Canonical Allele Identifier: CA432521997

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626358A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584859A>C , CM000665.2:g.12584859A>C	GRCh38
NC_000003.11:g.12626358A>C , CM000665.1:g.12626358A>C	GRCh37
NC_000003.10:g.12601358A>C	NCBI36
NG_007467.1:g.84321T>G , LRG_413:g.84321T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1456T>G (RAF1)	ENSP00000401088.1:n.*1456T>G
ENST00000432427.3:c.1108T>G (RAF1)
ENST00000460610.2:n.6103T>G (RAF1)
ENST00000471449.2:n.601T>G (RAF1)
ENST00000475353.2:n.4071T>G (RAF1)
ENST00000684903.1:c.*1468T>G (RAF1)	ENSP00000508612.1:n.*1468T>G
ENST00000685348.1:c.*1502T>G (RAF1)	ENSP00000510285.1:n.*1502T>G
ENST00000685437.1:c.1692T>G (RAF1)	ENSP00000508794.1:p.Pro564=
ENST00000685653.1:c.1791T>G (RAF1)	ENSP00000509968.1:p.Pro597=
ENST00000685697.1:n.2526T>G (RAF1)
ENST00000685738.1:c.*755T>G (RAF1)	ENSP00000510156.1:n.*755T>G
ENST00000686409.1:n.5200T>G (RAF1)
ENST00000686455.1:n.4512T>G (RAF1)
ENST00000686762.1:c.*350T>G (RAF1)	ENSP00000509767.1:n.*350T>G
ENST00000687257.1:n.4245T>G (RAF1)
ENST00000687326.1:c.*3083T>G (RAF1)	ENSP00000509665.1:n.*3083T>G
ENST00000687505.1:n.1909T>G (RAF1)
ENST00000687923.1:c.1680T>G (RAF1)	ENSP00000510255.1:p.Pro560=
ENST00000688269.1:n.2387T>G (RAF1)
ENST00000688444.1:n.3908T>G (RAF1)
ENST00000688543.1:c.1692T>G (RAF1)	ENSP00000509612.1:p.Pro564=
ENST00000688625.1:c.*3160T>G (RAF1)	ENSP00000509522.1:n.*3160T>G
ENST00000688803.1:n.3219T>G (RAF1)
ENST00000689097.1:c.*1468T>G (RAF1)	ENSP00000509756.1:n.*1468T>G
ENST00000689389.1:c.1614T>G (RAF1)	ENSP00000510213.1:p.Pro538=
ENST00000689418.1:c.*3686T>G (RAF1)	ENSP00000509467.1:n.*3686T>G
ENST00000689540.1:n.4159T>G (RAF1)
ENST00000689876.1:c.*340T>G (RAF1)	ENSP00000508535.1:n.*340T>G
ENST00000689914.1:c.*725T>G (RAF1)	ENSP00000509847.1:n.*725T>G
ENST00000690397.1:c.1680T>G (RAF1)	ENSP00000508730.1:p.Pro560=
ENST00000690460.1:c.1779T>G (RAF1)	ENSP00000509106.1:p.Pro593=
ENST00000690585.1:c.517T>G (RAF1)
ENST00000690625.1:n.2827T>G (RAF1)
ENST00000691396.1:c.*1663T>G (RAF1)	ENSP00000510712.1:n.*1663T>G
ENST00000691643.1:n.2844T>G (RAF1)
ENST00000691724.1:c.*748T>G (RAF1)	ENSP00000509255.1:n.*748T>G
ENST00000691779.1:c.*1369T>G (RAF1)	ENSP00000508592.1:n.*1369T>G
ENST00000691888.1:c.665T>G (RAF1)
ENST00000691899.1:c.1791T>G (RAF1)	ENSP00000508763.1:p.Pro597=
ENST00000692069.1:n.4715T>G (RAF1)
ENST00000692093.1:c.1692T>G (RAF1)	ENSP00000509669.1:p.Pro564=
ENST00000692311.1:n.2615T>G (RAF1)
ENST00000692558.1:n.4374T>G (RAF1)
ENST00000692773.1:c.*1528T>G (RAF1)	ENSP00000509055.1:n.*1528T>G
ENST00000692830.1:c.*1536T>G (RAF1)	ENSP00000509461.1:n.*1536T>G
ENST00000693312.1:c.1566T>G (RAF1)	ENSP00000508686.1:p.Pro522=
