Canonical Allele Identifier: CA351496098

Gene: RAF1 MKRN2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584626G>T , CM000665.2:g.12584626G>T	GRCh38
NC_000003.11:g.12626125G>T , CM000665.1:g.12626125G>T	GRCh37
NC_000003.10:g.12601125G>T	NCBI36
NG_007467.1:g.84554C>A , LRG_413:g.84554C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1500C>A (RAF1)	ENSP00000401088.1:n.*1500C>A
ENST00000432427.3:c.1152C>A (RAF1)
ENST00000460610.2:n.6147C>A (RAF1)
ENST00000471449.2:n.645C>A (RAF1)
ENST00000475353.2:n.4115C>A (RAF1)
ENST00000684903.1:c.*1512C>A (RAF1)	ENSP00000508612.1:n.*1512C>A
ENST00000685348.1:c.*1546C>A (RAF1)	ENSP00000510285.1:n.*1546C>A
ENST00000685437.1:c.1736C>A (RAF1)	ENSP00000508794.1:p.Ser579Tyr
ENST00000685653.1:c.1835C>A (RAF1)	ENSP00000509968.1:p.Ser612Tyr
ENST00000685697.1:n.2570C>A (RAF1)
ENST00000685738.1:c.*799C>A (RAF1)	ENSP00000510156.1:n.*799C>A
ENST00000686409.1:n.5244C>A (RAF1)
ENST00000686455.1:n.4556C>A (RAF1)
ENST00000686762.1:c.*394C>A (RAF1)	ENSP00000509767.1:n.*394C>A
ENST00000687257.1:n.4289C>A (RAF1)
ENST00000687326.1:c.*3127C>A (RAF1)	ENSP00000509665.1:n.*3127C>A
ENST00000687505.1:n.1953C>A (RAF1)
ENST00000687923.1:c.1724C>A (RAF1)	ENSP00000510255.1:p.Ser575Tyr
ENST00000688269.1:n.2431C>A (RAF1)
ENST00000688444.1:n.3952C>A (RAF1)
ENST00000688543.1:c.1736C>A (RAF1)	ENSP00000509612.1:p.Ser579Tyr
ENST00000688625.1:c.*3204C>A (RAF1)	ENSP00000509522.1:n.*3204C>A
ENST00000688803.1:n.3263C>A (RAF1)
ENST00000689097.1:c.*1512C>A (RAF1)	ENSP00000509756.1:n.*1512C>A
ENST00000689389.1:c.1658C>A (RAF1)	ENSP00000510213.1:p.Ser553Tyr
ENST00000689418.1:c.*3730C>A (RAF1)	ENSP00000509467.1:n.*3730C>A
ENST00000689540.1:n.4203C>A (RAF1)
ENST00000689876.1:c.*384C>A (RAF1)	ENSP00000508535.1:n.*384C>A
ENST00000689914.1:c.*769C>A (RAF1)	ENSP00000509847.1:n.*769C>A
ENST00000690397.1:c.1724C>A (RAF1)	ENSP00000508730.1:p.Ser575Tyr
ENST00000690460.1:c.1823C>A (RAF1)	ENSP00000509106.1:p.Ser608Tyr
ENST00000690585.1:c.561C>A (RAF1)
ENST00000690625.1:n.2871C>A (RAF1)
ENST00000691396.1:c.*1707C>A (RAF1)	ENSP00000510712.1:n.*1707C>A
ENST00000691643.1:n.2888C>A (RAF1)
ENST00000691724.1:c.*792C>A (RAF1)	ENSP00000509255.1:n.*792C>A
ENST00000691779.1:c.*1413C>A (RAF1)	ENSP00000508592.1:n.*1413C>A
ENST00000691888.1:c.709C>A (RAF1)
ENST00000691899.1:c.1835C>A (RAF1)	ENSP00000508763.1:p.Ser612Tyr
ENST00000692069.1:n.4759C>A (RAF1)
ENST00000692093.1:c.1736C>A (RAF1)	ENSP00000509669.1:p.Ser579Tyr
ENST00000692311.1:n.2659C>A (RAF1)
ENST00000692558.1:n.4418C>A (RAF1)
ENST00000692773.1:c.*1572C>A (RAF1)	ENSP00000509055.1:n.*1572C>A
ENST00000692830.1:c.*1580C>A (RAF1)	ENSP00000509461.1:n.*1580C>A
ENST00000693312.1:c.1610C>A (RAF1)	ENSP00000508686.1:p.Ser537Tyr
ENST00000693664.1:c.*286C>A (RAF1)	ENSP00000509614.1:n.*286C>A
