Canonical Allele Identifier: CA351499147

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12627257A>C (hg19) ; chr3:g.12585758A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585758A>C , CM000665.2:g.12585758A>C	GRCh38
NC_000003.11:g.12627257A>C , CM000665.1:g.12627257A>C	GRCh37
NC_000003.10:g.12602257A>C	NCBI36
NG_007467.1:g.83422T>G , LRG_413:g.83422T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1124T>G (RAF1)	ENSP00000401088.1:n.*1124T>G
ENST00000432427.3:c.776T>G (RAF1)
ENST00000460610.2:n.5204T>G (RAF1)
ENST00000471449.2:n.269T>G (RAF1)
ENST00000475353.2:n.3172T>G (RAF1)
ENST00000684903.1:c.*1136T>G (RAF1)	ENSP00000508612.1:n.*1136T>G
ENST00000685348.1:c.*1095-352T>G (RAF1)	ENSP00000510285.1:n.*1095-352T>G
ENST00000685437.1:c.1360T>G (RAF1)	ENSP00000508794.1:p.Phe454Val
ENST00000685653.1:c.1459T>G (RAF1)	ENSP00000509968.1:p.Phe487Val
ENST00000685697.1:n.2194T>G (RAF1)
ENST00000685738.1:c.*423T>G (RAF1)	ENSP00000510156.1:n.*423T>G
ENST00000686409.1:n.4301T>G (RAF1)
ENST00000686455.1:n.3613T>G (RAF1)
ENST00000686762.1:c.*18T>G (RAF1)	ENSP00000509767.1:n.*18T>G
ENST00000687257.1:n.3486T>G (RAF1)
ENST00000687326.1:c.*2184T>G (RAF1)	ENSP00000509665.1:n.*2184T>G
ENST00000687505.1:n.1577T>G (RAF1)
ENST00000687923.1:c.1348T>G (RAF1)	ENSP00000510255.1:p.Phe450Val
ENST00000688269.1:n.2055T>G (RAF1)
ENST00000688444.1:n.3576T>G (RAF1)
ENST00000688543.1:c.1360T>G (RAF1)	ENSP00000509612.1:p.Phe454Val
ENST00000688625.1:c.*2828T>G (RAF1)	ENSP00000509522.1:n.*2828T>G
ENST00000688803.1:n.2965-505T>G (RAF1)
ENST00000688914.1:n.445T>G (RAF1)
ENST00000689097.1:c.*1136T>G (RAF1)	ENSP00000509756.1:n.*1136T>G
ENST00000689389.1:c.1282T>G (RAF1)	ENSP00000510213.1:p.Phe428Val
ENST00000689418.1:c.*2927T>G (RAF1)	ENSP00000509467.1:n.*2927T>G
ENST00000689540.1:n.3400T>G (RAF1)
ENST00000689876.1:c.1418-352T>G (RAF1)	ENSP00000508535.1:n.1418-352T>G
ENST00000689914.1:c.*393T>G (RAF1)	ENSP00000509847.1:n.*393T>G
ENST00000690397.1:c.1348T>G (RAF1)	ENSP00000508730.1:p.Phe450Val
ENST00000690460.1:c.1447T>G (RAF1)	ENSP00000509106.1:p.Phe483Val
ENST00000690585.1:c.263-505T>G (RAF1)
ENST00000690625.1:n.2495T>G (RAF1)
ENST00000691396.1:c.*1331T>G (RAF1)	ENSP00000510712.1:n.*1331T>G
ENST00000691643.1:n.2085T>G (RAF1)
ENST00000691724.1:c.*416T>G (RAF1)	ENSP00000509255.1:n.*416T>G
ENST00000691779.1:c.*1037T>G (RAF1)	ENSP00000508592.1:n.*1037T>G
ENST00000691888.1:c.333T>G (RAF1)
ENST00000691899.1:c.1459T>G (RAF1)	ENSP00000508763.1:p.Phe487Val
ENST00000692069.1:n.3816T>G (RAF1)
ENST00000692093.1:c.1360T>G (RAF1)	ENSP00000509669.1:p.Phe454Val
ENST00000692311.1:n.2283T>G (RAF1)
ENST00000692558.1:n.3615T>G (RAF1)
ENST00000692773.1:c.*1196T>G (RAF1)	ENSP00000509055.1:n.*1196T>G
ENST00000692830.1:c.*1204T>G (RAF1)	ENSP00000509461.1:n.*1204T>G
ENST00000693312.1:c.1234T>G (RAF1)	ENSP00000508686.1:p.Phe412Val
ENST00000693664.1:c.1488-505T>G (RAF1)	ENSP00000509614.1:n.1488-505T>G