ENST00000693664.1:c.*242T>G (RAF1)	ENSP00000509614.1:n.*242T>G
ENST00000693705.1:c.*1170T>G (RAF1)	ENSP00000510697.1:n.*1170T>G
ENST00000251849.9:c.1791T>G (RAF1) MANE Select	ENSP00000251849.4:p.Pro597=
ENST00000442415.7:c.1851T>G (RAF1)	ENSP00000401888.2:p.Pro617=
ENST00000676541.1:c.*2606A>C (MKRN2)	ENSP00000503730.1:n.*2606A>C
ENST00000677142.1:c.*2606A>C (MKRN2)	ENSP00000504455.1:n.*2606A>C
ENST00000677816.1:c.*1161A>C (MKRN2)	ENSP00000502893.1:n.*1161A>C
ENST00000677941.1:n.2669A>C (MKRN2)
ENST00000251849.8:c.1791T>G (RAF1)	ENSP00000251849.4:p.Pro597=
ENST00000423275.5:c.*1468T>G (RAF1)	ENSP00000401088.1:n.*1468T>G
ENST00000432427.2:c.1428T>G (RAF1)	ENSP00000398591.2:p.Pro476=
ENST00000442415.6:c.1851T>G (RAF1)	ENSP00000401888.2:p.Pro617=
ENST00000471449.1:n.480T>G (RAF1)
NM_002880.3:c.1791T>G , LRG_413t1:c.1791T>G (RAF1)	NP_002871.1:p.Pro597=
XM_005265355.1:c.1791T>G (RAF1)	XP_005265412.1:p.Pro597=
XM_005265357.1:c.1692T>G (RAF1)	XP_005265414.1:p.Pro564=
XM_005265358.3:c.1548T>G (RAF1)	XP_005265415.1:p.Pro516=
XM_005265359.3:c.1449T>G (RAF1)	XP_005265416.1:p.Pro483=
XM_011533974.1:c.1791T>G (RAF1)	XP_011532276.1:p.Pro597=
XM_011533975.1:c.1548T>G (RAF1)	XP_011532277.1:p.Pro516=
NM_001354689.1:c.1851T>G (RAF1)	NP_001341618.1:p.Pro617=
NM_001354690.1:c.1791T>G (RAF1)	NP_001341619.1:p.Pro597=
NM_001354691.1:c.1548T>G (RAF1)	NP_001341620.1:p.Pro516=
NM_001354692.1:c.1548T>G (RAF1)	NP_001341621.1:p.Pro516=
NM_001354693.1:c.1692T>G (RAF1)	NP_001341622.1:p.Pro564=
NM_001354694.1:c.1608T>G (RAF1)	NP_001341623.1:p.Pro536=
NM_001354695.1:c.1449T>G (RAF1)	NP_001341624.1:p.Pro483=
NR_148940.1:n.2319T>G (RAF1)
NR_148941.1:n.2265T>G (RAF1)
NR_148942.1:n.2204T>G (RAF1)
XM_011533974.3:c.1791T>G (RAF1)	XP_011532276.1:p.Pro597=
XM_017006966.1:c.1692T>G (RAF1)	XP_016862455.1:p.Pro564=
NM_001354689.3:c.1851T>G (RAF1)	NP_001341618.1:p.Pro617=
NM_001354690.2:c.1791T>G (RAF1)	NP_001341619.1:p.Pro597=
NM_001354691.2:c.1548T>G (RAF1)	NP_001341620.1:p.Pro516=
NM_001354692.2:c.1548T>G (RAF1)	NP_001341621.1:p.Pro516=
NM_001354693.2:c.1692T>G (RAF1)	NP_001341622.1:p.Pro564=
NM_001354694.2:c.1608T>G (RAF1)	NP_001341623.1:p.Pro536=
NM_001354695.2:c.1449T>G (RAF1)	NP_001341624.1:p.Pro483=
NR_148940.2:n.2235T>G (RAF1)
NR_148941.2:n.2181T>G (RAF1)
NR_148942.2:n.2120T>G (RAF1)
NM_001354690.3:c.1791T>G (RAF1)	NP_001341619.1:p.Pro597=
NM_001354691.3:c.1548T>G (RAF1)	NP_001341620.1:p.Pro516=
NM_001354692.3:c.1548T>G (RAF1)	NP_001341621.1:p.Pro516=
NM_001354693.3:c.1692T>G (RAF1)	NP_001341622.1:p.Pro564=
NM_001354694.3:c.1608T>G (RAF1)	NP_001341623.1:p.Pro536=
NM_001354695.3:c.1449T>G (RAF1)	NP_001341624.1:p.Pro483=
NM_002880.4:c.1791T>G (RAF1) MANE Select	NP_002871.1:p.Pro597=
NR_148940.3:n.2235T>G (RAF1)
NR_148941.3:n.2181T>G (RAF1)
NR_148942.3:n.2120T>G (RAF1)