Canonical Allele Identifier: CA351499219

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12627275T>G (hg19) ; chr3:g.12585776T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585776T>G , CM000665.2:g.12585776T>G	GRCh38
NC_000003.11:g.12627275T>G , CM000665.1:g.12627275T>G	GRCh37
NC_000003.10:g.12602275T>G	NCBI36
NG_007467.1:g.83404A>C , LRG_413:g.83404A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1106A>C (RAF1)	ENSP00000401088.1:n.*1106A>C
ENST00000432427.3:c.758A>C (RAF1)
ENST00000460610.2:n.5186A>C (RAF1)
ENST00000471449.2:n.251A>C (RAF1)
ENST00000475353.2:n.3154A>C (RAF1)
ENST00000684903.1:c.*1118A>C (RAF1)	ENSP00000508612.1:n.*1118A>C
ENST00000685348.1:c.*1095-370A>C (RAF1)	ENSP00000510285.1:n.*1095-370A>C
ENST00000685437.1:c.1342A>C (RAF1)	ENSP00000508794.1:p.Thr448Pro
ENST00000685653.1:c.1441A>C (RAF1)	ENSP00000509968.1:p.Thr481Pro
ENST00000685697.1:n.2176A>C (RAF1)
ENST00000685738.1:c.*405A>C (RAF1)	ENSP00000510156.1:n.*405A>C
ENST00000686409.1:n.4283A>C (RAF1)
ENST00000686455.1:n.3595A>C (RAF1)
ENST00000686762.1:c.1461A>C (RAF1)	ENSP00000509767.1:p.Ter487Tyr
ENST00000687257.1:n.3468A>C (RAF1)
ENST00000687326.1:c.*2166A>C (RAF1)	ENSP00000509665.1:n.*2166A>C
ENST00000687505.1:n.1559A>C (RAF1)
ENST00000687923.1:c.1330A>C (RAF1)	ENSP00000510255.1:p.Thr444Pro
ENST00000688269.1:n.2037A>C (RAF1)
ENST00000688444.1:n.3558A>C (RAF1)
ENST00000688543.1:c.1342A>C (RAF1)	ENSP00000509612.1:p.Thr448Pro
ENST00000688625.1:c.*2810A>C (RAF1)	ENSP00000509522.1:n.*2810A>C
ENST00000688803.1:n.2964+499A>C (RAF1)
ENST00000688914.1:n.427A>C (RAF1)
ENST00000689097.1:c.*1118A>C (RAF1)	ENSP00000509756.1:n.*1118A>C
ENST00000689389.1:c.1264A>C (RAF1)	ENSP00000510213.1:p.Thr422Pro
ENST00000689418.1:c.*2909A>C (RAF1)	ENSP00000509467.1:n.*2909A>C
ENST00000689540.1:n.3382A>C (RAF1)
ENST00000689876.1:c.1418-370A>C (RAF1)	ENSP00000508535.1:n.1418-370A>C
ENST00000689914.1:c.*375A>C (RAF1)	ENSP00000509847.1:n.*375A>C
ENST00000690397.1:c.1330A>C (RAF1)	ENSP00000508730.1:p.Thr444Pro
ENST00000690460.1:c.1429A>C (RAF1)	ENSP00000509106.1:p.Thr477Pro
ENST00000690585.1:c.263-523A>C (RAF1)
ENST00000690625.1:n.2477A>C (RAF1)
ENST00000691396.1:c.*1313A>C (RAF1)	ENSP00000510712.1:n.*1313A>C
ENST00000691643.1:n.2067A>C (RAF1)
ENST00000691724.1:c.*398A>C (RAF1)	ENSP00000509255.1:n.*398A>C
ENST00000691779.1:c.*1019A>C (RAF1)	ENSP00000508592.1:n.*1019A>C
ENST00000691888.1:c.315A>C (RAF1)
ENST00000691899.1:c.1441A>C (RAF1)	ENSP00000508763.1:p.Thr481Pro
ENST00000692069.1:n.3798A>C (RAF1)
ENST00000692093.1:c.1342A>C (RAF1)	ENSP00000509669.1:p.Thr448Pro
ENST00000692311.1:n.2265A>C (RAF1)
ENST00000692558.1:n.3597A>C (RAF1)
ENST00000692773.1:c.*1178A>C (RAF1)	ENSP00000509055.1:n.*1178A>C
ENST00000692830.1:c.*1186A>C (RAF1)	ENSP00000509461.1:n.*1186A>C
ENST00000693312.1:c.1216A>C (RAF1)	ENSP00000508686.1:p.Thr406Pro
ENST00000693664.1:c.1487+499A>C (RAF1)	ENSP00000509614.1:n.1487+499A>C
