Canonical Allele Identifier: CA351496741

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626413T>G (hg19) ; chr3:g.12584914T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584914T>G , CM000665.2:g.12584914T>G	GRCh38
NC_000003.11:g.12626413T>G , CM000665.1:g.12626413T>G	GRCh37
NC_000003.10:g.12601413T>G	NCBI36
NG_007467.1:g.84266A>C , LRG_413:g.84266A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1401A>C (RAF1)	ENSP00000401088.1:n.*1401A>C
ENST00000432427.3:c.1053A>C (RAF1)
ENST00000460610.2:n.6048A>C (RAF1)
ENST00000471449.2:n.546A>C (RAF1)
ENST00000475353.2:n.4016A>C (RAF1)
ENST00000684903.1:c.*1413A>C (RAF1)	ENSP00000508612.1:n.*1413A>C
ENST00000685348.1:c.*1447A>C (RAF1)	ENSP00000510285.1:n.*1447A>C
ENST00000685437.1:c.1637A>C (RAF1)	ENSP00000508794.1:p.Lys546Thr
ENST00000685653.1:c.1736A>C (RAF1)	ENSP00000509968.1:p.Lys579Thr
ENST00000685697.1:n.2471A>C (RAF1)
ENST00000685738.1:c.*700A>C (RAF1)	ENSP00000510156.1:n.*700A>C
ENST00000686409.1:n.5145A>C (RAF1)
ENST00000686455.1:n.4457A>C (RAF1)
ENST00000686762.1:c.*295A>C (RAF1)	ENSP00000509767.1:n.*295A>C
ENST00000687257.1:n.4190A>C (RAF1)
ENST00000687326.1:c.*3028A>C (RAF1)	ENSP00000509665.1:n.*3028A>C
ENST00000687505.1:n.1854A>C (RAF1)
ENST00000687923.1:c.1625A>C (RAF1)	ENSP00000510255.1:p.Lys542Thr
ENST00000688269.1:n.2332A>C (RAF1)
ENST00000688444.1:n.3853A>C (RAF1)
ENST00000688543.1:c.1637A>C (RAF1)	ENSP00000509612.1:p.Lys546Thr
ENST00000688625.1:c.*3105A>C (RAF1)	ENSP00000509522.1:n.*3105A>C
ENST00000688803.1:n.3164A>C (RAF1)
ENST00000688914.1:n.1149A>C (RAF1)
ENST00000689097.1:c.*1413A>C (RAF1)	ENSP00000509756.1:n.*1413A>C
ENST00000689389.1:c.1559A>C (RAF1)	ENSP00000510213.1:p.Lys520Thr
ENST00000689418.1:c.*3631A>C (RAF1)	ENSP00000509467.1:n.*3631A>C
ENST00000689540.1:n.4104A>C (RAF1)
ENST00000689876.1:c.*285A>C (RAF1)	ENSP00000508535.1:n.*285A>C
ENST00000689914.1:c.*670A>C (RAF1)	ENSP00000509847.1:n.*670A>C
ENST00000690397.1:c.1625A>C (RAF1)	ENSP00000508730.1:p.Lys542Thr
ENST00000690460.1:c.1724A>C (RAF1)	ENSP00000509106.1:p.Lys575Thr
ENST00000690585.1:c.462A>C (RAF1)
ENST00000690625.1:n.2772A>C (RAF1)
ENST00000691396.1:c.*1608A>C (RAF1)	ENSP00000510712.1:n.*1608A>C
ENST00000691643.1:n.2789A>C (RAF1)
ENST00000691724.1:c.*693A>C (RAF1)	ENSP00000509255.1:n.*693A>C
ENST00000691779.1:c.*1314A>C (RAF1)	ENSP00000508592.1:n.*1314A>C
ENST00000691888.1:c.610A>C (RAF1)
ENST00000691899.1:c.1736A>C (RAF1)	ENSP00000508763.1:p.Lys579Thr
ENST00000692069.1:n.4660A>C (RAF1)
ENST00000692093.1:c.1637A>C (RAF1)	ENSP00000509669.1:p.Lys546Thr
ENST00000692311.1:n.2560A>C (RAF1)
ENST00000692558.1:n.4319A>C (RAF1)
ENST00000692773.1:c.*1473A>C (RAF1)	ENSP00000509055.1:n.*1473A>C
ENST00000692830.1:c.*1481A>C (RAF1)	ENSP00000509461.1:n.*1481A>C
ENST00000693312.1:c.1511A>C (RAF1)	ENSP00000508686.1:p.Lys504Thr
