Canonical Allele Identifier: CA351496623

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626386C>T (hg19) ; chr3:g.12584887C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584887C>T , CM000665.2:g.12584887C>T	GRCh38
NC_000003.11:g.12626386C>T , CM000665.1:g.12626386C>T	GRCh37
NC_000003.10:g.12601386C>T	NCBI36
NG_007467.1:g.84293G>A , LRG_413:g.84293G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1428G>A (RAF1)	ENSP00000401088.1:n.*1428G>A
ENST00000432427.3:c.1080G>A (RAF1)
ENST00000460610.2:n.6075G>A (RAF1)
ENST00000471449.2:n.573G>A (RAF1)
ENST00000475353.2:n.4043G>A (RAF1)
ENST00000684903.1:c.*1440G>A (RAF1)	ENSP00000508612.1:n.*1440G>A
ENST00000685348.1:c.*1474G>A (RAF1)	ENSP00000510285.1:n.*1474G>A
ENST00000685437.1:c.1664G>A (RAF1)	ENSP00000508794.1:p.Cys555Tyr
ENST00000685653.1:c.1763G>A (RAF1)	ENSP00000509968.1:p.Cys588Tyr
ENST00000685697.1:n.2498G>A (RAF1)
ENST00000685738.1:c.*727G>A (RAF1)	ENSP00000510156.1:n.*727G>A
ENST00000686409.1:n.5172G>A (RAF1)
ENST00000686455.1:n.4484G>A (RAF1)
ENST00000686762.1:c.*322G>A (RAF1)	ENSP00000509767.1:n.*322G>A
ENST00000687257.1:n.4217G>A (RAF1)
ENST00000687326.1:c.*3055G>A (RAF1)	ENSP00000509665.1:n.*3055G>A
ENST00000687505.1:n.1881G>A (RAF1)
ENST00000687923.1:c.1652G>A (RAF1)	ENSP00000510255.1:p.Cys551Tyr
ENST00000688269.1:n.2359G>A (RAF1)
ENST00000688444.1:n.3880G>A (RAF1)
ENST00000688543.1:c.1664G>A (RAF1)	ENSP00000509612.1:p.Cys555Tyr
ENST00000688625.1:c.*3132G>A (RAF1)	ENSP00000509522.1:n.*3132G>A
ENST00000688803.1:n.3191G>A (RAF1)
ENST00000689097.1:c.*1440G>A (RAF1)	ENSP00000509756.1:n.*1440G>A
ENST00000689389.1:c.1586G>A (RAF1)	ENSP00000510213.1:p.Cys529Tyr
ENST00000689418.1:c.*3658G>A (RAF1)	ENSP00000509467.1:n.*3658G>A
ENST00000689540.1:n.4131G>A (RAF1)
ENST00000689876.1:c.*312G>A (RAF1)	ENSP00000508535.1:n.*312G>A
ENST00000689914.1:c.*697G>A (RAF1)	ENSP00000509847.1:n.*697G>A
ENST00000690397.1:c.1652G>A (RAF1)	ENSP00000508730.1:p.Cys551Tyr
ENST00000690460.1:c.1751G>A (RAF1)	ENSP00000509106.1:p.Cys584Tyr
ENST00000690585.1:c.489G>A (RAF1)
ENST00000690625.1:n.2799G>A (RAF1)
ENST00000691396.1:c.*1635G>A (RAF1)	ENSP00000510712.1:n.*1635G>A
ENST00000691643.1:n.2816G>A (RAF1)
ENST00000691724.1:c.*720G>A (RAF1)	ENSP00000509255.1:n.*720G>A
ENST00000691779.1:c.*1341G>A (RAF1)	ENSP00000508592.1:n.*1341G>A
ENST00000691888.1:c.637G>A (RAF1)
ENST00000691899.1:c.1763G>A (RAF1)	ENSP00000508763.1:p.Cys588Tyr
ENST00000692069.1:n.4687G>A (RAF1)
ENST00000692093.1:c.1664G>A (RAF1)	ENSP00000509669.1:p.Cys555Tyr
ENST00000692311.1:n.2587G>A (RAF1)
ENST00000692558.1:n.4346G>A (RAF1)
ENST00000692773.1:c.*1500G>A (RAF1)	ENSP00000509055.1:n.*1500G>A
ENST00000692830.1:c.*1508G>A (RAF1)	ENSP00000509461.1:n.*1508G>A
ENST00000693312.1:c.1538G>A (RAF1)	ENSP00000508686.1:p.Cys513Tyr
ENST00000693664.1:c.*214G>A (RAF1)	ENSP00000509614.1:n.*214G>A
