Canonical Allele Identifier: CA351496919

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626452G>T (hg19) ; chr3:g.12584953G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584953G>T , CM000665.2:g.12584953G>T	GRCh38
NC_000003.11:g.12626452G>T , CM000665.1:g.12626452G>T	GRCh37
NC_000003.10:g.12601452G>T	NCBI36
NG_007467.1:g.84227C>A , LRG_413:g.84227C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1362C>A (RAF1)	ENSP00000401088.1:n.*1362C>A
ENST00000432427.3:c.1014C>A (RAF1)
ENST00000460610.2:n.6009C>A (RAF1)
ENST00000471449.2:n.507C>A (RAF1)
ENST00000475353.2:n.3977C>A (RAF1)
ENST00000684903.1:c.*1374C>A (RAF1)	ENSP00000508612.1:n.*1374C>A
ENST00000685348.1:c.*1408C>A (RAF1)	ENSP00000510285.1:n.*1408C>A
ENST00000685437.1:c.1598C>A (RAF1)	ENSP00000508794.1:p.Ala533Asp
ENST00000685653.1:c.1697C>A (RAF1)	ENSP00000509968.1:p.Ala566Asp
ENST00000685697.1:n.2432C>A (RAF1)
ENST00000685738.1:c.*661C>A (RAF1)	ENSP00000510156.1:n.*661C>A
ENST00000686409.1:n.5106C>A (RAF1)
ENST00000686455.1:n.4418C>A (RAF1)
ENST00000686762.1:c.*256C>A (RAF1)	ENSP00000509767.1:n.*256C>A
ENST00000687257.1:n.4151C>A (RAF1)
ENST00000687326.1:c.*2989C>A (RAF1)	ENSP00000509665.1:n.*2989C>A
ENST00000687505.1:n.1815C>A (RAF1)
ENST00000687923.1:c.1586C>A (RAF1)	ENSP00000510255.1:p.Ala529Asp
ENST00000688269.1:n.2293C>A (RAF1)
ENST00000688444.1:n.3814C>A (RAF1)
ENST00000688543.1:c.1598C>A (RAF1)	ENSP00000509612.1:p.Ala533Asp
ENST00000688625.1:c.*3066C>A (RAF1)	ENSP00000509522.1:n.*3066C>A
ENST00000688803.1:n.3125C>A (RAF1)
ENST00000688914.1:n.1110C>A (RAF1)
ENST00000689097.1:c.*1374C>A (RAF1)	ENSP00000509756.1:n.*1374C>A
ENST00000689389.1:c.1520C>A (RAF1)	ENSP00000510213.1:p.Ala507Asp
ENST00000689418.1:c.*3592C>A (RAF1)	ENSP00000509467.1:n.*3592C>A
ENST00000689540.1:n.4065C>A (RAF1)
ENST00000689876.1:c.*246C>A (RAF1)	ENSP00000508535.1:n.*246C>A
ENST00000689914.1:c.*631C>A (RAF1)	ENSP00000509847.1:n.*631C>A
ENST00000690397.1:c.1586C>A (RAF1)	ENSP00000508730.1:p.Ala529Asp
ENST00000690460.1:c.1685C>A (RAF1)	ENSP00000509106.1:p.Ala562Asp
ENST00000690585.1:c.423C>A (RAF1)
ENST00000690625.1:n.2733C>A (RAF1)
ENST00000691396.1:c.*1569C>A (RAF1)	ENSP00000510712.1:n.*1569C>A
ENST00000691643.1:n.2750C>A (RAF1)
ENST00000691724.1:c.*654C>A (RAF1)	ENSP00000509255.1:n.*654C>A
ENST00000691779.1:c.*1275C>A (RAF1)	ENSP00000508592.1:n.*1275C>A
ENST00000691888.1:c.571C>A (RAF1)
ENST00000691899.1:c.1697C>A (RAF1)	ENSP00000508763.1:p.Ala566Asp
ENST00000692069.1:n.4621C>A (RAF1)
ENST00000692093.1:c.1598C>A (RAF1)	ENSP00000509669.1:p.Ala533Asp
ENST00000692311.1:n.2521C>A (RAF1)
ENST00000692558.1:n.4280C>A (RAF1)
ENST00000692773.1:c.*1434C>A (RAF1)	ENSP00000509055.1:n.*1434C>A
ENST00000692830.1:c.*1442C>A (RAF1)	ENSP00000509461.1:n.*1442C>A
ENST00000693312.1:c.1472C>A (RAF1)	ENSP00000508686.1:p.Ala491Asp
