Canonical Allele Identifier: CA351496760

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs2125319686
• MyVariant Identifiers: chr3:g.12626418G>T (hg19) ; chr3:g.12584919G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1396C>A (RAF1)	ENSP00000401088.1:n.*1396C>A
ENST00000432427.3:c.1048C>A (RAF1)
ENST00000460610.2:n.6043C>A (RAF1)
ENST00000471449.2:n.541C>A (RAF1)
ENST00000475353.2:n.4011C>A (RAF1)
ENST00000684903.1:c.*1408C>A (RAF1)	ENSP00000508612.1:n.*1408C>A
ENST00000685348.1:c.*1442C>A (RAF1)	ENSP00000510285.1:n.*1442C>A
ENST00000685437.1:c.1632C>A (RAF1)	ENSP00000508794.1:p.Cys544Ter
ENST00000685653.1:c.1731C>A (RAF1)	ENSP00000509968.1:p.Cys577Ter
ENST00000685697.1:n.2466C>A (RAF1)
ENST00000685738.1:c.*695C>A (RAF1)	ENSP00000510156.1:n.*695C>A
ENST00000686409.1:n.5140C>A (RAF1)
ENST00000686455.1:n.4452C>A (RAF1)
ENST00000686762.1:c.*290C>A (RAF1)	ENSP00000509767.1:n.*290C>A
ENST00000687257.1:n.4185C>A (RAF1)
ENST00000687326.1:c.*3023C>A (RAF1)	ENSP00000509665.1:n.*3023C>A
ENST00000687505.1:n.1849C>A (RAF1)
ENST00000687923.1:c.1620C>A (RAF1)	ENSP00000510255.1:p.Cys540Ter
ENST00000688269.1:n.2327C>A (RAF1)
ENST00000688444.1:n.3848C>A (RAF1)
ENST00000688543.1:c.1632C>A (RAF1)	ENSP00000509612.1:p.Cys544Ter
ENST00000688625.1:c.*3100C>A (RAF1)	ENSP00000509522.1:n.*3100C>A
ENST00000688803.1:n.3159C>A (RAF1)
ENST00000688914.1:n.1144C>A (RAF1)
ENST00000689097.1:c.*1408C>A (RAF1)	ENSP00000509756.1:n.*1408C>A
ENST00000689389.1:c.1554C>A (RAF1)	ENSP00000510213.1:p.Cys518Ter
ENST00000689418.1:c.*3626C>A (RAF1)	ENSP00000509467.1:n.*3626C>A
ENST00000689540.1:n.4099C>A (RAF1)
ENST00000689876.1:c.*280C>A (RAF1)	ENSP00000508535.1:n.*280C>A
ENST00000689914.1:c.*665C>A (RAF1)	ENSP00000509847.1:n.*665C>A
ENST00000690397.1:c.1620C>A (RAF1)	ENSP00000508730.1:p.Cys540Ter
ENST00000690460.1:c.1719C>A (RAF1)	ENSP00000509106.1:p.Cys573Ter
ENST00000690585.1:c.457C>A (RAF1)
ENST00000690625.1:n.2767C>A (RAF1)
ENST00000691396.1:c.*1603C>A (RAF1)	ENSP00000510712.1:n.*1603C>A
ENST00000691643.1:n.2784C>A (RAF1)
ENST00000691724.1:c.*688C>A (RAF1)	ENSP00000509255.1:n.*688C>A
ENST00000691779.1:c.*1309C>A (RAF1)	ENSP00000508592.1:n.*1309C>A
ENST00000691888.1:c.605C>A (RAF1)
ENST00000691899.1:c.1731C>A (RAF1)	ENSP00000508763.1:p.Cys577Ter
ENST00000692069.1:n.4655C>A (RAF1)
ENST00000692093.1:c.1632C>A (RAF1)	ENSP00000509669.1:p.Cys544Ter
ENST00000692311.1:n.2555C>A (RAF1)
ENST00000692558.1:n.4314C>A (RAF1)
ENST00000692773.1:c.*1468C>A (RAF1)	ENSP00000509055.1:n.*1468C>A
ENST00000692830.1:c.*1476C>A (RAF1)	ENSP00000509461.1:n.*1476C>A
ENST00000693312.1:c.1506C>A (RAF1)	ENSP00000508686.1:p.Cys502Ter
ENST00000693664.1:c.*182C>A (RAF1)	ENSP00000509614.1:n.*182C>A
ENST00000693705.1:c.*1110C>A (RAF1)	ENSP00000510697.1:n.*1110C>A