ENST00000693664.1:c.*187A>C (RAF1)	ENSP00000509614.1:n.*187A>C
ENST00000693705.1:c.*1115A>C (RAF1)	ENSP00000510697.1:n.*1115A>C
ENST00000251849.9:c.1736A>C (RAF1) MANE Select	ENSP00000251849.4:p.Lys579Thr
ENST00000442415.7:c.1796A>C (RAF1)	ENSP00000401888.2:p.Lys599Thr
ENST00000676541.1:c.*2661T>G (MKRN2)	ENSP00000503730.1:n.*2661T>G
ENST00000677142.1:c.*2661T>G (MKRN2)	ENSP00000504455.1:n.*2661T>G
ENST00000677816.1:c.*1216T>G (MKRN2)	ENSP00000502893.1:n.*1216T>G
ENST00000677941.1:n.2724T>G (MKRN2)
ENST00000251849.8:c.1736A>C (RAF1)	ENSP00000251849.4:p.Lys579Thr
ENST00000423275.5:c.*1413A>C (RAF1)	ENSP00000401088.1:n.*1413A>C
ENST00000432427.2:c.1373A>C (RAF1)	ENSP00000398591.2:p.Lys458Thr
ENST00000442415.6:c.1796A>C (RAF1)	ENSP00000401888.2:p.Lys599Thr
ENST00000471449.1:n.425A>C (RAF1)
NM_002880.3:c.1736A>C , LRG_413t1:c.1736A>C (RAF1)	NP_002871.1:p.Lys579Thr
XM_005265355.1:c.1736A>C (RAF1)	XP_005265412.1:p.Lys579Thr
XM_005265357.1:c.1637A>C (RAF1)	XP_005265414.1:p.Lys546Thr
XM_005265358.3:c.1493A>C (RAF1)	XP_005265415.1:p.Lys498Thr
XM_005265359.3:c.1394A>C (RAF1)	XP_005265416.1:p.Lys465Thr
XM_011533974.1:c.1736A>C (RAF1)	XP_011532276.1:p.Lys579Thr
XM_011533975.1:c.1493A>C (RAF1)	XP_011532277.1:p.Lys498Thr
NM_001354689.1:c.1796A>C (RAF1)	NP_001341618.1:p.Lys599Thr
NM_001354690.1:c.1736A>C (RAF1)	NP_001341619.1:p.Lys579Thr
NM_001354691.1:c.1493A>C (RAF1)	NP_001341620.1:p.Lys498Thr
NM_001354692.1:c.1493A>C (RAF1)	NP_001341621.1:p.Lys498Thr
NM_001354693.1:c.1637A>C (RAF1)	NP_001341622.1:p.Lys546Thr
NM_001354694.1:c.1553A>C (RAF1)	NP_001341623.1:p.Lys518Thr
NM_001354695.1:c.1394A>C (RAF1)	NP_001341624.1:p.Lys465Thr
NR_148940.1:n.2264A>C (RAF1)
NR_148941.1:n.2210A>C (RAF1)
NR_148942.1:n.2149A>C (RAF1)
XM_011533974.3:c.1736A>C (RAF1)	XP_011532276.1:p.Lys579Thr
XM_017006966.1:c.1637A>C (RAF1)	XP_016862455.1:p.Lys546Thr
NM_001354689.3:c.1796A>C (RAF1)	NP_001341618.1:p.Lys599Thr
NM_001354690.2:c.1736A>C (RAF1)	NP_001341619.1:p.Lys579Thr
NM_001354691.2:c.1493A>C (RAF1)	NP_001341620.1:p.Lys498Thr
NM_001354692.2:c.1493A>C (RAF1)	NP_001341621.1:p.Lys498Thr
NM_001354693.2:c.1637A>C (RAF1)	NP_001341622.1:p.Lys546Thr
NM_001354694.2:c.1553A>C (RAF1)	NP_001341623.1:p.Lys518Thr
NM_001354695.2:c.1394A>C (RAF1)	NP_001341624.1:p.Lys465Thr
NR_148940.2:n.2180A>C (RAF1)
NR_148941.2:n.2126A>C (RAF1)
NR_148942.2:n.2065A>C (RAF1)
NM_001354690.3:c.1736A>C (RAF1)	NP_001341619.1:p.Lys579Thr
NM_001354691.3:c.1493A>C (RAF1)	NP_001341620.1:p.Lys498Thr
NM_001354692.3:c.1493A>C (RAF1)	NP_001341621.1:p.Lys498Thr
NM_001354693.3:c.1637A>C (RAF1)	NP_001341622.1:p.Lys546Thr
NM_001354694.3:c.1553A>C (RAF1)	NP_001341623.1:p.Lys518Thr
NM_001354695.3:c.1394A>C (RAF1)	NP_001341624.1:p.Lys465Thr
NM_002880.4:c.1736A>C (RAF1) MANE Select	NP_002871.1:p.Lys579Thr
NR_148940.3:n.2180A>C (RAF1)
NR_148941.3:n.2126A>C (RAF1)
NR_148942.3:n.2065A>C (RAF1)