Canonical Allele Identifier: CA432272840

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs2125326034
• MyVariant Identifiers: chr3:g.12627234T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585735T>A , CM000665.2:g.12585735T>A	GRCh38
NC_000003.11:g.12627234T>A , CM000665.1:g.12627234T>A	GRCh37
NC_000003.10:g.12602234T>A	NCBI36
NG_007467.1:g.83445A>T , LRG_413:g.83445A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1147A>T (RAF1)	ENSP00000401088.1:n.*1147A>T
ENST00000432427.3:c.799A>T (RAF1)
ENST00000460610.2:n.5227A>T (RAF1)
ENST00000471449.2:n.292A>T (RAF1)
ENST00000475353.2:n.3195A>T (RAF1)
ENST00000684903.1:c.*1159A>T (RAF1)	ENSP00000508612.1:n.*1159A>T
ENST00000685348.1:c.*1095-329A>T (RAF1)	ENSP00000510285.1:n.*1095-329A>T
ENST00000685437.1:c.1383A>T (RAF1)	ENSP00000508794.1:p.Ser461=
ENST00000685653.1:c.1482A>T (RAF1)	ENSP00000509968.1:p.Ser494=
ENST00000685697.1:n.2217A>T (RAF1)
ENST00000685738.1:c.*446A>T (RAF1)	ENSP00000510156.1:n.*446A>T
ENST00000686409.1:n.4324A>T (RAF1)
ENST00000686455.1:n.3636A>T (RAF1)
ENST00000686762.1:c.*41A>T (RAF1)	ENSP00000509767.1:n.*41A>T
ENST00000687257.1:n.3509A>T (RAF1)
ENST00000687326.1:c.*2207A>T (RAF1)	ENSP00000509665.1:n.*2207A>T
ENST00000687505.1:n.1600A>T (RAF1)
ENST00000687923.1:c.1371A>T (RAF1)	ENSP00000510255.1:p.Ser457=
ENST00000688269.1:n.2078A>T (RAF1)
ENST00000688444.1:n.3599A>T (RAF1)
ENST00000688543.1:c.1383A>T (RAF1)	ENSP00000509612.1:p.Ser461=
ENST00000688625.1:c.*2851A>T (RAF1)	ENSP00000509522.1:n.*2851A>T
ENST00000688803.1:n.2965-482A>T (RAF1)
ENST00000688914.1:n.468A>T (RAF1)
ENST00000689097.1:c.*1159A>T (RAF1)	ENSP00000509756.1:n.*1159A>T
ENST00000689389.1:c.1305A>T (RAF1)	ENSP00000510213.1:p.Ser435=
ENST00000689418.1:c.*2950A>T (RAF1)	ENSP00000509467.1:n.*2950A>T
ENST00000689540.1:n.3423A>T (RAF1)
ENST00000689876.1:c.1418-329A>T (RAF1)	ENSP00000508535.1:n.1418-329A>T
ENST00000689914.1:c.*416A>T (RAF1)	ENSP00000509847.1:n.*416A>T
ENST00000690397.1:c.1371A>T (RAF1)	ENSP00000508730.1:p.Ser457=
ENST00000690460.1:c.1470A>T (RAF1)	ENSP00000509106.1:p.Ser490=
ENST00000690585.1:c.263-482A>T (RAF1)
ENST00000690625.1:n.2518A>T (RAF1)
ENST00000691396.1:c.*1354A>T (RAF1)	ENSP00000510712.1:n.*1354A>T
ENST00000691643.1:n.2108A>T (RAF1)
ENST00000691724.1:c.*439A>T (RAF1)	ENSP00000509255.1:n.*439A>T
ENST00000691779.1:c.*1060A>T (RAF1)	ENSP00000508592.1:n.*1060A>T
ENST00000691888.1:c.356A>T (RAF1)
ENST00000691899.1:c.1482A>T (RAF1)	ENSP00000508763.1:p.Ser494=
ENST00000692069.1:n.3839A>T (RAF1)
ENST00000692093.1:c.1383A>T (RAF1)	ENSP00000509669.1:p.Ser461=
ENST00000692311.1:n.2306A>T (RAF1)
ENST00000692558.1:n.3638A>T (RAF1)
ENST00000692773.1:c.*1219A>T (RAF1)	ENSP00000509055.1:n.*1219A>T
ENST00000692830.1:c.*1227A>T (RAF1)	ENSP00000509461.1:n.*1227A>T
ENST00000693312.1:c.1257A>T (RAF1)	ENSP00000508686.1:p.Ser419=
