Canonical Allele Identifier: CA1346227857

Gene: RAF1 MKRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585745G= , CM000665.2:g.12585745G=	GRCh38
NC_000003.11:g.12627244G= , CM000665.1:g.12627244G=	GRCh37
NC_000003.10:g.12602244G=	NCBI36
NG_007467.1:g.83435C= , LRG_413:g.83435C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1137C= (RAF1)	ENSP00000401088.1:n.*1137C=
ENST00000432427.3:c.789C= (RAF1)
ENST00000460610.2:n.5217C= (RAF1)
ENST00000471449.2:n.282C= (RAF1)
ENST00000475353.2:n.3185C= (RAF1)
ENST00000684903.1:c.*1149C= (RAF1)	ENSP00000508612.1:n.*1149C=
ENST00000685348.1:c.*1095-339C= (RAF1)	ENSP00000510285.1:n.*1095-339C=
ENST00000685437.1:c.1373C= (RAF1)	ENSP00000508794.1:p.Thr458=
ENST00000685653.1:c.1472C= (RAF1)	ENSP00000509968.1:p.Thr491=
ENST00000685697.1:n.2207C= (RAF1)
ENST00000685738.1:c.*436C= (RAF1)	ENSP00000510156.1:n.*436C=
ENST00000686409.1:n.4314C= (RAF1)
ENST00000686455.1:n.3626C= (RAF1)
ENST00000686762.1:c.*31C= (RAF1)	ENSP00000509767.1:n.*31C=
ENST00000687257.1:n.3499C= (RAF1)
ENST00000687326.1:c.*2197C= (RAF1)	ENSP00000509665.1:n.*2197C=
ENST00000687505.1:n.1590C= (RAF1)
ENST00000687923.1:c.1361C= (RAF1)	ENSP00000510255.1:p.Thr454=
ENST00000688269.1:n.2068C= (RAF1)
ENST00000688444.1:n.3589C= (RAF1)
ENST00000688543.1:c.1373C= (RAF1)	ENSP00000509612.1:p.Thr458=
ENST00000688625.1:c.*2841C= (RAF1)	ENSP00000509522.1:n.*2841C=
ENST00000688803.1:n.2965-492C= (RAF1)
ENST00000688914.1:n.458C= (RAF1)
ENST00000689097.1:c.*1149C= (RAF1)	ENSP00000509756.1:n.*1149C=
ENST00000689389.1:c.1295C= (RAF1)	ENSP00000510213.1:p.Thr432=
ENST00000689418.1:c.*2940C= (RAF1)	ENSP00000509467.1:n.*2940C=
ENST00000689540.1:n.3413C= (RAF1)
ENST00000689876.1:c.1418-339C= (RAF1)	ENSP00000508535.1:n.1418-339C=
ENST00000689914.1:c.*406C= (RAF1)	ENSP00000509847.1:n.*406C=
ENST00000690397.1:c.1361C= (RAF1)	ENSP00000508730.1:p.Thr454=
ENST00000690460.1:c.1460C= (RAF1)	ENSP00000509106.1:p.Thr487=
ENST00000690585.1:c.263-492C= (RAF1)
ENST00000690625.1:n.2508C= (RAF1)
ENST00000691396.1:c.*1344C= (RAF1)	ENSP00000510712.1:n.*1344C=
ENST00000691643.1:n.2098C= (RAF1)
ENST00000691724.1:c.*429C= (RAF1)	ENSP00000509255.1:n.*429C=
ENST00000691779.1:c.*1050C= (RAF1)	ENSP00000508592.1:n.*1050C=
ENST00000691888.1:c.346C= (RAF1)
ENST00000691899.1:c.1472C= (RAF1)	ENSP00000508763.1:p.Thr491=
ENST00000692069.1:n.3829C= (RAF1)
ENST00000692093.1:c.1373C= (RAF1)	ENSP00000509669.1:p.Thr458=
ENST00000692311.1:n.2296C= (RAF1)
ENST00000692558.1:n.3628C= (RAF1)
ENST00000692773.1:c.*1209C= (RAF1)	ENSP00000509055.1:n.*1209C=
ENST00000692830.1:c.*1217C= (RAF1)	ENSP00000509461.1:n.*1217C=
ENST00000693312.1:c.1247C= (RAF1)	ENSP00000508686.1:p.Thr416=
ENST00000693664.1:c.1488-492C= (RAF1)	ENSP00000509614.1:n.1488-492C=
