Canonical Allele Identifier: CA351497010

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626467A>G (hg19) ; chr3:g.12584968A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584968A>G , CM000665.2:g.12584968A>G	GRCh38
NC_000003.11:g.12626467A>G , CM000665.1:g.12626467A>G	GRCh37
NC_000003.10:g.12601467A>G	NCBI36
NG_007467.1:g.84212T>C , LRG_413:g.84212T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1347T>C (RAF1)	ENSP00000401088.1:n.*1347T>C
ENST00000432427.3:c.999T>C (RAF1)
ENST00000460610.2:n.5994T>C (RAF1)
ENST00000471449.2:n.492T>C (RAF1)
ENST00000475353.2:n.3962T>C (RAF1)
ENST00000684903.1:c.*1359T>C (RAF1)	ENSP00000508612.1:n.*1359T>C
ENST00000685348.1:c.*1393T>C (RAF1)	ENSP00000510285.1:n.*1393T>C
ENST00000685437.1:c.1583T>C (RAF1)	ENSP00000508794.1:p.Val528Ala
ENST00000685653.1:c.1682T>C (RAF1)	ENSP00000509968.1:p.Val561Ala
ENST00000685697.1:n.2417T>C (RAF1)
ENST00000685738.1:c.*646T>C (RAF1)	ENSP00000510156.1:n.*646T>C
ENST00000686409.1:n.5091T>C (RAF1)
ENST00000686455.1:n.4403T>C (RAF1)
ENST00000686762.1:c.*241T>C (RAF1)	ENSP00000509767.1:n.*241T>C
ENST00000687257.1:n.4136T>C (RAF1)
ENST00000687326.1:c.*2974T>C (RAF1)	ENSP00000509665.1:n.*2974T>C
ENST00000687505.1:n.1800T>C (RAF1)
ENST00000687923.1:c.1571T>C (RAF1)	ENSP00000510255.1:p.Val524Ala
ENST00000688269.1:n.2278T>C (RAF1)
ENST00000688444.1:n.3799T>C (RAF1)
ENST00000688543.1:c.1583T>C (RAF1)	ENSP00000509612.1:p.Val528Ala
ENST00000688625.1:c.*3051T>C (RAF1)	ENSP00000509522.1:n.*3051T>C
ENST00000688803.1:n.3110T>C (RAF1)
ENST00000688914.1:n.1095T>C (RAF1)
ENST00000689097.1:c.*1359T>C (RAF1)	ENSP00000509756.1:n.*1359T>C
ENST00000689389.1:c.1505T>C (RAF1)	ENSP00000510213.1:p.Val502Ala
ENST00000689418.1:c.*3577T>C (RAF1)	ENSP00000509467.1:n.*3577T>C
ENST00000689540.1:n.4050T>C (RAF1)
ENST00000689876.1:c.*231T>C (RAF1)	ENSP00000508535.1:n.*231T>C
ENST00000689914.1:c.*616T>C (RAF1)	ENSP00000509847.1:n.*616T>C
ENST00000690397.1:c.1571T>C (RAF1)	ENSP00000508730.1:p.Val524Ala
ENST00000690460.1:c.1670T>C (RAF1)	ENSP00000509106.1:p.Val557Ala
ENST00000690585.1:c.408T>C (RAF1)
ENST00000690625.1:n.2718T>C (RAF1)
ENST00000691396.1:c.*1554T>C (RAF1)	ENSP00000510712.1:n.*1554T>C
ENST00000691643.1:n.2735T>C (RAF1)
ENST00000691724.1:c.*639T>C (RAF1)	ENSP00000509255.1:n.*639T>C
ENST00000691779.1:c.*1260T>C (RAF1)	ENSP00000508592.1:n.*1260T>C
ENST00000691888.1:c.556T>C (RAF1)
ENST00000691899.1:c.1682T>C (RAF1)	ENSP00000508763.1:p.Val561Ala
ENST00000692069.1:n.4606T>C (RAF1)
ENST00000692093.1:c.1583T>C (RAF1)	ENSP00000509669.1:p.Val528Ala
ENST00000692311.1:n.2506T>C (RAF1)
ENST00000692558.1:n.4265T>C (RAF1)
ENST00000692773.1:c.*1419T>C (RAF1)	ENSP00000509055.1:n.*1419T>C
ENST00000692830.1:c.*1427T>C (RAF1)	ENSP00000509461.1:n.*1427T>C
ENST00000693312.1:c.1457T>C (RAF1)	ENSP00000508686.1:p.Val486Ala
