:n.1641A>G
NR_148941.2:n.1587A>G
NR_148942.2:n.1526A>G
NM_001354690.3:c.1197A>G	NP_001341619.1:p.Lys399=
NM_001354691.3:c.954A>G	NP_001341620.1:p.Lys318=
NM_001354692.3:c.954A>G	NP_001341621.1:p.Lys318=
NM_001354693.3:c.1098A>G	NP_001341622.1:p.Lys366=
NM_001354694.3:c.1014A>G	NP_001341623.1:p.Lys338=
NM_001354695.3:c.855A>G	NP_001341624.1:p.Lys285=
NM_002880.4:c.1197A>G MANE Select	NP_002871.1:p.Lys399=
NR_148940.3:n.1641A>G
NR_148941.3:n.1587A>G
NR_148942.3:n.1526A>G