Canonical Allele Identifier: CA351499144

Gene: RAF1 MKRN2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585757A>T , CM000665.2:g.12585757A>T	GRCh38
NC_000003.11:g.12627256A>T , CM000665.1:g.12627256A>T	GRCh37
NC_000003.10:g.12602256A>T	NCBI36
NG_007467.1:g.83423T>A , LRG_413:g.83423T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1125T>A (RAF1)	ENSP00000401088.1:n.*1125T>A
ENST00000432427.3:c.777T>A (RAF1)
ENST00000460610.2:n.5205T>A (RAF1)
ENST00000471449.2:n.270T>A (RAF1)
ENST00000475353.2:n.3173T>A (RAF1)
ENST00000684903.1:c.*1137T>A (RAF1)	ENSP00000508612.1:n.*1137T>A
ENST00000685348.1:c.*1095-351T>A (RAF1)	ENSP00000510285.1:n.*1095-351T>A
ENST00000685437.1:c.1361T>A (RAF1)	ENSP00000508794.1:p.Phe454Tyr
ENST00000685653.1:c.1460T>A (RAF1)	ENSP00000509968.1:p.Phe487Tyr
ENST00000685697.1:n.2195T>A (RAF1)
ENST00000685738.1:c.*424T>A (RAF1)	ENSP00000510156.1:n.*424T>A
ENST00000686409.1:n.4302T>A (RAF1)
ENST00000686455.1:n.3614T>A (RAF1)
ENST00000686762.1:c.*19T>A (RAF1)	ENSP00000509767.1:n.*19T>A
ENST00000687257.1:n.3487T>A (RAF1)
ENST00000687326.1:c.*2185T>A (RAF1)	ENSP00000509665.1:n.*2185T>A
ENST00000687505.1:n.1578T>A (RAF1)
ENST00000687923.1:c.1349T>A (RAF1)	ENSP00000510255.1:p.Phe450Tyr
ENST00000688269.1:n.2056T>A (RAF1)
ENST00000688444.1:n.3577T>A (RAF1)
ENST00000688543.1:c.1361T>A (RAF1)	ENSP00000509612.1:p.Phe454Tyr
ENST00000688625.1:c.*2829T>A (RAF1)	ENSP00000509522.1:n.*2829T>A
ENST00000688803.1:n.2965-504T>A (RAF1)
ENST00000688914.1:n.446T>A (RAF1)
ENST00000689097.1:c.*1137T>A (RAF1)	ENSP00000509756.1:n.*1137T>A
ENST00000689389.1:c.1283T>A (RAF1)	ENSP00000510213.1:p.Phe428Tyr
ENST00000689418.1:c.*2928T>A (RAF1)	ENSP00000509467.1:n.*2928T>A
ENST00000689540.1:n.3401T>A (RAF1)
ENST00000689876.1:c.1418-351T>A (RAF1)	ENSP00000508535.1:n.1418-351T>A
ENST00000689914.1:c.*394T>A (RAF1)	ENSP00000509847.1:n.*394T>A
ENST00000690397.1:c.1349T>A (RAF1)	ENSP00000508730.1:p.Phe450Tyr
ENST00000690460.1:c.1448T>A (RAF1)	ENSP00000509106.1:p.Phe483Tyr
ENST00000690585.1:c.263-504T>A (RAF1)
ENST00000690625.1:n.2496T>A (RAF1)
ENST00000691396.1:c.*1332T>A (RAF1)	ENSP00000510712.1:n.*1332T>A
ENST00000691643.1:n.2086T>A (RAF1)
ENST00000691724.1:c.*417T>A (RAF1)	ENSP00000509255.1:n.*417T>A
ENST00000691779.1:c.*1038T>A (RAF1)	ENSP00000508592.1:n.*1038T>A
ENST00000691888.1:c.334T>A (RAF1)
ENST00000691899.1:c.1460T>A (RAF1)	ENSP00000508763.1:p.Phe487Tyr
ENST00000692069.1:n.3817T>A (RAF1)
ENST00000692093.1:c.1361T>A (RAF1)	ENSP00000509669.1:p.Phe454Tyr
ENST00000692311.1:n.2284T>A (RAF1)
ENST00000692558.1:n.3616T>A (RAF1)
ENST00000692773.1:c.*1197T>A (RAF1)	ENSP00000509055.1:n.*1197T>A
ENST00000692830.1:c.*1205T>A (RAF1)	ENSP00000509461.1:n.*1205T>A
ENST00000693312.1:c.1235T>A (RAF1)	ENSP00000508686.1:p.Phe412Tyr
ENST00000693664.1:c.1488-504T>A (RAF1)	ENSP00000509614.1:n.1488-504T>A
