Canonical Allele Identifier: CA351502728

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632472T>C (hg19) ; chr3:g.12590973T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590973T>C , CM000665.2:g.12590973T>C	GRCh38
NC_000003.11:g.12632472T>C , CM000665.1:g.12632472T>C	GRCh37
NC_000003.10:g.12607472T>C	NCBI36
NG_007467.1:g.78207A>G , LRG_413:g.78207A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*860A>G	ENSP00000401088.1:n.*860A>G
ENST00000432427.3:c.512A>G
ENST00000465826.6:n.786A>G
ENST00000475353.2:n.1117A>G
ENST00000494557.2:n.1006A>G
ENST00000684903.1:c.*872A>G	ENSP00000508612.1:n.*872A>G
ENST00000685348.1:c.*872A>G	ENSP00000510285.1:n.*872A>G
ENST00000685437.1:c.1096A>G	ENSP00000508794.1:p.Lys366Glu
ENST00000685653.1:c.1195A>G	ENSP00000509968.1:p.Lys399Glu
ENST00000685738.1:c.*159A>G	ENSP00000510156.1:n.*159A>G
ENST00000686409.1:n.2246A>G
ENST00000686455.1:n.1558A>G
ENST00000686762.1:c.1195A>G	ENSP00000509767.1:p.Lys399Glu
ENST00000687257.1:n.1431A>G
ENST00000687326.1:c.*129A>G	ENSP00000509665.1:n.*129A>G
ENST00000687505.1:n.1313A>G
ENST00000687923.1:c.1084A>G	ENSP00000510255.1:p.Lys362Glu
ENST00000687940.1:n.1572A>G
ENST00000688269.1:n.1791A>G
ENST00000688326.1:c.628A>G
ENST00000688444.1:n.1521A>G
ENST00000688543.1:c.1096A>G	ENSP00000509612.1:p.Lys366Glu
ENST00000688625.1:c.*773A>G	ENSP00000509522.1:n.*773A>G
ENST00000688803.1:n.1426A>G
ENST00000688914.1:n.181A>G
ENST00000689097.1:c.*872A>G	ENSP00000509756.1:n.*872A>G
ENST00000689389.1:c.1193+735A>G	ENSP00000510213.1:n.1193+735A>G
ENST00000689418.1:c.*872A>G	ENSP00000509467.1:n.*872A>G
ENST00000689481.1:c.*872A>G	ENSP00000510248.1:n.*872A>G
ENST00000689540.1:n.1345A>G
ENST00000689876.1:c.1195A>G	ENSP00000508535.1:p.Lys399Glu
ENST00000689914.1:c.*129A>G	ENSP00000509847.1:n.*129A>G
ENST00000690397.1:c.1084A>G	ENSP00000508730.1:p.Lys362Glu
ENST00000690460.1:c.1183A>G	ENSP00000509106.1:p.Lys395Glu
ENST00000690585.1:c.87A>G
ENST00000690625.1:n.2231A>G
ENST00000691396.1:c.*1047A>G	ENSP00000510712.1:n.*1047A>G
ENST00000691724.1:c.*152A>G	ENSP00000509255.1:n.*152A>G
ENST00000691779.1:c.*773A>G	ENSP00000508592.1:n.*773A>G
ENST00000691888.1:c.87A>G
ENST00000691899.1:c.1195A>G	ENSP00000508763.1:p.Lys399Glu
ENST00000692069.1:n.1761A>G
ENST00000692093.1:c.1096A>G	ENSP00000509669.1:p.Lys366Glu
ENST00000692311.1:n.2019A>G
ENST00000692558.1:n.1560A>G
ENST00000692773.1:c.*932A>G	ENSP00000509055.1:n.*932A>G
ENST00000692830.1:c.*940A>G	ENSP00000509461.1:n.*940A>G
ENST00000693069.1:c.*129A>G	ENSP00000510072.1:n.*129A>G
