Canonical Allele Identifier: CA351499215

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12627274G>T (hg19) ; chr3:g.12585775G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585775G>T , CM000665.2:g.12585775G>T	GRCh38
NC_000003.11:g.12627274G>T , CM000665.1:g.12627274G>T	GRCh37
NC_000003.10:g.12602274G>T	NCBI36
NG_007467.1:g.83405C>A , LRG_413:g.83405C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1107C>A (RAF1)	ENSP00000401088.1:n.*1107C>A
ENST00000432427.3:c.759C>A (RAF1)
ENST00000460610.2:n.5187C>A (RAF1)
ENST00000471449.2:n.252C>A (RAF1)
ENST00000475353.2:n.3155C>A (RAF1)
ENST00000684903.1:c.*1119C>A (RAF1)	ENSP00000508612.1:n.*1119C>A
ENST00000685348.1:c.*1095-369C>A (RAF1)	ENSP00000510285.1:n.*1095-369C>A
ENST00000685437.1:c.1343C>A (RAF1)	ENSP00000508794.1:p.Thr448Lys
ENST00000685653.1:c.1442C>A (RAF1)	ENSP00000509968.1:p.Thr481Lys
ENST00000685697.1:n.2177C>A (RAF1)
ENST00000685738.1:c.*406C>A (RAF1)	ENSP00000510156.1:n.*406C>A
ENST00000686409.1:n.4284C>A (RAF1)
ENST00000686455.1:n.3596C>A (RAF1)
ENST00000686762.1:c.*1C>A (RAF1)	ENSP00000509767.1:n.*1C>A
ENST00000687257.1:n.3469C>A (RAF1)
ENST00000687326.1:c.*2167C>A (RAF1)	ENSP00000509665.1:n.*2167C>A
ENST00000687505.1:n.1560C>A (RAF1)
ENST00000687923.1:c.1331C>A (RAF1)	ENSP00000510255.1:p.Thr444Lys
ENST00000688269.1:n.2038C>A (RAF1)
ENST00000688444.1:n.3559C>A (RAF1)
ENST00000688543.1:c.1343C>A (RAF1)	ENSP00000509612.1:p.Thr448Lys
ENST00000688625.1:c.*2811C>A (RAF1)	ENSP00000509522.1:n.*2811C>A
ENST00000688803.1:n.2964+500C>A (RAF1)
ENST00000688914.1:n.428C>A (RAF1)
ENST00000689097.1:c.*1119C>A (RAF1)	ENSP00000509756.1:n.*1119C>A
ENST00000689389.1:c.1265C>A (RAF1)	ENSP00000510213.1:p.Thr422Lys
ENST00000689418.1:c.*2910C>A (RAF1)	ENSP00000509467.1:n.*2910C>A
ENST00000689540.1:n.3383C>A (RAF1)
ENST00000689876.1:c.1418-369C>A (RAF1)	ENSP00000508535.1:n.1418-369C>A
ENST00000689914.1:c.*376C>A (RAF1)	ENSP00000509847.1:n.*376C>A
ENST00000690397.1:c.1331C>A (RAF1)	ENSP00000508730.1:p.Thr444Lys
ENST00000690460.1:c.1430C>A (RAF1)	ENSP00000509106.1:p.Thr477Lys
ENST00000690585.1:c.263-522C>A (RAF1)
ENST00000690625.1:n.2478C>A (RAF1)
ENST00000691396.1:c.*1314C>A (RAF1)	ENSP00000510712.1:n.*1314C>A
ENST00000691643.1:n.2068C>A (RAF1)
ENST00000691724.1:c.*399C>A (RAF1)	ENSP00000509255.1:n.*399C>A
ENST00000691779.1:c.*1020C>A (RAF1)	ENSP00000508592.1:n.*1020C>A
ENST00000691888.1:c.316C>A (RAF1)
ENST00000691899.1:c.1442C>A (RAF1)	ENSP00000508763.1:p.Thr481Lys
ENST00000692069.1:n.3799C>A (RAF1)
ENST00000692093.1:c.1343C>A (RAF1)	ENSP00000509669.1:p.Thr448Lys
ENST00000692311.1:n.2266C>A (RAF1)
ENST00000692558.1:n.3598C>A (RAF1)
ENST00000692773.1:c.*1179C>A (RAF1)	ENSP00000509055.1:n.*1179C>A
ENST00000692830.1:c.*1187C>A (RAF1)	ENSP00000509461.1:n.*1187C>A
ENST00000693312.1:c.1217C>A (RAF1)	ENSP00000508686.1:p.Thr406Lys
ENST00000693664.1:c.1487+500C>A (RAF1)	ENSP00000509614.1:n.1487+500C>A
