Canonical Allele Identifier: CA351496771

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626420A>T (hg19) ; chr3:g.12584921A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584921A>T , CM000665.2:g.12584921A>T	GRCh38
NC_000003.11:g.12626420A>T , CM000665.1:g.12626420A>T	GRCh37
NC_000003.10:g.12601420A>T	NCBI36
NG_007467.1:g.84259T>A , LRG_413:g.84259T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1394T>A (RAF1)	ENSP00000401088.1:n.*1394T>A
ENST00000432427.3:c.1046T>A (RAF1)
ENST00000460610.2:n.6041T>A (RAF1)
ENST00000471449.2:n.539T>A (RAF1)
ENST00000475353.2:n.4009T>A (RAF1)
ENST00000684903.1:c.*1406T>A (RAF1)	ENSP00000508612.1:n.*1406T>A
ENST00000685348.1:c.*1440T>A (RAF1)	ENSP00000510285.1:n.*1440T>A
ENST00000685437.1:c.1630T>A (RAF1)	ENSP00000508794.1:p.Cys544Ser
ENST00000685653.1:c.1729T>A (RAF1)	ENSP00000509968.1:p.Cys577Ser
ENST00000685697.1:n.2464T>A (RAF1)
ENST00000685738.1:c.*693T>A (RAF1)	ENSP00000510156.1:n.*693T>A
ENST00000686409.1:n.5138T>A (RAF1)
ENST00000686455.1:n.4450T>A (RAF1)
ENST00000686762.1:c.*288T>A (RAF1)	ENSP00000509767.1:n.*288T>A
ENST00000687257.1:n.4183T>A (RAF1)
ENST00000687326.1:c.*3021T>A (RAF1)	ENSP00000509665.1:n.*3021T>A
ENST00000687505.1:n.1847T>A (RAF1)
ENST00000687923.1:c.1618T>A (RAF1)	ENSP00000510255.1:p.Cys540Ser
ENST00000688269.1:n.2325T>A (RAF1)
ENST00000688444.1:n.3846T>A (RAF1)
ENST00000688543.1:c.1630T>A (RAF1)	ENSP00000509612.1:p.Cys544Ser
ENST00000688625.1:c.*3098T>A (RAF1)	ENSP00000509522.1:n.*3098T>A
ENST00000688803.1:n.3157T>A (RAF1)
ENST00000688914.1:n.1142T>A (RAF1)
ENST00000689097.1:c.*1406T>A (RAF1)	ENSP00000509756.1:n.*1406T>A
ENST00000689389.1:c.1552T>A (RAF1)	ENSP00000510213.1:p.Cys518Ser
ENST00000689418.1:c.*3624T>A (RAF1)	ENSP00000509467.1:n.*3624T>A
ENST00000689540.1:n.4097T>A (RAF1)
ENST00000689876.1:c.*278T>A (RAF1)	ENSP00000508535.1:n.*278T>A
ENST00000689914.1:c.*663T>A (RAF1)	ENSP00000509847.1:n.*663T>A
ENST00000690397.1:c.1618T>A (RAF1)	ENSP00000508730.1:p.Cys540Ser
ENST00000690460.1:c.1717T>A (RAF1)	ENSP00000509106.1:p.Cys573Ser
ENST00000690585.1:c.455T>A (RAF1)
ENST00000690625.1:n.2765T>A (RAF1)
ENST00000691396.1:c.*1601T>A (RAF1)	ENSP00000510712.1:n.*1601T>A
ENST00000691643.1:n.2782T>A (RAF1)
ENST00000691724.1:c.*686T>A (RAF1)	ENSP00000509255.1:n.*686T>A
ENST00000691779.1:c.*1307T>A (RAF1)	ENSP00000508592.1:n.*1307T>A
ENST00000691888.1:c.603T>A (RAF1)
ENST00000691899.1:c.1729T>A (RAF1)	ENSP00000508763.1:p.Cys577Ser
ENST00000692069.1:n.4653T>A (RAF1)
ENST00000692093.1:c.1630T>A (RAF1)	ENSP00000509669.1:p.Cys544Ser
ENST00000692311.1:n.2553T>A (RAF1)
ENST00000692558.1:n.4312T>A (RAF1)
ENST00000692773.1:c.*1466T>A (RAF1)	ENSP00000509055.1:n.*1466T>A
ENST00000692830.1:c.*1474T>A (RAF1)	ENSP00000509461.1:n.*1474T>A
ENST00000693312.1:c.1504T>A (RAF1)	ENSP00000508686.1:p.Cys502Ser