ENST00000693312.1:c.970A>G	ENSP00000508686.1:p.Lys324Glu
ENST00000693664.1:c.1195A>G	ENSP00000509614.1:p.Lys399Glu
ENST00000693705.1:c.*872A>G	ENSP00000510697.1:n.*872A>G
ENST00000251849.9:c.1195A>G MANE Select	ENSP00000251849.4:p.Lys399Glu
ENST00000442415.7:c.1255A>G	ENSP00000401888.2:p.Lys419Glu
ENST00000251849.8:c.1195A>G	ENSP00000251849.4:p.Lys399Glu
ENST00000423275.5:c.*872A>G	ENSP00000401088.1:n.*872A>G
ENST00000432427.2:c.832A>G	ENSP00000398591.2:p.Lys278Glu
ENST00000442415.6:c.1255A>G	ENSP00000401888.2:p.Lys419Glu
ENST00000460610.1:n.152A>G
ENST00000465826.5:n.552A>G
ENST00000475353.1:n.363A>G
ENST00000494557.1:n.211A>G
NM_002880.3:c.1195A>G , LRG_413t1:c.1195A>G	NP_002871.1:p.Lys399Glu
XM_005265355.1:c.1195A>G	XP_005265412.1:p.Lys399Glu
XM_005265357.1:c.1096A>G	XP_005265414.1:p.Lys366Glu
XM_005265358.3:c.952A>G	XP_005265415.1:p.Lys318Glu
XM_005265359.3:c.853A>G	XP_005265416.1:p.Lys285Glu
XM_005265360.1:c.1195A>G	XP_005265417.1:p.Lys399Glu
XM_011533974.1:c.1195A>G	XP_011532276.1:p.Lys399Glu
XM_011533975.1:c.952A>G	XP_011532277.1:p.Lys318Glu
NM_001354689.1:c.1255A>G	NP_001341618.1:p.Lys419Glu
NM_001354690.1:c.1195A>G	NP_001341619.1:p.Lys399Glu
NM_001354691.1:c.952A>G	NP_001341620.1:p.Lys318Glu
NM_001354692.1:c.952A>G	NP_001341621.1:p.Lys318Glu
NM_001354693.1:c.1096A>G	NP_001341622.1:p.Lys366Glu
NM_001354694.1:c.1012A>G	NP_001341623.1:p.Lys338Glu
NM_001354695.1:c.853A>G	NP_001341624.1:p.Lys285Glu
NR_148940.1:n.1723A>G
NR_148941.1:n.1669A>G
NR_148942.1:n.1608A>G
XM_011533974.3:c.1195A>G	XP_011532276.1:p.Lys399Glu
XM_017006966.1:c.1096A>G	XP_016862455.1:p.Lys366Glu
XR_001740227.1:n.1486A>G
NM_001354689.3:c.1255A>G	NP_001341618.1:p.Lys419Glu
NM_001354690.2:c.1195A>G	NP_001341619.1:p.Lys399Glu
NM_001354691.2:c.952A>G	NP_001341620.1:p.Lys318Glu
NM_001354692.2:c.952A>G	NP_001341621.1:p.Lys318Glu
NM_001354693.2:c.1096A>G	NP_001341622.1:p.Lys366Glu
NM_001354694.2:c.1012A>G	NP_001341623.1:p.Lys338Glu
NM_001354695.2:c.853A>G	NP_001341624.1:p.Lys285Glu
NR_148940.2:n.1639A>G
NR_148941.2:n.1585A>G
NR_148942.2:n.1524A>G
NM_001354690.3:c.1195A>G	NP_001341619.1:p.Lys399Glu
NM_001354691.3:c.952A>G	NP_001341620.1:p.Lys318Glu
NM_001354692.3:c.952A>G	NP_001341621.1:p.Lys318Glu
NM_001354693.3:c.1096A>G	NP_001341622.1:p.Lys366Glu
NM_001354694.3:c.1012A>G	NP_001341623.1:p.Lys338Glu
NM_001354695.3:c.853A>G	NP_001341624.1:p.Lys285Glu
NM_002880.4:c.1195A>G MANE Select	NP_002871.1:p.Lys399Glu
NR_148940.3:n.1639A>G
NR_148941.3:n.1585A>G
NR_148942.3:n.1524A>G