Canonical Allele Identifier: CA351496759

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626418G>C (hg19) ; chr3:g.12584919G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584919G>C , CM000665.2:g.12584919G>C	GRCh38
NC_000003.11:g.12626418G>C , CM000665.1:g.12626418G>C	GRCh37
NC_000003.10:g.12601418G>C	NCBI36
NG_007467.1:g.84261C>G , LRG_413:g.84261C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1396C>G (RAF1)	ENSP00000401088.1:n.*1396C>G
ENST00000432427.3:c.1048C>G (RAF1)
ENST00000460610.2:n.6043C>G (RAF1)
ENST00000471449.2:n.541C>G (RAF1)
ENST00000475353.2:n.4011C>G (RAF1)
ENST00000684903.1:c.*1408C>G (RAF1)	ENSP00000508612.1:n.*1408C>G
ENST00000685348.1:c.*1442C>G (RAF1)	ENSP00000510285.1:n.*1442C>G
ENST00000685437.1:c.1632C>G (RAF1)	ENSP00000508794.1:p.Cys544Trp
ENST00000685653.1:c.1731C>G (RAF1)	ENSP00000509968.1:p.Cys577Trp
ENST00000685697.1:n.2466C>G (RAF1)
ENST00000685738.1:c.*695C>G (RAF1)	ENSP00000510156.1:n.*695C>G
ENST00000686409.1:n.5140C>G (RAF1)
ENST00000686455.1:n.4452C>G (RAF1)
ENST00000686762.1:c.*290C>G (RAF1)	ENSP00000509767.1:n.*290C>G
ENST00000687257.1:n.4185C>G (RAF1)
ENST00000687326.1:c.*3023C>G (RAF1)	ENSP00000509665.1:n.*3023C>G
ENST00000687505.1:n.1849C>G (RAF1)
ENST00000687923.1:c.1620C>G (RAF1)	ENSP00000510255.1:p.Cys540Trp
ENST00000688269.1:n.2327C>G (RAF1)
ENST00000688444.1:n.3848C>G (RAF1)
ENST00000688543.1:c.1632C>G (RAF1)	ENSP00000509612.1:p.Cys544Trp
ENST00000688625.1:c.*3100C>G (RAF1)	ENSP00000509522.1:n.*3100C>G
ENST00000688803.1:n.3159C>G (RAF1)
ENST00000688914.1:n.1144C>G (RAF1)
ENST00000689097.1:c.*1408C>G (RAF1)	ENSP00000509756.1:n.*1408C>G
ENST00000689389.1:c.1554C>G (RAF1)	ENSP00000510213.1:p.Cys518Trp
ENST00000689418.1:c.*3626C>G (RAF1)	ENSP00000509467.1:n.*3626C>G
ENST00000689540.1:n.4099C>G (RAF1)
ENST00000689876.1:c.*280C>G (RAF1)	ENSP00000508535.1:n.*280C>G
ENST00000689914.1:c.*665C>G (RAF1)	ENSP00000509847.1:n.*665C>G
ENST00000690397.1:c.1620C>G (RAF1)	ENSP00000508730.1:p.Cys540Trp
ENST00000690460.1:c.1719C>G (RAF1)	ENSP00000509106.1:p.Cys573Trp
ENST00000690585.1:c.457C>G (RAF1)
ENST00000690625.1:n.2767C>G (RAF1)
ENST00000691396.1:c.*1603C>G (RAF1)	ENSP00000510712.1:n.*1603C>G
ENST00000691643.1:n.2784C>G (RAF1)
ENST00000691724.1:c.*688C>G (RAF1)	ENSP00000509255.1:n.*688C>G
ENST00000691779.1:c.*1309C>G (RAF1)	ENSP00000508592.1:n.*1309C>G
ENST00000691888.1:c.605C>G (RAF1)
ENST00000691899.1:c.1731C>G (RAF1)	ENSP00000508763.1:p.Cys577Trp
ENST00000692069.1:n.4655C>G (RAF1)
ENST00000692093.1:c.1632C>G (RAF1)	ENSP00000509669.1:p.Cys544Trp
ENST00000692311.1:n.2555C>G (RAF1)
ENST00000692558.1:n.4314C>G (RAF1)
ENST00000692773.1:c.*1468C>G (RAF1)	ENSP00000509055.1:n.*1468C>G
ENST00000692830.1:c.*1476C>G (RAF1)	ENSP00000509461.1:n.*1476C>G
ENST00000693312.1:c.1506C>G (RAF1)	ENSP00000508686.1:p.Cys502Trp
