Canonical Allele Identifier: CA432522018

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626394T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584895T>G , CM000665.2:g.12584895T>G	GRCh38
NC_000003.11:g.12626394T>G , CM000665.1:g.12626394T>G	GRCh37
NC_000003.10:g.12601394T>G	NCBI36
NG_007467.1:g.84285A>C , LRG_413:g.84285A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1420A>C (RAF1)	ENSP00000401088.1:n.*1420A>C
ENST00000432427.3:c.1072A>C (RAF1)
ENST00000460610.2:n.6067A>C (RAF1)
ENST00000471449.2:n.565A>C (RAF1)
ENST00000475353.2:n.4035A>C (RAF1)
ENST00000684903.1:c.*1432A>C (RAF1)	ENSP00000508612.1:n.*1432A>C
ENST00000685348.1:c.*1466A>C (RAF1)	ENSP00000510285.1:n.*1466A>C
ENST00000685437.1:c.1656A>C (RAF1)	ENSP00000508794.1:p.Val552=
ENST00000685653.1:c.1755A>C (RAF1)	ENSP00000509968.1:p.Val585=
ENST00000685697.1:n.2490A>C (RAF1)
ENST00000685738.1:c.*719A>C (RAF1)	ENSP00000510156.1:n.*719A>C
ENST00000686409.1:n.5164A>C (RAF1)
ENST00000686455.1:n.4476A>C (RAF1)
ENST00000686762.1:c.*314A>C (RAF1)	ENSP00000509767.1:n.*314A>C
ENST00000687257.1:n.4209A>C (RAF1)
ENST00000687326.1:c.*3047A>C (RAF1)	ENSP00000509665.1:n.*3047A>C
ENST00000687505.1:n.1873A>C (RAF1)
ENST00000687923.1:c.1644A>C (RAF1)	ENSP00000510255.1:p.Val548=
ENST00000688269.1:n.2351A>C (RAF1)
ENST00000688444.1:n.3872A>C (RAF1)
ENST00000688543.1:c.1656A>C (RAF1)	ENSP00000509612.1:p.Val552=
ENST00000688625.1:c.*3124A>C (RAF1)	ENSP00000509522.1:n.*3124A>C
ENST00000688803.1:n.3183A>C (RAF1)
ENST00000688914.1:n.1168A>C (RAF1)
ENST00000689097.1:c.*1432A>C (RAF1)	ENSP00000509756.1:n.*1432A>C
ENST00000689389.1:c.1578A>C (RAF1)	ENSP00000510213.1:p.Val526=
ENST00000689418.1:c.*3650A>C (RAF1)	ENSP00000509467.1:n.*3650A>C
ENST00000689540.1:n.4123A>C (RAF1)
ENST00000689876.1:c.*304A>C (RAF1)	ENSP00000508535.1:n.*304A>C
ENST00000689914.1:c.*689A>C (RAF1)	ENSP00000509847.1:n.*689A>C
ENST00000690397.1:c.1644A>C (RAF1)	ENSP00000508730.1:p.Val548=
ENST00000690460.1:c.1743A>C (RAF1)	ENSP00000509106.1:p.Val581=
ENST00000690585.1:c.481A>C (RAF1)
ENST00000690625.1:n.2791A>C (RAF1)
ENST00000691396.1:c.*1627A>C (RAF1)	ENSP00000510712.1:n.*1627A>C
ENST00000691643.1:n.2808A>C (RAF1)
ENST00000691724.1:c.*712A>C (RAF1)	ENSP00000509255.1:n.*712A>C
ENST00000691779.1:c.*1333A>C (RAF1)	ENSP00000508592.1:n.*1333A>C
ENST00000691888.1:c.629A>C (RAF1)
ENST00000691899.1:c.1755A>C (RAF1)	ENSP00000508763.1:p.Val585=
ENST00000692069.1:n.4679A>C (RAF1)
ENST00000692093.1:c.1656A>C (RAF1)	ENSP00000509669.1:p.Val552=
ENST00000692311.1:n.2579A>C (RAF1)
ENST00000692558.1:n.4338A>C (RAF1)
ENST00000692773.1:c.*1492A>C (RAF1)	ENSP00000509055.1:n.*1492A>C
ENST00000692830.1:c.*1500A>C (RAF1)	ENSP00000509461.1:n.*1500A>C
ENST00000693312.1:c.1530A>C (RAF1)	ENSP00000508686.1:p.Val510=