ENST00000693705.1:c.*1214C>A (RAF1)	ENSP00000510697.1:n.*1214C>A
ENST00000251849.9:c.1835C>A (RAF1) MANE Select	ENSP00000251849.4:p.Ser612Tyr
ENST00000442415.7:c.1895C>A (RAF1)	ENSP00000401888.2:p.Ser632Tyr
ENST00000676541.1:c.*2373G>T (MKRN2)	ENSP00000503730.1:n.*2373G>T
ENST00000677142.1:c.*2373G>T (MKRN2)	ENSP00000504455.1:n.*2373G>T
ENST00000677816.1:c.*928G>T (MKRN2)	ENSP00000502893.1:n.*928G>T
ENST00000677941.1:n.2436G>T (MKRN2)
ENST00000251849.8:c.1835C>A (RAF1)	ENSP00000251849.4:p.Ser612Tyr
ENST00000423275.5:c.*1512C>A (RAF1)	ENSP00000401088.1:n.*1512C>A
ENST00000432427.2:c.1472C>A (RAF1)	ENSP00000398591.2:p.Ser491Tyr
ENST00000442415.6:c.1895C>A (RAF1)	ENSP00000401888.2:p.Ser632Tyr
ENST00000471449.1:n.524C>A (RAF1)
NM_002880.3:c.1835C>A , LRG_413t1:c.1835C>A (RAF1)	NP_002871.1:p.Ser612Tyr
XM_005265355.1:c.1835C>A (RAF1)	XP_005265412.1:p.Ser612Tyr
XM_005265357.1:c.1736C>A (RAF1)	XP_005265414.1:p.Ser579Tyr
XM_005265358.3:c.1592C>A (RAF1)	XP_005265415.1:p.Ser531Tyr
XM_005265359.3:c.1493C>A (RAF1)	XP_005265416.1:p.Ser498Tyr
XM_011533974.1:c.1835C>A (RAF1)	XP_011532276.1:p.Ser612Tyr
XM_011533975.1:c.1592C>A (RAF1)	XP_011532277.1:p.Ser531Tyr
NM_001354689.1:c.1895C>A (RAF1)	NP_001341618.1:p.Ser632Tyr
NM_001354690.1:c.1835C>A (RAF1)	NP_001341619.1:p.Ser612Tyr
NM_001354691.1:c.1592C>A (RAF1)	NP_001341620.1:p.Ser531Tyr
NM_001354692.1:c.1592C>A (RAF1)	NP_001341621.1:p.Ser531Tyr
NM_001354693.1:c.1736C>A (RAF1)	NP_001341622.1:p.Ser579Tyr
NM_001354694.1:c.1652C>A (RAF1)	NP_001341623.1:p.Ser551Tyr
NM_001354695.1:c.1493C>A (RAF1)	NP_001341624.1:p.Ser498Tyr
NR_148940.1:n.2363C>A (RAF1)
NR_148941.1:n.2309C>A (RAF1)
NR_148942.1:n.2248C>A (RAF1)
XM_011533974.3:c.1835C>A (RAF1)	XP_011532276.1:p.Ser612Tyr
XM_017006966.1:c.1736C>A (RAF1)	XP_016862455.1:p.Ser579Tyr
NM_001354689.3:c.1895C>A (RAF1)	NP_001341618.1:p.Ser632Tyr
NM_001354690.2:c.1835C>A (RAF1)	NP_001341619.1:p.Ser612Tyr
NM_001354691.2:c.1592C>A (RAF1)	NP_001341620.1:p.Ser531Tyr
NM_001354692.2:c.1592C>A (RAF1)	NP_001341621.1:p.Ser531Tyr
NM_001354693.2:c.1736C>A (RAF1)	NP_001341622.1:p.Ser579Tyr
NM_001354694.2:c.1652C>A (RAF1)	NP_001341623.1:p.Ser551Tyr
NM_001354695.2:c.1493C>A (RAF1)	NP_001341624.1:p.Ser498Tyr
NR_148940.2:n.2279C>A (RAF1)
NR_148941.2:n.2225C>A (RAF1)
NR_148942.2:n.2164C>A (RAF1)
NM_001354690.3:c.1835C>A (RAF1)	NP_001341619.1:p.Ser612Tyr
NM_001354691.3:c.1592C>A (RAF1)	NP_001341620.1:p.Ser531Tyr
NM_001354692.3:c.1592C>A (RAF1)	NP_001341621.1:p.Ser531Tyr
NM_001354693.3:c.1736C>A (RAF1)	NP_001341622.1:p.Ser579Tyr
NM_001354694.3:c.1652C>A (RAF1)	NP_001341623.1:p.Ser551Tyr
NM_001354695.3:c.1493C>A (RAF1)	NP_001341624.1:p.Ser498Tyr
NM_002880.4:c.1835C>A (RAF1) MANE Select	NP_002871.1:p.Ser612Tyr
NR_148940.3:n.2279C>A (RAF1)
NR_148941.3:n.2225C>A (RAF1)
NR_148942.3:n.2164C>A (RAF1)