ENST00000693705.1:c.*1048-795A>C (RAF1)	ENSP00000510697.1:n.*1048-795A>C
ENST00000251849.9:c.1441A>C (RAF1) MANE Select	ENSP00000251849.4:p.Thr481Pro
ENST00000442415.7:c.1501A>C (RAF1)	ENSP00000401888.2:p.Thr501Pro
ENST00000676541.1:c.*3523T>G (MKRN2)	ENSP00000503730.1:n.*3523T>G
ENST00000677142.1:c.*3523T>G (MKRN2)	ENSP00000504455.1:n.*3523T>G
ENST00000677816.1:c.*2078T>G (MKRN2)	ENSP00000502893.1:n.*2078T>G
ENST00000677941.1:n.3586T>G (MKRN2)
ENST00000251849.8:c.1441A>C (RAF1)	ENSP00000251849.4:p.Thr481Pro
ENST00000423275.5:c.*1118A>C (RAF1)	ENSP00000401088.1:n.*1118A>C
ENST00000432427.2:c.1078A>C (RAF1)	ENSP00000398591.2:p.Thr360Pro
ENST00000442415.6:c.1501A>C (RAF1)	ENSP00000401888.2:p.Thr501Pro
ENST00000471449.1:n.130A>C (RAF1)
NM_002880.3:c.1441A>C , LRG_413t1:c.1441A>C (RAF1)	NP_002871.1:p.Thr481Pro
XM_005265355.1:c.1441A>C (RAF1)	XP_005265412.1:p.Thr481Pro
XM_005265357.1:c.1342A>C (RAF1)	XP_005265414.1:p.Thr448Pro
XM_005265358.3:c.1198A>C (RAF1)	XP_005265415.1:p.Thr400Pro
XM_005265359.3:c.1099A>C (RAF1)	XP_005265416.1:p.Thr367Pro
XM_005265360.1:c.1418-370A>C (RAF1)	XP_005265417.1:n.1418-370A>C
XM_011533974.1:c.1441A>C (RAF1)	XP_011532276.1:p.Thr481Pro
XM_011533975.1:c.1198A>C (RAF1)	XP_011532277.1:p.Thr400Pro
NM_001354689.1:c.1501A>C (RAF1)	NP_001341618.1:p.Thr501Pro
NM_001354690.1:c.1441A>C (RAF1)	NP_001341619.1:p.Thr481Pro
NM_001354691.1:c.1198A>C (RAF1)	NP_001341620.1:p.Thr400Pro
NM_001354692.1:c.1198A>C (RAF1)	NP_001341621.1:p.Thr400Pro
NM_001354693.1:c.1342A>C (RAF1)	NP_001341622.1:p.Thr448Pro
NM_001354694.1:c.1258A>C (RAF1)	NP_001341623.1:p.Thr420Pro
NM_001354695.1:c.1099A>C (RAF1)	NP_001341624.1:p.Thr367Pro
NR_148940.1:n.1969A>C (RAF1)
NR_148941.1:n.1915A>C (RAF1)
NR_148942.1:n.1854A>C (RAF1)
XM_011533974.3:c.1441A>C (RAF1)	XP_011532276.1:p.Thr481Pro
XM_017006966.1:c.1342A>C (RAF1)	XP_016862455.1:p.Thr448Pro
NM_001354689.3:c.1501A>C (RAF1)	NP_001341618.1:p.Thr501Pro
NM_001354690.2:c.1441A>C (RAF1)	NP_001341619.1:p.Thr481Pro
NM_001354691.2:c.1198A>C (RAF1)	NP_001341620.1:p.Thr400Pro
NM_001354692.2:c.1198A>C (RAF1)	NP_001341621.1:p.Thr400Pro
NM_001354693.2:c.1342A>C (RAF1)	NP_001341622.1:p.Thr448Pro
NM_001354694.2:c.1258A>C (RAF1)	NP_001341623.1:p.Thr420Pro
NM_001354695.2:c.1099A>C (RAF1)	NP_001341624.1:p.Thr367Pro
NR_148940.2:n.1885A>C (RAF1)
NR_148941.2:n.1831A>C (RAF1)
NR_148942.2:n.1770A>C (RAF1)
NM_001354690.3:c.1441A>C (RAF1)	NP_001341619.1:p.Thr481Pro
NM_001354691.3:c.1198A>C (RAF1)	NP_001341620.1:p.Thr400Pro
NM_001354692.3:c.1198A>C (RAF1)	NP_001341621.1:p.Thr400Pro
NM_001354693.3:c.1342A>C (RAF1)	NP_001341622.1:p.Thr448Pro
NM_001354694.3:c.1258A>C (RAF1)	NP_001341623.1:p.Thr420Pro
NM_001354695.3:c.1099A>C (RAF1)	NP_001341624.1:p.Thr367Pro
NM_002880.4:c.1441A>C (RAF1) MANE Select	NP_002871.1:p.Thr481Pro
NR_148940.3:n.1885A>C (RAF1)
NR_148941.3:n.1831A>C (RAF1)
NR_148942.3:n.1770A>C (RAF1)