ENST00000693664.1:c.1488-482A>T (RAF1)	ENSP00000509614.1:n.1488-482A>T
ENST00000693705.1:c.*1048-754A>T (RAF1)	ENSP00000510697.1:n.*1048-754A>T
ENST00000251849.9:c.1482A>T (RAF1) MANE Select	ENSP00000251849.4:p.Ser494=
ENST00000442415.7:c.1542A>T (RAF1)	ENSP00000401888.2:p.Ser514=
ENST00000676541.1:c.*3482T>A (MKRN2)	ENSP00000503730.1:n.*3482T>A
ENST00000677142.1:c.*3482T>A (MKRN2)	ENSP00000504455.1:n.*3482T>A
ENST00000677816.1:c.*2037T>A (MKRN2)	ENSP00000502893.1:n.*2037T>A
ENST00000677941.1:n.3545T>A (MKRN2)
ENST00000251849.8:c.1482A>T (RAF1)	ENSP00000251849.4:p.Ser494=
ENST00000423275.5:c.*1159A>T (RAF1)	ENSP00000401088.1:n.*1159A>T
ENST00000432427.2:c.1119A>T (RAF1)	ENSP00000398591.2:p.Ser373=
ENST00000442415.6:c.1542A>T (RAF1)	ENSP00000401888.2:p.Ser514=
ENST00000471449.1:n.171A>T (RAF1)
NM_002880.3:c.1482A>T , LRG_413t1:c.1482A>T (RAF1)	NP_002871.1:p.Ser494=
XM_005265355.1:c.1482A>T (RAF1)	XP_005265412.1:p.Ser494=
XM_005265357.1:c.1383A>T (RAF1)	XP_005265414.1:p.Ser461=
XM_005265358.3:c.1239A>T (RAF1)	XP_005265415.1:p.Ser413=
XM_005265359.3:c.1140A>T (RAF1)	XP_005265416.1:p.Ser380=
XM_005265360.1:c.1418-329A>T (RAF1)	XP_005265417.1:n.1418-329A>T
XM_011533974.1:c.1482A>T (RAF1)	XP_011532276.1:p.Ser494=
XM_011533975.1:c.1239A>T (RAF1)	XP_011532277.1:p.Ser413=
NM_001354689.1:c.1542A>T (RAF1)	NP_001341618.1:p.Ser514=
NM_001354690.1:c.1482A>T (RAF1)	NP_001341619.1:p.Ser494=
NM_001354691.1:c.1239A>T (RAF1)	NP_001341620.1:p.Ser413=
NM_001354692.1:c.1239A>T (RAF1)	NP_001341621.1:p.Ser413=
NM_001354693.1:c.1383A>T (RAF1)	NP_001341622.1:p.Ser461=
NM_001354694.1:c.1299A>T (RAF1)	NP_001341623.1:p.Ser433=
NM_001354695.1:c.1140A>T (RAF1)	NP_001341624.1:p.Ser380=
NR_148940.1:n.2010A>T (RAF1)
NR_148941.1:n.1956A>T (RAF1)
NR_148942.1:n.1895A>T (RAF1)
XM_011533974.3:c.1482A>T (RAF1)	XP_011532276.1:p.Ser494=
XM_017006966.1:c.1383A>T (RAF1)	XP_016862455.1:p.Ser461=
NM_001354689.3:c.1542A>T (RAF1)	NP_001341618.1:p.Ser514=
NM_001354690.2:c.1482A>T (RAF1)	NP_001341619.1:p.Ser494=
NM_001354691.2:c.1239A>T (RAF1)	NP_001341620.1:p.Ser413=
NM_001354692.2:c.1239A>T (RAF1)	NP_001341621.1:p.Ser413=
NM_001354693.2:c.1383A>T (RAF1)	NP_001341622.1:p.Ser461=
NM_001354694.2:c.1299A>T (RAF1)	NP_001341623.1:p.Ser433=
NM_001354695.2:c.1140A>T (RAF1)	NP_001341624.1:p.Ser380=
NR_148940.2:n.1926A>T (RAF1)
NR_148941.2:n.1872A>T (RAF1)
NR_148942.2:n.1811A>T (RAF1)
NM_001354690.3:c.1482A>T (RAF1)	NP_001341619.1:p.Ser494=
NM_001354691.3:c.1239A>T (RAF1)	NP_001341620.1:p.Ser413=
NM_001354692.3:c.1239A>T (RAF1)	NP_001341621.1:p.Ser413=
NM_001354693.3:c.1383A>T (RAF1)	NP_001341622.1:p.Ser461=
NM_001354694.3:c.1299A>T (RAF1)	NP_001341623.1:p.Ser433=
NM_001354695.3:c.1140A>T (RAF1)	NP_001341624.1:p.Ser380=
NM_002880.4:c.1482A>T (RAF1) MANE Select	NP_002871.1:p.Ser494=
NR_148940.3:n.1926A>T (RAF1)
NR_148941.3:n.1872A>T (RAF1)
NR_148942.3:n.1811A>T (RAF1)