ENST00000693664.1:c.*133T>C (RAF1)	ENSP00000509614.1:n.*133T>C
ENST00000693705.1:c.*1061T>C (RAF1)	ENSP00000510697.1:n.*1061T>C
ENST00000251849.9:c.1682T>C (RAF1) MANE Select	ENSP00000251849.4:p.Val561Ala
ENST00000442415.7:c.1742T>C (RAF1)	ENSP00000401888.2:p.Val581Ala
ENST00000676541.1:c.*2715A>G (MKRN2)	ENSP00000503730.1:n.*2715A>G
ENST00000677142.1:c.*2715A>G (MKRN2)	ENSP00000504455.1:n.*2715A>G
ENST00000677816.1:c.*1270A>G (MKRN2)	ENSP00000502893.1:n.*1270A>G
ENST00000677941.1:n.2778A>G (MKRN2)
ENST00000251849.8:c.1682T>C (RAF1)	ENSP00000251849.4:p.Val561Ala
ENST00000423275.5:c.*1359T>C (RAF1)	ENSP00000401088.1:n.*1359T>C
ENST00000432427.2:c.1319T>C (RAF1)	ENSP00000398591.2:p.Val440Ala
ENST00000442415.6:c.1742T>C (RAF1)	ENSP00000401888.2:p.Val581Ala
ENST00000471449.1:n.371T>C (RAF1)
NM_002880.3:c.1682T>C , LRG_413t1:c.1682T>C (RAF1)	NP_002871.1:p.Val561Ala
XM_005265355.1:c.1682T>C (RAF1)	XP_005265412.1:p.Val561Ala
XM_005265357.1:c.1583T>C (RAF1)	XP_005265414.1:p.Val528Ala
XM_005265358.3:c.1439T>C (RAF1)	XP_005265415.1:p.Val480Ala
XM_005265359.3:c.1340T>C (RAF1)	XP_005265416.1:p.Val447Ala
XM_011533974.1:c.1682T>C (RAF1)	XP_011532276.1:p.Val561Ala
XM_011533975.1:c.1439T>C (RAF1)	XP_011532277.1:p.Val480Ala
NM_001354689.1:c.1742T>C (RAF1)	NP_001341618.1:p.Val581Ala
NM_001354690.1:c.1682T>C (RAF1)	NP_001341619.1:p.Val561Ala
NM_001354691.1:c.1439T>C (RAF1)	NP_001341620.1:p.Val480Ala
NM_001354692.1:c.1439T>C (RAF1)	NP_001341621.1:p.Val480Ala
NM_001354693.1:c.1583T>C (RAF1)	NP_001341622.1:p.Val528Ala
NM_001354694.1:c.1499T>C (RAF1)	NP_001341623.1:p.Val500Ala
NM_001354695.1:c.1340T>C (RAF1)	NP_001341624.1:p.Val447Ala
NR_148940.1:n.2210T>C (RAF1)
NR_148941.1:n.2156T>C (RAF1)
NR_148942.1:n.2095T>C (RAF1)
XM_011533974.3:c.1682T>C (RAF1)	XP_011532276.1:p.Val561Ala
XM_017006966.1:c.1583T>C (RAF1)	XP_016862455.1:p.Val528Ala
NM_001354689.3:c.1742T>C (RAF1)	NP_001341618.1:p.Val581Ala
NM_001354690.2:c.1682T>C (RAF1)	NP_001341619.1:p.Val561Ala
NM_001354691.2:c.1439T>C (RAF1)	NP_001341620.1:p.Val480Ala
NM_001354692.2:c.1439T>C (RAF1)	NP_001341621.1:p.Val480Ala
NM_001354693.2:c.1583T>C (RAF1)	NP_001341622.1:p.Val528Ala
NM_001354694.2:c.1499T>C (RAF1)	NP_001341623.1:p.Val500Ala
NM_001354695.2:c.1340T>C (RAF1)	NP_001341624.1:p.Val447Ala
NR_148940.2:n.2126T>C (RAF1)
NR_148941.2:n.2072T>C (RAF1)
NR_148942.2:n.2011T>C (RAF1)
NM_001354690.3:c.1682T>C (RAF1)	NP_001341619.1:p.Val561Ala
NM_001354691.3:c.1439T>C (RAF1)	NP_001341620.1:p.Val480Ala
NM_001354692.3:c.1439T>C (RAF1)	NP_001341621.1:p.Val480Ala
NM_001354693.3:c.1583T>C (RAF1)	NP_001341622.1:p.Val528Ala
NM_001354694.3:c.1499T>C (RAF1)	NP_001341623.1:p.Val500Ala
NM_001354695.3:c.1340T>C (RAF1)	NP_001341624.1:p.Val447Ala
NM_002880.4:c.1682T>C (RAF1) MANE Select	NP_002871.1:p.Val561Ala
NR_148940.3:n.2126T>C (RAF1)
NR_148941.3:n.2072T>C (RAF1)
NR_148942.3:n.2011T>C (RAF1)