Canonical Allele Identifier: CA432522028

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626409T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584910T>G , CM000665.2:g.12584910T>G	GRCh38
NC_000003.11:g.12626409T>G , CM000665.1:g.12626409T>G	GRCh37
NC_000003.10:g.12601409T>G	NCBI36
NG_007467.1:g.84270A>C , LRG_413:g.84270A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1405A>C (RAF1)	ENSP00000401088.1:n.*1405A>C
ENST00000432427.3:c.1057A>C (RAF1)
ENST00000460610.2:n.6052A>C (RAF1)
ENST00000471449.2:n.550A>C (RAF1)
ENST00000475353.2:n.4020A>C (RAF1)
ENST00000684903.1:c.*1417A>C (RAF1)	ENSP00000508612.1:n.*1417A>C
ENST00000685348.1:c.*1451A>C (RAF1)	ENSP00000510285.1:n.*1451A>C
ENST00000685437.1:c.1641A>C (RAF1)	ENSP00000508794.1:p.Ala547=
ENST00000685653.1:c.1740A>C (RAF1)	ENSP00000509968.1:p.Ala580=
ENST00000685697.1:n.2475A>C (RAF1)
ENST00000685738.1:c.*704A>C (RAF1)	ENSP00000510156.1:n.*704A>C
ENST00000686409.1:n.5149A>C (RAF1)
ENST00000686455.1:n.4461A>C (RAF1)
ENST00000686762.1:c.*299A>C (RAF1)	ENSP00000509767.1:n.*299A>C
ENST00000687257.1:n.4194A>C (RAF1)
ENST00000687326.1:c.*3032A>C (RAF1)	ENSP00000509665.1:n.*3032A>C
ENST00000687505.1:n.1858A>C (RAF1)
ENST00000687923.1:c.1629A>C (RAF1)	ENSP00000510255.1:p.Ala543=
ENST00000688269.1:n.2336A>C (RAF1)
ENST00000688444.1:n.3857A>C (RAF1)
ENST00000688543.1:c.1641A>C (RAF1)	ENSP00000509612.1:p.Ala547=
ENST00000688625.1:c.*3109A>C (RAF1)	ENSP00000509522.1:n.*3109A>C
ENST00000688803.1:n.3168A>C (RAF1)
ENST00000688914.1:n.1153A>C (RAF1)
ENST00000689097.1:c.*1417A>C (RAF1)	ENSP00000509756.1:n.*1417A>C
ENST00000689389.1:c.1563A>C (RAF1)	ENSP00000510213.1:p.Ala521=
ENST00000689418.1:c.*3635A>C (RAF1)	ENSP00000509467.1:n.*3635A>C
ENST00000689540.1:n.4108A>C (RAF1)
ENST00000689876.1:c.*289A>C (RAF1)	ENSP00000508535.1:n.*289A>C
ENST00000689914.1:c.*674A>C (RAF1)	ENSP00000509847.1:n.*674A>C
ENST00000690397.1:c.1629A>C (RAF1)	ENSP00000508730.1:p.Ala543=
ENST00000690460.1:c.1728A>C (RAF1)	ENSP00000509106.1:p.Ala576=
ENST00000690585.1:c.466A>C (RAF1)
ENST00000690625.1:n.2776A>C (RAF1)
ENST00000691396.1:c.*1612A>C (RAF1)	ENSP00000510712.1:n.*1612A>C
ENST00000691643.1:n.2793A>C (RAF1)
ENST00000691724.1:c.*697A>C (RAF1)	ENSP00000509255.1:n.*697A>C
ENST00000691779.1:c.*1318A>C (RAF1)	ENSP00000508592.1:n.*1318A>C
ENST00000691888.1:c.614A>C (RAF1)
ENST00000691899.1:c.1740A>C (RAF1)	ENSP00000508763.1:p.Ala580=
ENST00000692069.1:n.4664A>C (RAF1)
ENST00000692093.1:c.1641A>C (RAF1)	ENSP00000509669.1:p.Ala547=
ENST00000692311.1:n.2564A>C (RAF1)
ENST00000692558.1:n.4323A>C (RAF1)
ENST00000692773.1:c.*1477A>C (RAF1)	ENSP00000509055.1:n.*1477A>C
ENST00000692830.1:c.*1485A>C (RAF1)	ENSP00000509461.1:n.*1485A>C
ENST00000693312.1:c.1515A>C (RAF1)	ENSP00000508686.1:p.Ala505=