ENST00000693705.1:c.*1048-776T>A (RAF1)	ENSP00000510697.1:n.*1048-776T>A
ENST00000251849.9:c.1460T>A (RAF1) MANE Select	ENSP00000251849.4:p.Phe487Tyr
ENST00000442415.7:c.1520T>A (RAF1)	ENSP00000401888.2:p.Phe507Tyr
ENST00000676541.1:c.*3504A>T (MKRN2)	ENSP00000503730.1:n.*3504A>T
ENST00000677142.1:c.*3504A>T (MKRN2)	ENSP00000504455.1:n.*3504A>T
ENST00000677816.1:c.*2059A>T (MKRN2)	ENSP00000502893.1:n.*2059A>T
ENST00000677941.1:n.3567A>T (MKRN2)
ENST00000251849.8:c.1460T>A (RAF1)	ENSP00000251849.4:p.Phe487Tyr
ENST00000423275.5:c.*1137T>A (RAF1)	ENSP00000401088.1:n.*1137T>A
ENST00000432427.2:c.1097T>A (RAF1)	ENSP00000398591.2:p.Phe366Tyr
ENST00000442415.6:c.1520T>A (RAF1)	ENSP00000401888.2:p.Phe507Tyr
ENST00000471449.1:n.149T>A (RAF1)
NM_002880.3:c.1460T>A , LRG_413t1:c.1460T>A (RAF1)	NP_002871.1:p.Phe487Tyr
XM_005265355.1:c.1460T>A (RAF1)	XP_005265412.1:p.Phe487Tyr
XM_005265357.1:c.1361T>A (RAF1)	XP_005265414.1:p.Phe454Tyr
XM_005265358.3:c.1217T>A (RAF1)	XP_005265415.1:p.Phe406Tyr
XM_005265359.3:c.1118T>A (RAF1)	XP_005265416.1:p.Phe373Tyr
XM_005265360.1:c.1418-351T>A (RAF1)	XP_005265417.1:n.1418-351T>A
XM_011533974.1:c.1460T>A (RAF1)	XP_011532276.1:p.Phe487Tyr
XM_011533975.1:c.1217T>A (RAF1)	XP_011532277.1:p.Phe406Tyr
NM_001354689.1:c.1520T>A (RAF1)	NP_001341618.1:p.Phe507Tyr
NM_001354690.1:c.1460T>A (RAF1)	NP_001341619.1:p.Phe487Tyr
NM_001354691.1:c.1217T>A (RAF1)	NP_001341620.1:p.Phe406Tyr
NM_001354692.1:c.1217T>A (RAF1)	NP_001341621.1:p.Phe406Tyr
NM_001354693.1:c.1361T>A (RAF1)	NP_001341622.1:p.Phe454Tyr
NM_001354694.1:c.1277T>A (RAF1)	NP_001341623.1:p.Phe426Tyr
NM_001354695.1:c.1118T>A (RAF1)	NP_001341624.1:p.Phe373Tyr
NR_148940.1:n.1988T>A (RAF1)
NR_148941.1:n.1934T>A (RAF1)
NR_148942.1:n.1873T>A (RAF1)
XM_011533974.3:c.1460T>A (RAF1)	XP_011532276.1:p.Phe487Tyr
XM_017006966.1:c.1361T>A (RAF1)	XP_016862455.1:p.Phe454Tyr
NM_001354689.3:c.1520T>A (RAF1)	NP_001341618.1:p.Phe507Tyr
NM_001354690.2:c.1460T>A (RAF1)	NP_001341619.1:p.Phe487Tyr
NM_001354691.2:c.1217T>A (RAF1)	NP_001341620.1:p.Phe406Tyr
NM_001354692.2:c.1217T>A (RAF1)	NP_001341621.1:p.Phe406Tyr
NM_001354693.2:c.1361T>A (RAF1)	NP_001341622.1:p.Phe454Tyr
NM_001354694.2:c.1277T>A (RAF1)	NP_001341623.1:p.Phe426Tyr
NM_001354695.2:c.1118T>A (RAF1)	NP_001341624.1:p.Phe373Tyr
NR_148940.2:n.1904T>A (RAF1)
NR_148941.2:n.1850T>A (RAF1)
NR_148942.2:n.1789T>A (RAF1)
NM_001354690.3:c.1460T>A (RAF1)	NP_001341619.1:p.Phe487Tyr
NM_001354691.3:c.1217T>A (RAF1)	NP_001341620.1:p.Phe406Tyr
NM_001354692.3:c.1217T>A (RAF1)	NP_001341621.1:p.Phe406Tyr
NM_001354693.3:c.1361T>A (RAF1)	NP_001341622.1:p.Phe454Tyr
NM_001354694.3:c.1277T>A (RAF1)	NP_001341623.1:p.Phe426Tyr
NM_001354695.3:c.1118T>A (RAF1)	NP_001341624.1:p.Phe373Tyr
NM_002880.4:c.1460T>A (RAF1) MANE Select	NP_002871.1:p.Phe487Tyr
NR_148940.3:n.1904T>A (RAF1)
NR_148941.3:n.1850T>A (RAF1)
NR_148942.3:n.1789T>A (RAF1)