ENST00000693705.1:c.*1048-764C= (RAF1)	ENSP00000510697.1:n.*1048-764C=
ENST00000251849.9:c.1472C= (RAF1) MANE Select	ENSP00000251849.4:p.Thr491=
ENST00000442415.7:c.1532C= (RAF1)	ENSP00000401888.2:p.Thr511=
ENST00000676541.1:c.*3492G= (MKRN2)	ENSP00000503730.1:n.*3492G=
ENST00000677142.1:c.*3492G= (MKRN2)	ENSP00000504455.1:n.*3492G=
ENST00000677816.1:c.*2047G= (MKRN2)	ENSP00000502893.1:n.*2047G=
ENST00000677941.1:n.3555G= (MKRN2)
ENST00000251849.8:c.1472C= (RAF1)	ENSP00000251849.4:p.Thr491=
ENST00000423275.5:c.*1149C= (RAF1)	ENSP00000401088.1:n.*1149C=
ENST00000432427.2:c.1109C= (RAF1)	ENSP00000398591.2:p.Thr370=
ENST00000442415.6:c.1532C= (RAF1)	ENSP00000401888.2:p.Thr511=
ENST00000471449.1:n.161C= (RAF1)
NM_002880.3:c.1472C= , LRG_413t1:c.1472C= (RAF1)	NP_002871.1:p.Thr491=
XM_005265355.1:c.1472C= (RAF1)	XP_005265412.1:p.Thr491=
XM_005265357.1:c.1373C= (RAF1)	XP_005265414.1:p.Thr458=
XM_005265358.3:c.1229C= (RAF1)	XP_005265415.1:p.Thr410=
XM_005265359.3:c.1130C= (RAF1)	XP_005265416.1:p.Thr377=
XM_005265360.1:c.1418-339C= (RAF1)	XP_005265417.1:n.1418-339C=
XM_011533974.1:c.1472C= (RAF1)	XP_011532276.1:p.Thr491=
XM_011533975.1:c.1229C= (RAF1)	XP_011532277.1:p.Thr410=
NM_001354689.1:c.1532C= (RAF1)	NP_001341618.1:p.Thr511=
NM_001354690.1:c.1472C= (RAF1)	NP_001341619.1:p.Thr491=
NM_001354691.1:c.1229C= (RAF1)	NP_001341620.1:p.Thr410=
NM_001354692.1:c.1229C= (RAF1)	NP_001341621.1:p.Thr410=
NM_001354693.1:c.1373C= (RAF1)	NP_001341622.1:p.Thr458=
NM_001354694.1:c.1289C= (RAF1)	NP_001341623.1:p.Thr430=
NM_001354695.1:c.1130C= (RAF1)	NP_001341624.1:p.Thr377=
NR_148940.1:n.2000C= (RAF1)
NR_148941.1:n.1946C= (RAF1)
NR_148942.1:n.1885C= (RAF1)
XM_011533974.3:c.1472C= (RAF1)	XP_011532276.1:p.Thr491=
XM_017006966.1:c.1373C= (RAF1)	XP_016862455.1:p.Thr458=
NM_001354689.3:c.1532C= (RAF1)	NP_001341618.1:p.Thr511=
NM_001354690.2:c.1472C= (RAF1)	NP_001341619.1:p.Thr491=
NM_001354691.2:c.1229C= (RAF1)	NP_001341620.1:p.Thr410=
NM_001354692.2:c.1229C= (RAF1)	NP_001341621.1:p.Thr410=
NM_001354693.2:c.1373C= (RAF1)	NP_001341622.1:p.Thr458=
NM_001354694.2:c.1289C= (RAF1)	NP_001341623.1:p.Thr430=
NM_001354695.2:c.1130C= (RAF1)	NP_001341624.1:p.Thr377=
NR_148940.2:n.1916C= (RAF1)
NR_148941.2:n.1862C= (RAF1)
NR_148942.2:n.1801C= (RAF1)
NM_001354690.3:c.1472C= (RAF1)	NP_001341619.1:p.Thr491=
NM_001354691.3:c.1229C= (RAF1)	NP_001341620.1:p.Thr410=
NM_001354692.3:c.1229C= (RAF1)	NP_001341621.1:p.Thr410=
NM_001354693.3:c.1373C= (RAF1)	NP_001341622.1:p.Thr458=
NM_001354694.3:c.1289C= (RAF1)	NP_001341623.1:p.Thr430=
NM_001354695.3:c.1130C= (RAF1)	NP_001341624.1:p.Thr377=
NM_002880.4:c.1472C= (RAF1) MANE Select	NP_002871.1:p.Thr491=
NR_148940.3:n.1916C= (RAF1)
NR_148941.3:n.1862C= (RAF1)
NR_148942.3:n.1801C= (RAF1)