ENST00000693705.1:c.*1048-794C>A (RAF1)	ENSP00000510697.1:n.*1048-794C>A
ENST00000251849.9:c.1442C>A (RAF1) MANE Select	ENSP00000251849.4:p.Thr481Lys
ENST00000442415.7:c.1502C>A (RAF1)	ENSP00000401888.2:p.Thr501Lys
ENST00000676541.1:c.*3522G>T (MKRN2)	ENSP00000503730.1:n.*3522G>T
ENST00000677142.1:c.*3522G>T (MKRN2)	ENSP00000504455.1:n.*3522G>T
ENST00000677816.1:c.*2077G>T (MKRN2)	ENSP00000502893.1:n.*2077G>T
ENST00000677941.1:n.3585G>T (MKRN2)
ENST00000251849.8:c.1442C>A (RAF1)	ENSP00000251849.4:p.Thr481Lys
ENST00000423275.5:c.*1119C>A (RAF1)	ENSP00000401088.1:n.*1119C>A
ENST00000432427.2:c.1079C>A (RAF1)	ENSP00000398591.2:p.Thr360Lys
ENST00000442415.6:c.1502C>A (RAF1)	ENSP00000401888.2:p.Thr501Lys
ENST00000471449.1:n.131C>A (RAF1)
NM_002880.3:c.1442C>A , LRG_413t1:c.1442C>A (RAF1)	NP_002871.1:p.Thr481Lys
XM_005265355.1:c.1442C>A (RAF1)	XP_005265412.1:p.Thr481Lys
XM_005265357.1:c.1343C>A (RAF1)	XP_005265414.1:p.Thr448Lys
XM_005265358.3:c.1199C>A (RAF1)	XP_005265415.1:p.Thr400Lys
XM_005265359.3:c.1100C>A (RAF1)	XP_005265416.1:p.Thr367Lys
XM_005265360.1:c.1418-369C>A (RAF1)	XP_005265417.1:n.1418-369C>A
XM_011533974.1:c.1442C>A (RAF1)	XP_011532276.1:p.Thr481Lys
XM_011533975.1:c.1199C>A (RAF1)	XP_011532277.1:p.Thr400Lys
NM_001354689.1:c.1502C>A (RAF1)	NP_001341618.1:p.Thr501Lys
NM_001354690.1:c.1442C>A (RAF1)	NP_001341619.1:p.Thr481Lys
NM_001354691.1:c.1199C>A (RAF1)	NP_001341620.1:p.Thr400Lys
NM_001354692.1:c.1199C>A (RAF1)	NP_001341621.1:p.Thr400Lys
NM_001354693.1:c.1343C>A (RAF1)	NP_001341622.1:p.Thr448Lys
NM_001354694.1:c.1259C>A (RAF1)	NP_001341623.1:p.Thr420Lys
NM_001354695.1:c.1100C>A (RAF1)	NP_001341624.1:p.Thr367Lys
NR_148940.1:n.1970C>A (RAF1)
NR_148941.1:n.1916C>A (RAF1)
NR_148942.1:n.1855C>A (RAF1)
XM_011533974.3:c.1442C>A (RAF1)	XP_011532276.1:p.Thr481Lys
XM_017006966.1:c.1343C>A (RAF1)	XP_016862455.1:p.Thr448Lys
NM_001354689.3:c.1502C>A (RAF1)	NP_001341618.1:p.Thr501Lys
NM_001354690.2:c.1442C>A (RAF1)	NP_001341619.1:p.Thr481Lys
NM_001354691.2:c.1199C>A (RAF1)	NP_001341620.1:p.Thr400Lys
NM_001354692.2:c.1199C>A (RAF1)	NP_001341621.1:p.Thr400Lys
NM_001354693.2:c.1343C>A (RAF1)	NP_001341622.1:p.Thr448Lys
NM_001354694.2:c.1259C>A (RAF1)	NP_001341623.1:p.Thr420Lys
NM_001354695.2:c.1100C>A (RAF1)	NP_001341624.1:p.Thr367Lys
NR_148940.2:n.1886C>A (RAF1)
NR_148941.2:n.1832C>A (RAF1)
NR_148942.2:n.1771C>A (RAF1)
NM_001354690.3:c.1442C>A (RAF1)	NP_001341619.1:p.Thr481Lys
NM_001354691.3:c.1199C>A (RAF1)	NP_001341620.1:p.Thr400Lys
NM_001354692.3:c.1199C>A (RAF1)	NP_001341621.1:p.Thr400Lys
NM_001354693.3:c.1343C>A (RAF1)	NP_001341622.1:p.Thr448Lys
NM_001354694.3:c.1259C>A (RAF1)	NP_001341623.1:p.Thr420Lys
NM_001354695.3:c.1100C>A (RAF1)	NP_001341624.1:p.Thr367Lys
NM_002880.4:c.1442C>A (RAF1) MANE Select	NP_002871.1:p.Thr481Lys
NR_148940.3:n.1886C>A (RAF1)
NR_148941.3:n.1832C>A (RAF1)
NR_148942.3:n.1771C>A (RAF1)