ENST00000693664.1:c.*148C>A (RAF1)	ENSP00000509614.1:n.*148C>A
ENST00000693705.1:c.*1076C>A (RAF1)	ENSP00000510697.1:n.*1076C>A
ENST00000251849.9:c.1697C>A (RAF1) MANE Select	ENSP00000251849.4:p.Ala566Asp
ENST00000442415.7:c.1757C>A (RAF1)	ENSP00000401888.2:p.Ala586Asp
ENST00000676541.1:c.*2700G>T (MKRN2)	ENSP00000503730.1:n.*2700G>T
ENST00000677142.1:c.*2700G>T (MKRN2)	ENSP00000504455.1:n.*2700G>T
ENST00000677816.1:c.*1255G>T (MKRN2)	ENSP00000502893.1:n.*1255G>T
ENST00000677941.1:n.2763G>T (MKRN2)
ENST00000251849.8:c.1697C>A (RAF1)	ENSP00000251849.4:p.Ala566Asp
ENST00000423275.5:c.*1374C>A (RAF1)	ENSP00000401088.1:n.*1374C>A
ENST00000432427.2:c.1334C>A (RAF1)	ENSP00000398591.2:p.Ala445Asp
ENST00000442415.6:c.1757C>A (RAF1)	ENSP00000401888.2:p.Ala586Asp
ENST00000471449.1:n.386C>A (RAF1)
NM_002880.3:c.1697C>A , LRG_413t1:c.1697C>A (RAF1)	NP_002871.1:p.Ala566Asp
XM_005265355.1:c.1697C>A (RAF1)	XP_005265412.1:p.Ala566Asp
XM_005265357.1:c.1598C>A (RAF1)	XP_005265414.1:p.Ala533Asp
XM_005265358.3:c.1454C>A (RAF1)	XP_005265415.1:p.Ala485Asp
XM_005265359.3:c.1355C>A (RAF1)	XP_005265416.1:p.Ala452Asp
XM_011533974.1:c.1697C>A (RAF1)	XP_011532276.1:p.Ala566Asp
XM_011533975.1:c.1454C>A (RAF1)	XP_011532277.1:p.Ala485Asp
NM_001354689.1:c.1757C>A (RAF1)	NP_001341618.1:p.Ala586Asp
NM_001354690.1:c.1697C>A (RAF1)	NP_001341619.1:p.Ala566Asp
NM_001354691.1:c.1454C>A (RAF1)	NP_001341620.1:p.Ala485Asp
NM_001354692.1:c.1454C>A (RAF1)	NP_001341621.1:p.Ala485Asp
NM_001354693.1:c.1598C>A (RAF1)	NP_001341622.1:p.Ala533Asp
NM_001354694.1:c.1514C>A (RAF1)	NP_001341623.1:p.Ala505Asp
NM_001354695.1:c.1355C>A (RAF1)	NP_001341624.1:p.Ala452Asp
NR_148940.1:n.2225C>A (RAF1)
NR_148941.1:n.2171C>A (RAF1)
NR_148942.1:n.2110C>A (RAF1)
XM_011533974.3:c.1697C>A (RAF1)	XP_011532276.1:p.Ala566Asp
XM_017006966.1:c.1598C>A (RAF1)	XP_016862455.1:p.Ala533Asp
NM_001354689.3:c.1757C>A (RAF1)	NP_001341618.1:p.Ala586Asp
NM_001354690.2:c.1697C>A (RAF1)	NP_001341619.1:p.Ala566Asp
NM_001354691.2:c.1454C>A (RAF1)	NP_001341620.1:p.Ala485Asp
NM_001354692.2:c.1454C>A (RAF1)	NP_001341621.1:p.Ala485Asp
NM_001354693.2:c.1598C>A (RAF1)	NP_001341622.1:p.Ala533Asp
NM_001354694.2:c.1514C>A (RAF1)	NP_001341623.1:p.Ala505Asp
NM_001354695.2:c.1355C>A (RAF1)	NP_001341624.1:p.Ala452Asp
NR_148940.2:n.2141C>A (RAF1)
NR_148941.2:n.2087C>A (RAF1)
NR_148942.2:n.2026C>A (RAF1)
NM_001354690.3:c.1697C>A (RAF1)	NP_001341619.1:p.Ala566Asp
NM_001354691.3:c.1454C>A (RAF1)	NP_001341620.1:p.Ala485Asp
NM_001354692.3:c.1454C>A (RAF1)	NP_001341621.1:p.Ala485Asp
NM_001354693.3:c.1598C>A (RAF1)	NP_001341622.1:p.Ala533Asp
NM_001354694.3:c.1514C>A (RAF1)	NP_001341623.1:p.Ala505Asp
NM_001354695.3:c.1355C>A (RAF1)	NP_001341624.1:p.Ala452Asp
NM_002880.4:c.1697C>A (RAF1) MANE Select	NP_002871.1:p.Ala566Asp
NR_148940.3:n.2141C>A (RAF1)
NR_148941.3:n.2087C>A (RAF1)
NR_148942.3:n.2026C>A (RAF1)