ENST00000251849.9:c.1731C>A (RAF1) MANE Select	ENSP00000251849.4:p.Cys577Ter
ENST00000442415.7:c.1791C>A (RAF1)	ENSP00000401888.2:p.Cys597Ter
ENST00000676541.1:c.*2666G>T (MKRN2)	ENSP00000503730.1:n.*2666G>T
ENST00000677142.1:c.*2666G>T (MKRN2)	ENSP00000504455.1:n.*2666G>T
ENST00000677816.1:c.*1221G>T (MKRN2)	ENSP00000502893.1:n.*1221G>T
ENST00000677941.1:n.2729G>T (MKRN2)
ENST00000251849.8:c.1731C>A (RAF1)	ENSP00000251849.4:p.Cys577Ter
ENST00000423275.5:c.*1408C>A (RAF1)	ENSP00000401088.1:n.*1408C>A
ENST00000432427.2:c.1368C>A (RAF1)	ENSP00000398591.2:p.Cys456Ter
ENST00000442415.6:c.1791C>A (RAF1)	ENSP00000401888.2:p.Cys597Ter
ENST00000471449.1:n.420C>A (RAF1)
NM_002880.3:c.1731C>A , LRG_413t1:c.1731C>A (RAF1)	NP_002871.1:p.Cys577Ter
XM_005265355.1:c.1731C>A (RAF1)	XP_005265412.1:p.Cys577Ter
XM_005265357.1:c.1632C>A (RAF1)	XP_005265414.1:p.Cys544Ter
XM_005265358.3:c.1488C>A (RAF1)	XP_005265415.1:p.Cys496Ter
XM_005265359.3:c.1389C>A (RAF1)	XP_005265416.1:p.Cys463Ter
XM_011533974.1:c.1731C>A (RAF1)	XP_011532276.1:p.Cys577Ter
XM_011533975.1:c.1488C>A (RAF1)	XP_011532277.1:p.Cys496Ter
NM_001354689.1:c.1791C>A (RAF1)	NP_001341618.1:p.Cys597Ter
NM_001354690.1:c.1731C>A (RAF1)	NP_001341619.1:p.Cys577Ter
NM_001354691.1:c.1488C>A (RAF1)	NP_001341620.1:p.Cys496Ter
NM_001354692.1:c.1488C>A (RAF1)	NP_001341621.1:p.Cys496Ter
NM_001354693.1:c.1632C>A (RAF1)	NP_001341622.1:p.Cys544Ter
NM_001354694.1:c.1548C>A (RAF1)	NP_001341623.1:p.Cys516Ter
NM_001354695.1:c.1389C>A (RAF1)	NP_001341624.1:p.Cys463Ter
NR_148940.1:n.2259C>A (RAF1)
NR_148941.1:n.2205C>A (RAF1)
NR_148942.1:n.2144C>A (RAF1)
XM_011533974.3:c.1731C>A (RAF1)	XP_011532276.1:p.Cys577Ter
XM_017006966.1:c.1632C>A (RAF1)	XP_016862455.1:p.Cys544Ter
NM_001354689.3:c.1791C>A (RAF1)	NP_001341618.1:p.Cys597Ter
NM_001354690.2:c.1731C>A (RAF1)	NP_001341619.1:p.Cys577Ter
NM_001354691.2:c.1488C>A (RAF1)	NP_001341620.1:p.Cys496Ter
NM_001354692.2:c.1488C>A (RAF1)	NP_001341621.1:p.Cys496Ter
NM_001354693.2:c.1632C>A (RAF1)	NP_001341622.1:p.Cys544Ter
NM_001354694.2:c.1548C>A (RAF1)	NP_001341623.1:p.Cys516Ter
NM_001354695.2:c.1389C>A (RAF1)	NP_001341624.1:p.Cys463Ter
NR_148940.2:n.2175C>A (RAF1)
NR_148941.2:n.2121C>A (RAF1)
NR_148942.2:n.2060C>A (RAF1)
NM_001354690.3:c.1731C>A (RAF1)	NP_001341619.1:p.Cys577Ter
NM_001354691.3:c.1488C>A (RAF1)	NP_001341620.1:p.Cys496Ter
NM_001354692.3:c.1488C>A (RAF1)	NP_001341621.1:p.Cys496Ter
NM_001354693.3:c.1632C>A (RAF1)	NP_001341622.1:p.Cys544Ter
NM_001354694.3:c.1548C>A (RAF1)	NP_001341623.1:p.Cys516Ter
NM_001354695.3:c.1389C>A (RAF1)	NP_001341624.1:p.Cys463Ter
NM_002880.4:c.1731C>A (RAF1) MANE Select	NP_002871.1:p.Cys577Ter
NR_148940.3:n.2175C>A (RAF1)
NR_148941.3:n.2121C>A (RAF1)
NR_148942.3:n.2060C>A (RAF1)