ENST00000693705.1:c.*1142G>A (RAF1)	ENSP00000510697.1:n.*1142G>A
ENST00000251849.9:c.1763G>A (RAF1) MANE Select	ENSP00000251849.4:p.Cys588Tyr
ENST00000442415.7:c.1823G>A (RAF1)	ENSP00000401888.2:p.Cys608Tyr
ENST00000676541.1:c.*2634C>T (MKRN2)	ENSP00000503730.1:n.*2634C>T
ENST00000677142.1:c.*2634C>T (MKRN2)	ENSP00000504455.1:n.*2634C>T
ENST00000677816.1:c.*1189C>T (MKRN2)	ENSP00000502893.1:n.*1189C>T
ENST00000677941.1:n.2697C>T (MKRN2)
ENST00000251849.8:c.1763G>A (RAF1)	ENSP00000251849.4:p.Cys588Tyr
ENST00000423275.5:c.*1440G>A (RAF1)	ENSP00000401088.1:n.*1440G>A
ENST00000432427.2:c.1400G>A (RAF1)	ENSP00000398591.2:p.Cys467Tyr
ENST00000442415.6:c.1823G>A (RAF1)	ENSP00000401888.2:p.Cys608Tyr
ENST00000471449.1:n.452G>A (RAF1)
NM_002880.3:c.1763G>A , LRG_413t1:c.1763G>A (RAF1)	NP_002871.1:p.Cys588Tyr
XM_005265355.1:c.1763G>A (RAF1)	XP_005265412.1:p.Cys588Tyr
XM_005265357.1:c.1664G>A (RAF1)	XP_005265414.1:p.Cys555Tyr
XM_005265358.3:c.1520G>A (RAF1)	XP_005265415.1:p.Cys507Tyr
XM_005265359.3:c.1421G>A (RAF1)	XP_005265416.1:p.Cys474Tyr
XM_011533974.1:c.1763G>A (RAF1)	XP_011532276.1:p.Cys588Tyr
XM_011533975.1:c.1520G>A (RAF1)	XP_011532277.1:p.Cys507Tyr
NM_001354689.1:c.1823G>A (RAF1)	NP_001341618.1:p.Cys608Tyr
NM_001354690.1:c.1763G>A (RAF1)	NP_001341619.1:p.Cys588Tyr
NM_001354691.1:c.1520G>A (RAF1)	NP_001341620.1:p.Cys507Tyr
NM_001354692.1:c.1520G>A (RAF1)	NP_001341621.1:p.Cys507Tyr
NM_001354693.1:c.1664G>A (RAF1)	NP_001341622.1:p.Cys555Tyr
NM_001354694.1:c.1580G>A (RAF1)	NP_001341623.1:p.Cys527Tyr
NM_001354695.1:c.1421G>A (RAF1)	NP_001341624.1:p.Cys474Tyr
NR_148940.1:n.2291G>A (RAF1)
NR_148941.1:n.2237G>A (RAF1)
NR_148942.1:n.2176G>A (RAF1)
XM_011533974.3:c.1763G>A (RAF1)	XP_011532276.1:p.Cys588Tyr
XM_017006966.1:c.1664G>A (RAF1)	XP_016862455.1:p.Cys555Tyr
NM_001354689.3:c.1823G>A (RAF1)	NP_001341618.1:p.Cys608Tyr
NM_001354690.2:c.1763G>A (RAF1)	NP_001341619.1:p.Cys588Tyr
NM_001354691.2:c.1520G>A (RAF1)	NP_001341620.1:p.Cys507Tyr
NM_001354692.2:c.1520G>A (RAF1)	NP_001341621.1:p.Cys507Tyr
NM_001354693.2:c.1664G>A (RAF1)	NP_001341622.1:p.Cys555Tyr
NM_001354694.2:c.1580G>A (RAF1)	NP_001341623.1:p.Cys527Tyr
NM_001354695.2:c.1421G>A (RAF1)	NP_001341624.1:p.Cys474Tyr
NR_148940.2:n.2207G>A (RAF1)
NR_148941.2:n.2153G>A (RAF1)
NR_148942.2:n.2092G>A (RAF1)
NM_001354690.3:c.1763G>A (RAF1)	NP_001341619.1:p.Cys588Tyr
NM_001354691.3:c.1520G>A (RAF1)	NP_001341620.1:p.Cys507Tyr
NM_001354692.3:c.1520G>A (RAF1)	NP_001341621.1:p.Cys507Tyr
NM_001354693.3:c.1664G>A (RAF1)	NP_001341622.1:p.Cys555Tyr
NM_001354694.3:c.1580G>A (RAF1)	NP_001341623.1:p.Cys527Tyr
NM_001354695.3:c.1421G>A (RAF1)	NP_001341624.1:p.Cys474Tyr
NM_002880.4:c.1763G>A (RAF1) MANE Select	NP_002871.1:p.Cys588Tyr
NR_148940.3:n.2207G>A (RAF1)
NR_148941.3:n.2153G>A (RAF1)
NR_148942.3:n.2092G>A (RAF1)