Canonical Allele Identifier: CA351496603

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626383A>G (hg19) ; chr3:g.12584884A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584884A>G , CM000665.2:g.12584884A>G	GRCh38
NC_000003.11:g.12626383A>G , CM000665.1:g.12626383A>G	GRCh37
NC_000003.10:g.12601383A>G	NCBI36
NG_007467.1:g.84296T>C , LRG_413:g.84296T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1431T>C (RAF1)	ENSP00000401088.1:n.*1431T>C
ENST00000432427.3:c.1083T>C (RAF1)
ENST00000460610.2:n.6078T>C (RAF1)
ENST00000471449.2:n.576T>C (RAF1)
ENST00000475353.2:n.4046T>C (RAF1)
ENST00000684903.1:c.*1443T>C (RAF1)	ENSP00000508612.1:n.*1443T>C
ENST00000685348.1:c.*1477T>C (RAF1)	ENSP00000510285.1:n.*1477T>C
ENST00000685437.1:c.1667T>C (RAF1)	ENSP00000508794.1:p.Val556Ala
ENST00000685653.1:c.1766T>C (RAF1)	ENSP00000509968.1:p.Val589Ala
ENST00000685697.1:n.2501T>C (RAF1)
ENST00000685738.1:c.*730T>C (RAF1)	ENSP00000510156.1:n.*730T>C
ENST00000686409.1:n.5175T>C (RAF1)
ENST00000686455.1:n.4487T>C (RAF1)
ENST00000686762.1:c.*325T>C (RAF1)	ENSP00000509767.1:n.*325T>C
ENST00000687257.1:n.4220T>C (RAF1)
ENST00000687326.1:c.*3058T>C (RAF1)	ENSP00000509665.1:n.*3058T>C
ENST00000687505.1:n.1884T>C (RAF1)
ENST00000687923.1:c.1655T>C (RAF1)	ENSP00000510255.1:p.Val552Ala
ENST00000688269.1:n.2362T>C (RAF1)
ENST00000688444.1:n.3883T>C (RAF1)
ENST00000688543.1:c.1667T>C (RAF1)	ENSP00000509612.1:p.Val556Ala
ENST00000688625.1:c.*3135T>C (RAF1)	ENSP00000509522.1:n.*3135T>C
ENST00000688803.1:n.3194T>C (RAF1)
ENST00000689097.1:c.*1443T>C (RAF1)	ENSP00000509756.1:n.*1443T>C
ENST00000689389.1:c.1589T>C (RAF1)	ENSP00000510213.1:p.Val530Ala
ENST00000689418.1:c.*3661T>C (RAF1)	ENSP00000509467.1:n.*3661T>C
ENST00000689540.1:n.4134T>C (RAF1)
ENST00000689876.1:c.*315T>C (RAF1)	ENSP00000508535.1:n.*315T>C
ENST00000689914.1:c.*700T>C (RAF1)	ENSP00000509847.1:n.*700T>C
ENST00000690397.1:c.1655T>C (RAF1)	ENSP00000508730.1:p.Val552Ala
ENST00000690460.1:c.1754T>C (RAF1)	ENSP00000509106.1:p.Val585Ala
ENST00000690585.1:c.492T>C (RAF1)
ENST00000690625.1:n.2802T>C (RAF1)
ENST00000691396.1:c.*1638T>C (RAF1)	ENSP00000510712.1:n.*1638T>C
ENST00000691643.1:n.2819T>C (RAF1)
ENST00000691724.1:c.*723T>C (RAF1)	ENSP00000509255.1:n.*723T>C
ENST00000691779.1:c.*1344T>C (RAF1)	ENSP00000508592.1:n.*1344T>C
ENST00000691888.1:c.640T>C (RAF1)
ENST00000691899.1:c.1766T>C (RAF1)	ENSP00000508763.1:p.Val589Ala
ENST00000692069.1:n.4690T>C (RAF1)
ENST00000692093.1:c.1667T>C (RAF1)	ENSP00000509669.1:p.Val556Ala
ENST00000692311.1:n.2590T>C (RAF1)
ENST00000692558.1:n.4349T>C (RAF1)
ENST00000692773.1:c.*1503T>C (RAF1)	ENSP00000509055.1:n.*1503T>C
ENST00000692830.1:c.*1511T>C (RAF1)	ENSP00000509461.1:n.*1511T>C
ENST00000693312.1:c.1541T>C (RAF1)	ENSP00000508686.1:p.Val514Ala
ENST00000693664.1:c.*217T>C (RAF1)	ENSP00000509614.1:n.*217T>C
