Canonical Allele Identifier: CA351496766

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626419C>T (hg19) ; chr3:g.12584920C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584920C>T , CM000665.2:g.12584920C>T	GRCh38
NC_000003.11:g.12626419C>T , CM000665.1:g.12626419C>T	GRCh37
NC_000003.10:g.12601419C>T	NCBI36
NG_007467.1:g.84260G>A , LRG_413:g.84260G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1395G>A (RAF1)	ENSP00000401088.1:n.*1395G>A
ENST00000432427.3:c.1047G>A (RAF1)
ENST00000460610.2:n.6042G>A (RAF1)
ENST00000471449.2:n.540G>A (RAF1)
ENST00000475353.2:n.4010G>A (RAF1)
ENST00000684903.1:c.*1407G>A (RAF1)	ENSP00000508612.1:n.*1407G>A
ENST00000685348.1:c.*1441G>A (RAF1)	ENSP00000510285.1:n.*1441G>A
ENST00000685437.1:c.1631G>A (RAF1)	ENSP00000508794.1:p.Cys544Tyr
ENST00000685653.1:c.1730G>A (RAF1)	ENSP00000509968.1:p.Cys577Tyr
ENST00000685697.1:n.2465G>A (RAF1)
ENST00000685738.1:c.*694G>A (RAF1)	ENSP00000510156.1:n.*694G>A
ENST00000686409.1:n.5139G>A (RAF1)
ENST00000686455.1:n.4451G>A (RAF1)
ENST00000686762.1:c.*289G>A (RAF1)	ENSP00000509767.1:n.*289G>A
ENST00000687257.1:n.4184G>A (RAF1)
ENST00000687326.1:c.*3022G>A (RAF1)	ENSP00000509665.1:n.*3022G>A
ENST00000687505.1:n.1848G>A (RAF1)
ENST00000687923.1:c.1619G>A (RAF1)	ENSP00000510255.1:p.Cys540Tyr
ENST00000688269.1:n.2326G>A (RAF1)
ENST00000688444.1:n.3847G>A (RAF1)
ENST00000688543.1:c.1631G>A (RAF1)	ENSP00000509612.1:p.Cys544Tyr
ENST00000688625.1:c.*3099G>A (RAF1)	ENSP00000509522.1:n.*3099G>A
ENST00000688803.1:n.3158G>A (RAF1)
ENST00000688914.1:n.1143G>A (RAF1)
ENST00000689097.1:c.*1407G>A (RAF1)	ENSP00000509756.1:n.*1407G>A
ENST00000689389.1:c.1553G>A (RAF1)	ENSP00000510213.1:p.Cys518Tyr
ENST00000689418.1:c.*3625G>A (RAF1)	ENSP00000509467.1:n.*3625G>A
ENST00000689540.1:n.4098G>A (RAF1)
ENST00000689876.1:c.*279G>A (RAF1)	ENSP00000508535.1:n.*279G>A
ENST00000689914.1:c.*664G>A (RAF1)	ENSP00000509847.1:n.*664G>A
ENST00000690397.1:c.1619G>A (RAF1)	ENSP00000508730.1:p.Cys540Tyr
ENST00000690460.1:c.1718G>A (RAF1)	ENSP00000509106.1:p.Cys573Tyr
ENST00000690585.1:c.456G>A (RAF1)
ENST00000690625.1:n.2766G>A (RAF1)
ENST00000691396.1:c.*1602G>A (RAF1)	ENSP00000510712.1:n.*1602G>A
ENST00000691643.1:n.2783G>A (RAF1)
ENST00000691724.1:c.*687G>A (RAF1)	ENSP00000509255.1:n.*687G>A
ENST00000691779.1:c.*1308G>A (RAF1)	ENSP00000508592.1:n.*1308G>A
ENST00000691888.1:c.604G>A (RAF1)
ENST00000691899.1:c.1730G>A (RAF1)	ENSP00000508763.1:p.Cys577Tyr
ENST00000692069.1:n.4654G>A (RAF1)
ENST00000692093.1:c.1631G>A (RAF1)	ENSP00000509669.1:p.Cys544Tyr
ENST00000692311.1:n.2554G>A (RAF1)
ENST00000692558.1:n.4313G>A (RAF1)
ENST00000692773.1:c.*1467G>A (RAF1)	ENSP00000509055.1:n.*1467G>A
ENST00000692830.1:c.*1475G>A (RAF1)	ENSP00000509461.1:n.*1475G>A
ENST00000693312.1:c.1505G>A (RAF1)	ENSP00000508686.1:p.Cys502Tyr