ENST00000693664.1:c.*180T>A (RAF1)	ENSP00000509614.1:n.*180T>A
ENST00000693705.1:c.*1108T>A (RAF1)	ENSP00000510697.1:n.*1108T>A
ENST00000251849.9:c.1729T>A (RAF1) MANE Select	ENSP00000251849.4:p.Cys577Ser
ENST00000442415.7:c.1789T>A (RAF1)	ENSP00000401888.2:p.Cys597Ser
ENST00000676541.1:c.*2668A>T (MKRN2)	ENSP00000503730.1:n.*2668A>T
ENST00000677142.1:c.*2668A>T (MKRN2)	ENSP00000504455.1:n.*2668A>T
ENST00000677816.1:c.*1223A>T (MKRN2)	ENSP00000502893.1:n.*1223A>T
ENST00000677941.1:n.2731A>T (MKRN2)
ENST00000251849.8:c.1729T>A (RAF1)	ENSP00000251849.4:p.Cys577Ser
ENST00000423275.5:c.*1406T>A (RAF1)	ENSP00000401088.1:n.*1406T>A
ENST00000432427.2:c.1366T>A (RAF1)	ENSP00000398591.2:p.Cys456Ser
ENST00000442415.6:c.1789T>A (RAF1)	ENSP00000401888.2:p.Cys597Ser
ENST00000471449.1:n.418T>A (RAF1)
NM_002880.3:c.1729T>A , LRG_413t1:c.1729T>A (RAF1)	NP_002871.1:p.Cys577Ser
XM_005265355.1:c.1729T>A (RAF1)	XP_005265412.1:p.Cys577Ser
XM_005265357.1:c.1630T>A (RAF1)	XP_005265414.1:p.Cys544Ser
XM_005265358.3:c.1486T>A (RAF1)	XP_005265415.1:p.Cys496Ser
XM_005265359.3:c.1387T>A (RAF1)	XP_005265416.1:p.Cys463Ser
XM_011533974.1:c.1729T>A (RAF1)	XP_011532276.1:p.Cys577Ser
XM_011533975.1:c.1486T>A (RAF1)	XP_011532277.1:p.Cys496Ser
NM_001354689.1:c.1789T>A (RAF1)	NP_001341618.1:p.Cys597Ser
NM_001354690.1:c.1729T>A (RAF1)	NP_001341619.1:p.Cys577Ser
NM_001354691.1:c.1486T>A (RAF1)	NP_001341620.1:p.Cys496Ser
NM_001354692.1:c.1486T>A (RAF1)	NP_001341621.1:p.Cys496Ser
NM_001354693.1:c.1630T>A (RAF1)	NP_001341622.1:p.Cys544Ser
NM_001354694.1:c.1546T>A (RAF1)	NP_001341623.1:p.Cys516Ser
NM_001354695.1:c.1387T>A (RAF1)	NP_001341624.1:p.Cys463Ser
NR_148940.1:n.2257T>A (RAF1)
NR_148941.1:n.2203T>A (RAF1)
NR_148942.1:n.2142T>A (RAF1)
XM_011533974.3:c.1729T>A (RAF1)	XP_011532276.1:p.Cys577Ser
XM_017006966.1:c.1630T>A (RAF1)	XP_016862455.1:p.Cys544Ser
NM_001354689.3:c.1789T>A (RAF1)	NP_001341618.1:p.Cys597Ser
NM_001354690.2:c.1729T>A (RAF1)	NP_001341619.1:p.Cys577Ser
NM_001354691.2:c.1486T>A (RAF1)	NP_001341620.1:p.Cys496Ser
NM_001354692.2:c.1486T>A (RAF1)	NP_001341621.1:p.Cys496Ser
NM_001354693.2:c.1630T>A (RAF1)	NP_001341622.1:p.Cys544Ser
NM_001354694.2:c.1546T>A (RAF1)	NP_001341623.1:p.Cys516Ser
NM_001354695.2:c.1387T>A (RAF1)	NP_001341624.1:p.Cys463Ser
NR_148940.2:n.2173T>A (RAF1)
NR_148941.2:n.2119T>A (RAF1)
NR_148942.2:n.2058T>A (RAF1)
NM_001354690.3:c.1729T>A (RAF1)	NP_001341619.1:p.Cys577Ser
NM_001354691.3:c.1486T>A (RAF1)	NP_001341620.1:p.Cys496Ser
NM_001354692.3:c.1486T>A (RAF1)	NP_001341621.1:p.Cys496Ser
NM_001354693.3:c.1630T>A (RAF1)	NP_001341622.1:p.Cys544Ser
NM_001354694.3:c.1546T>A (RAF1)	NP_001341623.1:p.Cys516Ser
NM_001354695.3:c.1387T>A (RAF1)	NP_001341624.1:p.Cys463Ser
NM_002880.4:c.1729T>A (RAF1) MANE Select	NP_002871.1:p.Cys577Ser
NR_148940.3:n.2173T>A (RAF1)
NR_148941.3:n.2119T>A (RAF1)
NR_148942.3:n.2058T>A (RAF1)