Canonical Allele Identifier: CA432272871

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12627276T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585777T>C , CM000665.2:g.12585777T>C	GRCh38
NC_000003.11:g.12627276T>C , CM000665.1:g.12627276T>C	GRCh37
NC_000003.10:g.12602276T>C	NCBI36
NG_007467.1:g.83403A>G , LRG_413:g.83403A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1105A>G (RAF1)	ENSP00000401088.1:n.*1105A>G
ENST00000432427.3:c.757A>G (RAF1)
ENST00000460610.2:n.5185A>G (RAF1)
ENST00000471449.2:n.250A>G (RAF1)
ENST00000475353.2:n.3153A>G (RAF1)
ENST00000684903.1:c.*1117A>G (RAF1)	ENSP00000508612.1:n.*1117A>G
ENST00000685348.1:c.*1095-371A>G (RAF1)	ENSP00000510285.1:n.*1095-371A>G
ENST00000685437.1:c.1341A>G (RAF1)	ENSP00000508794.1:p.Leu447=
ENST00000685653.1:c.1440A>G (RAF1)	ENSP00000509968.1:p.Leu480=
ENST00000685697.1:n.2175A>G (RAF1)
ENST00000685738.1:c.*404A>G (RAF1)	ENSP00000510156.1:n.*404A>G
ENST00000686409.1:n.4282A>G (RAF1)
ENST00000686455.1:n.3594A>G (RAF1)
ENST00000686762.1:c.1460A>G (RAF1)	ENSP00000509767.1:p.Ter487=
ENST00000687257.1:n.3467A>G (RAF1)
ENST00000687326.1:c.*2165A>G (RAF1)	ENSP00000509665.1:n.*2165A>G
ENST00000687505.1:n.1558A>G (RAF1)
ENST00000687923.1:c.1329A>G (RAF1)	ENSP00000510255.1:p.Leu443=
ENST00000688269.1:n.2036A>G (RAF1)
ENST00000688444.1:n.3557A>G (RAF1)
ENST00000688543.1:c.1341A>G (RAF1)	ENSP00000509612.1:p.Leu447=
ENST00000688625.1:c.*2809A>G (RAF1)	ENSP00000509522.1:n.*2809A>G
ENST00000688803.1:n.2964+498A>G (RAF1)
ENST00000688914.1:n.426A>G (RAF1)
ENST00000689097.1:c.*1117A>G (RAF1)	ENSP00000509756.1:n.*1117A>G
ENST00000689389.1:c.1263A>G (RAF1)	ENSP00000510213.1:p.Leu421=
ENST00000689418.1:c.*2908A>G (RAF1)	ENSP00000509467.1:n.*2908A>G
ENST00000689540.1:n.3381A>G (RAF1)
ENST00000689876.1:c.1418-371A>G (RAF1)	ENSP00000508535.1:n.1418-371A>G
ENST00000689914.1:c.*374A>G (RAF1)	ENSP00000509847.1:n.*374A>G
ENST00000690397.1:c.1329A>G (RAF1)	ENSP00000508730.1:p.Leu443=
ENST00000690460.1:c.1428A>G (RAF1)	ENSP00000509106.1:p.Leu476=
ENST00000690585.1:c.263-524A>G (RAF1)
ENST00000690625.1:n.2476A>G (RAF1)
ENST00000691396.1:c.*1312A>G (RAF1)	ENSP00000510712.1:n.*1312A>G
ENST00000691643.1:n.2066A>G (RAF1)
ENST00000691724.1:c.*397A>G (RAF1)	ENSP00000509255.1:n.*397A>G
ENST00000691779.1:c.*1018A>G (RAF1)	ENSP00000508592.1:n.*1018A>G
ENST00000691888.1:c.314A>G (RAF1)
ENST00000691899.1:c.1440A>G (RAF1)	ENSP00000508763.1:p.Leu480=
ENST00000692069.1:n.3797A>G (RAF1)
ENST00000692093.1:c.1341A>G (RAF1)	ENSP00000509669.1:p.Leu447=
ENST00000692311.1:n.2264A>G (RAF1)
ENST00000692558.1:n.3596A>G (RAF1)
ENST00000692773.1:c.*1177A>G (RAF1)	ENSP00000509055.1:n.*1177A>G
ENST00000692830.1:c.*1185A>G (RAF1)	ENSP00000509461.1:n.*1185A>G
ENST00000693312.1:c.1215A>G (RAF1)	ENSP00000508686.1:p.Leu405=
ENST00000693664.1:c.1487+498A>G (RAF1)	ENSP00000509614.1:n.1487+498A>G