ENST00000693664.1:c.*181G>A (RAF1)	ENSP00000509614.1:n.*181G>A
ENST00000693705.1:c.*1109G>A (RAF1)	ENSP00000510697.1:n.*1109G>A
ENST00000251849.9:c.1730G>A (RAF1) MANE Select	ENSP00000251849.4:p.Cys577Tyr
ENST00000442415.7:c.1790G>A (RAF1)	ENSP00000401888.2:p.Cys597Tyr
ENST00000676541.1:c.*2667C>T (MKRN2)	ENSP00000503730.1:n.*2667C>T
ENST00000677142.1:c.*2667C>T (MKRN2)	ENSP00000504455.1:n.*2667C>T
ENST00000677816.1:c.*1222C>T (MKRN2)	ENSP00000502893.1:n.*1222C>T
ENST00000677941.1:n.2730C>T (MKRN2)
ENST00000251849.8:c.1730G>A (RAF1)	ENSP00000251849.4:p.Cys577Tyr
ENST00000423275.5:c.*1407G>A (RAF1)	ENSP00000401088.1:n.*1407G>A
ENST00000432427.2:c.1367G>A (RAF1)	ENSP00000398591.2:p.Cys456Tyr
ENST00000442415.6:c.1790G>A (RAF1)	ENSP00000401888.2:p.Cys597Tyr
ENST00000471449.1:n.419G>A (RAF1)
NM_002880.3:c.1730G>A , LRG_413t1:c.1730G>A (RAF1)	NP_002871.1:p.Cys577Tyr
XM_005265355.1:c.1730G>A (RAF1)	XP_005265412.1:p.Cys577Tyr
XM_005265357.1:c.1631G>A (RAF1)	XP_005265414.1:p.Cys544Tyr
XM_005265358.3:c.1487G>A (RAF1)	XP_005265415.1:p.Cys496Tyr
XM_005265359.3:c.1388G>A (RAF1)	XP_005265416.1:p.Cys463Tyr
XM_011533974.1:c.1730G>A (RAF1)	XP_011532276.1:p.Cys577Tyr
XM_011533975.1:c.1487G>A (RAF1)	XP_011532277.1:p.Cys496Tyr
NM_001354689.1:c.1790G>A (RAF1)	NP_001341618.1:p.Cys597Tyr
NM_001354690.1:c.1730G>A (RAF1)	NP_001341619.1:p.Cys577Tyr
NM_001354691.1:c.1487G>A (RAF1)	NP_001341620.1:p.Cys496Tyr
NM_001354692.1:c.1487G>A (RAF1)	NP_001341621.1:p.Cys496Tyr
NM_001354693.1:c.1631G>A (RAF1)	NP_001341622.1:p.Cys544Tyr
NM_001354694.1:c.1547G>A (RAF1)	NP_001341623.1:p.Cys516Tyr
NM_001354695.1:c.1388G>A (RAF1)	NP_001341624.1:p.Cys463Tyr
NR_148940.1:n.2258G>A (RAF1)
NR_148941.1:n.2204G>A (RAF1)
NR_148942.1:n.2143G>A (RAF1)
XM_011533974.3:c.1730G>A (RAF1)	XP_011532276.1:p.Cys577Tyr
XM_017006966.1:c.1631G>A (RAF1)	XP_016862455.1:p.Cys544Tyr
NM_001354689.3:c.1790G>A (RAF1)	NP_001341618.1:p.Cys597Tyr
NM_001354690.2:c.1730G>A (RAF1)	NP_001341619.1:p.Cys577Tyr
NM_001354691.2:c.1487G>A (RAF1)	NP_001341620.1:p.Cys496Tyr
NM_001354692.2:c.1487G>A (RAF1)	NP_001341621.1:p.Cys496Tyr
NM_001354693.2:c.1631G>A (RAF1)	NP_001341622.1:p.Cys544Tyr
NM_001354694.2:c.1547G>A (RAF1)	NP_001341623.1:p.Cys516Tyr
NM_001354695.2:c.1388G>A (RAF1)	NP_001341624.1:p.Cys463Tyr
NR_148940.2:n.2174G>A (RAF1)
NR_148941.2:n.2120G>A (RAF1)
NR_148942.2:n.2059G>A (RAF1)
NM_001354690.3:c.1730G>A (RAF1)	NP_001341619.1:p.Cys577Tyr
NM_001354691.3:c.1487G>A (RAF1)	NP_001341620.1:p.Cys496Tyr
NM_001354692.3:c.1487G>A (RAF1)	NP_001341621.1:p.Cys496Tyr
NM_001354693.3:c.1631G>A (RAF1)	NP_001341622.1:p.Cys544Tyr
NM_001354694.3:c.1547G>A (RAF1)	NP_001341623.1:p.Cys516Tyr
NM_001354695.3:c.1388G>A (RAF1)	NP_001341624.1:p.Cys463Tyr
NM_002880.4:c.1730G>A (RAF1) MANE Select	NP_002871.1:p.Cys577Tyr
NR_148940.3:n.2174G>A (RAF1)
NR_148941.3:n.2120G>A (RAF1)
NR_148942.3:n.2059G>A (RAF1)