ENST00000693664.1:c.*206A>C (RAF1)	ENSP00000509614.1:n.*206A>C
ENST00000693705.1:c.*1134A>C (RAF1)	ENSP00000510697.1:n.*1134A>C
ENST00000251849.9:c.1755A>C (RAF1) MANE Select	ENSP00000251849.4:p.Val585=
ENST00000442415.7:c.1815A>C (RAF1)	ENSP00000401888.2:p.Val605=
ENST00000676541.1:c.*2642T>G (MKRN2)	ENSP00000503730.1:n.*2642T>G
ENST00000677142.1:c.*2642T>G (MKRN2)	ENSP00000504455.1:n.*2642T>G
ENST00000677816.1:c.*1197T>G (MKRN2)	ENSP00000502893.1:n.*1197T>G
ENST00000677941.1:n.2705T>G (MKRN2)
ENST00000251849.8:c.1755A>C (RAF1)	ENSP00000251849.4:p.Val585=
ENST00000423275.5:c.*1432A>C (RAF1)	ENSP00000401088.1:n.*1432A>C
ENST00000432427.2:c.1392A>C (RAF1)	ENSP00000398591.2:p.Val464=
ENST00000442415.6:c.1815A>C (RAF1)	ENSP00000401888.2:p.Val605=
ENST00000471449.1:n.444A>C (RAF1)
NM_002880.3:c.1755A>C , LRG_413t1:c.1755A>C (RAF1)	NP_002871.1:p.Val585=
XM_005265355.1:c.1755A>C (RAF1)	XP_005265412.1:p.Val585=
XM_005265357.1:c.1656A>C (RAF1)	XP_005265414.1:p.Val552=
XM_005265358.3:c.1512A>C (RAF1)	XP_005265415.1:p.Val504=
XM_005265359.3:c.1413A>C (RAF1)	XP_005265416.1:p.Val471=
XM_011533974.1:c.1755A>C (RAF1)	XP_011532276.1:p.Val585=
XM_011533975.1:c.1512A>C (RAF1)	XP_011532277.1:p.Val504=
NM_001354689.1:c.1815A>C (RAF1)	NP_001341618.1:p.Val605=
NM_001354690.1:c.1755A>C (RAF1)	NP_001341619.1:p.Val585=
NM_001354691.1:c.1512A>C (RAF1)	NP_001341620.1:p.Val504=
NM_001354692.1:c.1512A>C (RAF1)	NP_001341621.1:p.Val504=
NM_001354693.1:c.1656A>C (RAF1)	NP_001341622.1:p.Val552=
NM_001354694.1:c.1572A>C (RAF1)	NP_001341623.1:p.Val524=
NM_001354695.1:c.1413A>C (RAF1)	NP_001341624.1:p.Val471=
NR_148940.1:n.2283A>C (RAF1)
NR_148941.1:n.2229A>C (RAF1)
NR_148942.1:n.2168A>C (RAF1)
XM_011533974.3:c.1755A>C (RAF1)	XP_011532276.1:p.Val585=
XM_017006966.1:c.1656A>C (RAF1)	XP_016862455.1:p.Val552=
NM_001354689.3:c.1815A>C (RAF1)	NP_001341618.1:p.Val605=
NM_001354690.2:c.1755A>C (RAF1)	NP_001341619.1:p.Val585=
NM_001354691.2:c.1512A>C (RAF1)	NP_001341620.1:p.Val504=
NM_001354692.2:c.1512A>C (RAF1)	NP_001341621.1:p.Val504=
NM_001354693.2:c.1656A>C (RAF1)	NP_001341622.1:p.Val552=
NM_001354694.2:c.1572A>C (RAF1)	NP_001341623.1:p.Val524=
NM_001354695.2:c.1413A>C (RAF1)	NP_001341624.1:p.Val471=
NR_148940.2:n.2199A>C (RAF1)
NR_148941.2:n.2145A>C (RAF1)
NR_148942.2:n.2084A>C (RAF1)
NM_001354690.3:c.1755A>C (RAF1)	NP_001341619.1:p.Val585=
NM_001354691.3:c.1512A>C (RAF1)	NP_001341620.1:p.Val504=
NM_001354692.3:c.1512A>C (RAF1)	NP_001341621.1:p.Val504=
NM_001354693.3:c.1656A>C (RAF1)	NP_001341622.1:p.Val552=
NM_001354694.3:c.1572A>C (RAF1)	NP_001341623.1:p.Val524=
NM_001354695.3:c.1413A>C (RAF1)	NP_001341624.1:p.Val471=
NM_002880.4:c.1755A>C (RAF1) MANE Select	NP_002871.1:p.Val585=
NR_148940.3:n.2199A>C (RAF1)
NR_148941.3:n.2145A>C (RAF1)
NR_148942.3:n.2084A>C (RAF1)