ENST00000693705.1:c.*1145T>C (RAF1)	ENSP00000510697.1:n.*1145T>C
ENST00000251849.9:c.1766T>C (RAF1) MANE Select	ENSP00000251849.4:p.Val589Ala
ENST00000442415.7:c.1826T>C (RAF1)	ENSP00000401888.2:p.Val609Ala
ENST00000676541.1:c.*2631A>G (MKRN2)	ENSP00000503730.1:n.*2631A>G
ENST00000677142.1:c.*2631A>G (MKRN2)	ENSP00000504455.1:n.*2631A>G
ENST00000677816.1:c.*1186A>G (MKRN2)	ENSP00000502893.1:n.*1186A>G
ENST00000677941.1:n.2694A>G (MKRN2)
ENST00000251849.8:c.1766T>C (RAF1)	ENSP00000251849.4:p.Val589Ala
ENST00000423275.5:c.*1443T>C (RAF1)	ENSP00000401088.1:n.*1443T>C
ENST00000432427.2:c.1403T>C (RAF1)	ENSP00000398591.2:p.Val468Ala
ENST00000442415.6:c.1826T>C (RAF1)	ENSP00000401888.2:p.Val609Ala
ENST00000471449.1:n.455T>C (RAF1)
NM_002880.3:c.1766T>C , LRG_413t1:c.1766T>C (RAF1)	NP_002871.1:p.Val589Ala
XM_005265355.1:c.1766T>C (RAF1)	XP_005265412.1:p.Val589Ala
XM_005265357.1:c.1667T>C (RAF1)	XP_005265414.1:p.Val556Ala
XM_005265358.3:c.1523T>C (RAF1)	XP_005265415.1:p.Val508Ala
XM_005265359.3:c.1424T>C (RAF1)	XP_005265416.1:p.Val475Ala
XM_011533974.1:c.1766T>C (RAF1)	XP_011532276.1:p.Val589Ala
XM_011533975.1:c.1523T>C (RAF1)	XP_011532277.1:p.Val508Ala
NM_001354689.1:c.1826T>C (RAF1)	NP_001341618.1:p.Val609Ala
NM_001354690.1:c.1766T>C (RAF1)	NP_001341619.1:p.Val589Ala
NM_001354691.1:c.1523T>C (RAF1)	NP_001341620.1:p.Val508Ala
NM_001354692.1:c.1523T>C (RAF1)	NP_001341621.1:p.Val508Ala
NM_001354693.1:c.1667T>C (RAF1)	NP_001341622.1:p.Val556Ala
NM_001354694.1:c.1583T>C (RAF1)	NP_001341623.1:p.Val528Ala
NM_001354695.1:c.1424T>C (RAF1)	NP_001341624.1:p.Val475Ala
NR_148940.1:n.2294T>C (RAF1)
NR_148941.1:n.2240T>C (RAF1)
NR_148942.1:n.2179T>C (RAF1)
XM_011533974.3:c.1766T>C (RAF1)	XP_011532276.1:p.Val589Ala
XM_017006966.1:c.1667T>C (RAF1)	XP_016862455.1:p.Val556Ala
NM_001354689.3:c.1826T>C (RAF1)	NP_001341618.1:p.Val609Ala
NM_001354690.2:c.1766T>C (RAF1)	NP_001341619.1:p.Val589Ala
NM_001354691.2:c.1523T>C (RAF1)	NP_001341620.1:p.Val508Ala
NM_001354692.2:c.1523T>C (RAF1)	NP_001341621.1:p.Val508Ala
NM_001354693.2:c.1667T>C (RAF1)	NP_001341622.1:p.Val556Ala
NM_001354694.2:c.1583T>C (RAF1)	NP_001341623.1:p.Val528Ala
NM_001354695.2:c.1424T>C (RAF1)	NP_001341624.1:p.Val475Ala
NR_148940.2:n.2210T>C (RAF1)
NR_148941.2:n.2156T>C (RAF1)
NR_148942.2:n.2095T>C (RAF1)
NM_001354690.3:c.1766T>C (RAF1)	NP_001341619.1:p.Val589Ala
NM_001354691.3:c.1523T>C (RAF1)	NP_001341620.1:p.Val508Ala
NM_001354692.3:c.1523T>C (RAF1)	NP_001341621.1:p.Val508Ala
NM_001354693.3:c.1667T>C (RAF1)	NP_001341622.1:p.Val556Ala
NM_001354694.3:c.1583T>C (RAF1)	NP_001341623.1:p.Val528Ala
NM_001354695.3:c.1424T>C (RAF1)	NP_001341624.1:p.Val475Ala
NM_002880.4:c.1766T>C (RAF1) MANE Select	NP_002871.1:p.Val589Ala
NR_148940.3:n.2210T>C (RAF1)
NR_148941.3:n.2156T>C (RAF1)
NR_148942.3:n.2095T>C (RAF1)