ENST00000693705.1:c.*1048-796A>G (RAF1)	ENSP00000510697.1:n.*1048-796A>G
ENST00000251849.9:c.1440A>G (RAF1) MANE Select	ENSP00000251849.4:p.Leu480=
ENST00000442415.7:c.1500A>G (RAF1)	ENSP00000401888.2:p.Leu500=
ENST00000676541.1:c.*3524T>C (MKRN2)	ENSP00000503730.1:n.*3524T>C
ENST00000677142.1:c.*3524T>C (MKRN2)	ENSP00000504455.1:n.*3524T>C
ENST00000677816.1:c.*2079T>C (MKRN2)	ENSP00000502893.1:n.*2079T>C
ENST00000677941.1:n.3587T>C (MKRN2)
ENST00000251849.8:c.1440A>G (RAF1)	ENSP00000251849.4:p.Leu480=
ENST00000423275.5:c.*1117A>G (RAF1)	ENSP00000401088.1:n.*1117A>G
ENST00000432427.2:c.1077A>G (RAF1)	ENSP00000398591.2:p.Leu359=
ENST00000442415.6:c.1500A>G (RAF1)	ENSP00000401888.2:p.Leu500=
ENST00000471449.1:n.129A>G (RAF1)
NM_002880.3:c.1440A>G , LRG_413t1:c.1440A>G (RAF1)	NP_002871.1:p.Leu480=
XM_005265355.1:c.1440A>G (RAF1)	XP_005265412.1:p.Leu480=
XM_005265357.1:c.1341A>G (RAF1)	XP_005265414.1:p.Leu447=
XM_005265358.3:c.1197A>G (RAF1)	XP_005265415.1:p.Leu399=
XM_005265359.3:c.1098A>G (RAF1)	XP_005265416.1:p.Leu366=
XM_005265360.1:c.1418-371A>G (RAF1)	XP_005265417.1:n.1418-371A>G
XM_011533974.1:c.1440A>G (RAF1)	XP_011532276.1:p.Leu480=
XM_011533975.1:c.1197A>G (RAF1)	XP_011532277.1:p.Leu399=
NM_001354689.1:c.1500A>G (RAF1)	NP_001341618.1:p.Leu500=
NM_001354690.1:c.1440A>G (RAF1)	NP_001341619.1:p.Leu480=
NM_001354691.1:c.1197A>G (RAF1)	NP_001341620.1:p.Leu399=
NM_001354692.1:c.1197A>G (RAF1)	NP_001341621.1:p.Leu399=
NM_001354693.1:c.1341A>G (RAF1)	NP_001341622.1:p.Leu447=
NM_001354694.1:c.1257A>G (RAF1)	NP_001341623.1:p.Leu419=
NM_001354695.1:c.1098A>G (RAF1)	NP_001341624.1:p.Leu366=
NR_148940.1:n.1968A>G (RAF1)
NR_148941.1:n.1914A>G (RAF1)
NR_148942.1:n.1853A>G (RAF1)
XM_011533974.3:c.1440A>G (RAF1)	XP_011532276.1:p.Leu480=
XM_017006966.1:c.1341A>G (RAF1)	XP_016862455.1:p.Leu447=
NM_001354689.3:c.1500A>G (RAF1)	NP_001341618.1:p.Leu500=
NM_001354690.2:c.1440A>G (RAF1)	NP_001341619.1:p.Leu480=
NM_001354691.2:c.1197A>G (RAF1)	NP_001341620.1:p.Leu399=
NM_001354692.2:c.1197A>G (RAF1)	NP_001341621.1:p.Leu399=
NM_001354693.2:c.1341A>G (RAF1)	NP_001341622.1:p.Leu447=
NM_001354694.2:c.1257A>G (RAF1)	NP_001341623.1:p.Leu419=
NM_001354695.2:c.1098A>G (RAF1)	NP_001341624.1:p.Leu366=
NR_148940.2:n.1884A>G (RAF1)
NR_148941.2:n.1830A>G (RAF1)
NR_148942.2:n.1769A>G (RAF1)
NM_001354690.3:c.1440A>G (RAF1)	NP_001341619.1:p.Leu480=
NM_001354691.3:c.1197A>G (RAF1)	NP_001341620.1:p.Leu399=
NM_001354692.3:c.1197A>G (RAF1)	NP_001341621.1:p.Leu399=
NM_001354693.3:c.1341A>G (RAF1)	NP_001341622.1:p.Leu447=
NM_001354694.3:c.1257A>G (RAF1)	NP_001341623.1:p.Leu419=
NM_001354695.3:c.1098A>G (RAF1)	NP_001341624.1:p.Leu366=
NM_002880.4:c.1440A>G (RAF1) MANE Select	NP_002871.1:p.Leu480=
NR_148940.3:n.1884A>G (RAF1)
NR_148941.3:n.1830A>G (RAF1)
NR_148942.3:n.1769A>G (RAF1)