ENST00000693664.1:c.*182C>G (RAF1)	ENSP00000509614.1:n.*182C>G
ENST00000693705.1:c.*1110C>G (RAF1)	ENSP00000510697.1:n.*1110C>G
ENST00000251849.9:c.1731C>G (RAF1) MANE Select	ENSP00000251849.4:p.Cys577Trp
ENST00000442415.7:c.1791C>G (RAF1)	ENSP00000401888.2:p.Cys597Trp
ENST00000676541.1:c.*2666G>C (MKRN2)	ENSP00000503730.1:n.*2666G>C
ENST00000677142.1:c.*2666G>C (MKRN2)	ENSP00000504455.1:n.*2666G>C
ENST00000677816.1:c.*1221G>C (MKRN2)	ENSP00000502893.1:n.*1221G>C
ENST00000677941.1:n.2729G>C (MKRN2)
ENST00000251849.8:c.1731C>G (RAF1)	ENSP00000251849.4:p.Cys577Trp
ENST00000423275.5:c.*1408C>G (RAF1)	ENSP00000401088.1:n.*1408C>G
ENST00000432427.2:c.1368C>G (RAF1)	ENSP00000398591.2:p.Cys456Trp
ENST00000442415.6:c.1791C>G (RAF1)	ENSP00000401888.2:p.Cys597Trp
ENST00000471449.1:n.420C>G (RAF1)
NM_002880.3:c.1731C>G , LRG_413t1:c.1731C>G (RAF1)	NP_002871.1:p.Cys577Trp
XM_005265355.1:c.1731C>G (RAF1)	XP_005265412.1:p.Cys577Trp
XM_005265357.1:c.1632C>G (RAF1)	XP_005265414.1:p.Cys544Trp
XM_005265358.3:c.1488C>G (RAF1)	XP_005265415.1:p.Cys496Trp
XM_005265359.3:c.1389C>G (RAF1)	XP_005265416.1:p.Cys463Trp
XM_011533974.1:c.1731C>G (RAF1)	XP_011532276.1:p.Cys577Trp
XM_011533975.1:c.1488C>G (RAF1)	XP_011532277.1:p.Cys496Trp
NM_001354689.1:c.1791C>G (RAF1)	NP_001341618.1:p.Cys597Trp
NM_001354690.1:c.1731C>G (RAF1)	NP_001341619.1:p.Cys577Trp
NM_001354691.1:c.1488C>G (RAF1)	NP_001341620.1:p.Cys496Trp
NM_001354692.1:c.1488C>G (RAF1)	NP_001341621.1:p.Cys496Trp
NM_001354693.1:c.1632C>G (RAF1)	NP_001341622.1:p.Cys544Trp
NM_001354694.1:c.1548C>G (RAF1)	NP_001341623.1:p.Cys516Trp
NM_001354695.1:c.1389C>G (RAF1)	NP_001341624.1:p.Cys463Trp
NR_148940.1:n.2259C>G (RAF1)
NR_148941.1:n.2205C>G (RAF1)
NR_148942.1:n.2144C>G (RAF1)
XM_011533974.3:c.1731C>G (RAF1)	XP_011532276.1:p.Cys577Trp
XM_017006966.1:c.1632C>G (RAF1)	XP_016862455.1:p.Cys544Trp
NM_001354689.3:c.1791C>G (RAF1)	NP_001341618.1:p.Cys597Trp
NM_001354690.2:c.1731C>G (RAF1)	NP_001341619.1:p.Cys577Trp
NM_001354691.2:c.1488C>G (RAF1)	NP_001341620.1:p.Cys496Trp
NM_001354692.2:c.1488C>G (RAF1)	NP_001341621.1:p.Cys496Trp
NM_001354693.2:c.1632C>G (RAF1)	NP_001341622.1:p.Cys544Trp
NM_001354694.2:c.1548C>G (RAF1)	NP_001341623.1:p.Cys516Trp
NM_001354695.2:c.1389C>G (RAF1)	NP_001341624.1:p.Cys463Trp
NR_148940.2:n.2175C>G (RAF1)
NR_148941.2:n.2121C>G (RAF1)
NR_148942.2:n.2060C>G (RAF1)
NM_001354690.3:c.1731C>G (RAF1)	NP_001341619.1:p.Cys577Trp
NM_001354691.3:c.1488C>G (RAF1)	NP_001341620.1:p.Cys496Trp
NM_001354692.3:c.1488C>G (RAF1)	NP_001341621.1:p.Cys496Trp
NM_001354693.3:c.1632C>G (RAF1)	NP_001341622.1:p.Cys544Trp
NM_001354694.3:c.1548C>G (RAF1)	NP_001341623.1:p.Cys516Trp
NM_001354695.3:c.1389C>G (RAF1)	NP_001341624.1:p.Cys463Trp
NM_002880.4:c.1731C>G (RAF1) MANE Select	NP_002871.1:p.Cys577Trp
NR_148940.3:n.2175C>G (RAF1)
NR_148941.3:n.2121C>G (RAF1)
NR_148942.3:n.2060C>G (RAF1)