ENST00000693705.1:c.*1048-777T>G (RAF1)	ENSP00000510697.1:n.*1048-777T>G
ENST00000251849.9:c.1459T>G (RAF1) MANE Select	ENSP00000251849.4:p.Phe487Val
ENST00000442415.7:c.1519T>G (RAF1)	ENSP00000401888.2:p.Phe507Val
ENST00000676541.1:c.*3505A>C (MKRN2)	ENSP00000503730.1:n.*3505A>C
ENST00000677142.1:c.*3505A>C (MKRN2)	ENSP00000504455.1:n.*3505A>C
ENST00000677816.1:c.*2060A>C (MKRN2)	ENSP00000502893.1:n.*2060A>C
ENST00000677941.1:n.3568A>C (MKRN2)
ENST00000251849.8:c.1459T>G (RAF1)	ENSP00000251849.4:p.Phe487Val
ENST00000423275.5:c.*1136T>G (RAF1)	ENSP00000401088.1:n.*1136T>G
ENST00000432427.2:c.1096T>G (RAF1)	ENSP00000398591.2:p.Phe366Val
ENST00000442415.6:c.1519T>G (RAF1)	ENSP00000401888.2:p.Phe507Val
ENST00000471449.1:n.148T>G (RAF1)
NM_002880.3:c.1459T>G , LRG_413t1:c.1459T>G (RAF1)	NP_002871.1:p.Phe487Val
XM_005265355.1:c.1459T>G (RAF1)	XP_005265412.1:p.Phe487Val
XM_005265357.1:c.1360T>G (RAF1)	XP_005265414.1:p.Phe454Val
XM_005265358.3:c.1216T>G (RAF1)	XP_005265415.1:p.Phe406Val
XM_005265359.3:c.1117T>G (RAF1)	XP_005265416.1:p.Phe373Val
XM_005265360.1:c.1418-352T>G (RAF1)	XP_005265417.1:n.1418-352T>G
XM_011533974.1:c.1459T>G (RAF1)	XP_011532276.1:p.Phe487Val
XM_011533975.1:c.1216T>G (RAF1)	XP_011532277.1:p.Phe406Val
NM_001354689.1:c.1519T>G (RAF1)	NP_001341618.1:p.Phe507Val
NM_001354690.1:c.1459T>G (RAF1)	NP_001341619.1:p.Phe487Val
NM_001354691.1:c.1216T>G (RAF1)	NP_001341620.1:p.Phe406Val
NM_001354692.1:c.1216T>G (RAF1)	NP_001341621.1:p.Phe406Val
NM_001354693.1:c.1360T>G (RAF1)	NP_001341622.1:p.Phe454Val
NM_001354694.1:c.1276T>G (RAF1)	NP_001341623.1:p.Phe426Val
NM_001354695.1:c.1117T>G (RAF1)	NP_001341624.1:p.Phe373Val
NR_148940.1:n.1987T>G (RAF1)
NR_148941.1:n.1933T>G (RAF1)
NR_148942.1:n.1872T>G (RAF1)
XM_011533974.3:c.1459T>G (RAF1)	XP_011532276.1:p.Phe487Val
XM_017006966.1:c.1360T>G (RAF1)	XP_016862455.1:p.Phe454Val
NM_001354689.3:c.1519T>G (RAF1)	NP_001341618.1:p.Phe507Val
NM_001354690.2:c.1459T>G (RAF1)	NP_001341619.1:p.Phe487Val
NM_001354691.2:c.1216T>G (RAF1)	NP_001341620.1:p.Phe406Val
NM_001354692.2:c.1216T>G (RAF1)	NP_001341621.1:p.Phe406Val
NM_001354693.2:c.1360T>G (RAF1)	NP_001341622.1:p.Phe454Val
NM_001354694.2:c.1276T>G (RAF1)	NP_001341623.1:p.Phe426Val
NM_001354695.2:c.1117T>G (RAF1)	NP_001341624.1:p.Phe373Val
NR_148940.2:n.1903T>G (RAF1)
NR_148941.2:n.1849T>G (RAF1)
NR_148942.2:n.1788T>G (RAF1)
NM_001354690.3:c.1459T>G (RAF1)	NP_001341619.1:p.Phe487Val
NM_001354691.3:c.1216T>G (RAF1)	NP_001341620.1:p.Phe406Val
NM_001354692.3:c.1216T>G (RAF1)	NP_001341621.1:p.Phe406Val
NM_001354693.3:c.1360T>G (RAF1)	NP_001341622.1:p.Phe454Val
NM_001354694.3:c.1276T>G (RAF1)	NP_001341623.1:p.Phe426Val
NM_001354695.3:c.1117T>G (RAF1)	NP_001341624.1:p.Phe373Val
NM_002880.4:c.1459T>G (RAF1) MANE Select	NP_002871.1:p.Phe487Val
NR_148940.3:n.1903T>G (RAF1)
NR_148941.3:n.1849T>G (RAF1)
NR_148942.3:n.1788T>G (RAF1)