ENST00000693664.1:c.*191A>C (RAF1)	ENSP00000509614.1:n.*191A>C
ENST00000693705.1:c.*1119A>C (RAF1)	ENSP00000510697.1:n.*1119A>C
ENST00000251849.9:c.1740A>C (RAF1) MANE Select	ENSP00000251849.4:p.Ala580=
ENST00000442415.7:c.1800A>C (RAF1)	ENSP00000401888.2:p.Ala600=
ENST00000676541.1:c.*2657T>G (MKRN2)	ENSP00000503730.1:n.*2657T>G
ENST00000677142.1:c.*2657T>G (MKRN2)	ENSP00000504455.1:n.*2657T>G
ENST00000677816.1:c.*1212T>G (MKRN2)	ENSP00000502893.1:n.*1212T>G
ENST00000677941.1:n.2720T>G (MKRN2)
ENST00000251849.8:c.1740A>C (RAF1)	ENSP00000251849.4:p.Ala580=
ENST00000423275.5:c.*1417A>C (RAF1)	ENSP00000401088.1:n.*1417A>C
ENST00000432427.2:c.1377A>C (RAF1)	ENSP00000398591.2:p.Ala459=
ENST00000442415.6:c.1800A>C (RAF1)	ENSP00000401888.2:p.Ala600=
ENST00000471449.1:n.429A>C (RAF1)
NM_002880.3:c.1740A>C , LRG_413t1:c.1740A>C (RAF1)	NP_002871.1:p.Ala580=
XM_005265355.1:c.1740A>C (RAF1)	XP_005265412.1:p.Ala580=
XM_005265357.1:c.1641A>C (RAF1)	XP_005265414.1:p.Ala547=
XM_005265358.3:c.1497A>C (RAF1)	XP_005265415.1:p.Ala499=
XM_005265359.3:c.1398A>C (RAF1)	XP_005265416.1:p.Ala466=
XM_011533974.1:c.1740A>C (RAF1)	XP_011532276.1:p.Ala580=
XM_011533975.1:c.1497A>C (RAF1)	XP_011532277.1:p.Ala499=
NM_001354689.1:c.1800A>C (RAF1)	NP_001341618.1:p.Ala600=
NM_001354690.1:c.1740A>C (RAF1)	NP_001341619.1:p.Ala580=
NM_001354691.1:c.1497A>C (RAF1)	NP_001341620.1:p.Ala499=
NM_001354692.1:c.1497A>C (RAF1)	NP_001341621.1:p.Ala499=
NM_001354693.1:c.1641A>C (RAF1)	NP_001341622.1:p.Ala547=
NM_001354694.1:c.1557A>C (RAF1)	NP_001341623.1:p.Ala519=
NM_001354695.1:c.1398A>C (RAF1)	NP_001341624.1:p.Ala466=
NR_148940.1:n.2268A>C (RAF1)
NR_148941.1:n.2214A>C (RAF1)
NR_148942.1:n.2153A>C (RAF1)
XM_011533974.3:c.1740A>C (RAF1)	XP_011532276.1:p.Ala580=
XM_017006966.1:c.1641A>C (RAF1)	XP_016862455.1:p.Ala547=
NM_001354689.3:c.1800A>C (RAF1)	NP_001341618.1:p.Ala600=
NM_001354690.2:c.1740A>C (RAF1)	NP_001341619.1:p.Ala580=
NM_001354691.2:c.1497A>C (RAF1)	NP_001341620.1:p.Ala499=
NM_001354692.2:c.1497A>C (RAF1)	NP_001341621.1:p.Ala499=
NM_001354693.2:c.1641A>C (RAF1)	NP_001341622.1:p.Ala547=
NM_001354694.2:c.1557A>C (RAF1)	NP_001341623.1:p.Ala519=
NM_001354695.2:c.1398A>C (RAF1)	NP_001341624.1:p.Ala466=
NR_148940.2:n.2184A>C (RAF1)
NR_148941.2:n.2130A>C (RAF1)
NR_148942.2:n.2069A>C (RAF1)
NM_001354690.3:c.1740A>C (RAF1)	NP_001341619.1:p.Ala580=
NM_001354691.3:c.1497A>C (RAF1)	NP_001341620.1:p.Ala499=
NM_001354692.3:c.1497A>C (RAF1)	NP_001341621.1:p.Ala499=
NM_001354693.3:c.1641A>C (RAF1)	NP_001341622.1:p.Ala547=
NM_001354694.3:c.1557A>C (RAF1)	NP_001341623.1:p.Ala519=
NM_001354695.3:c.1398A>C (RAF1)	NP_001341624.1:p.Ala466=
NM_002880.4:c.1740A>C (RAF1) MANE Select	NP_002871.1:p.Ala580=
NR_148940.3:n.2184A>C (RAF1)
NR_148941.3:n.2130A>C (RAF1)
NR_148942.3:n.2069A>C (RAF1)