Canonical Allele Identifier: CA351496891

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626447G>C (hg19) ; chr3:g.12584948G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584948G>C , CM000665.2:g.12584948G>C	GRCh38
NC_000003.11:g.12626447G>C , CM000665.1:g.12626447G>C	GRCh37
NC_000003.10:g.12601447G>C	NCBI36
NG_007467.1:g.84232C>G , LRG_413:g.84232C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1367C>G (RAF1)	ENSP00000401088.1:n.*1367C>G
ENST00000432427.3:c.1019C>G (RAF1)
ENST00000460610.2:n.6014C>G (RAF1)
ENST00000471449.2:n.512C>G (RAF1)
ENST00000475353.2:n.3982C>G (RAF1)
ENST00000684903.1:c.*1379C>G (RAF1)	ENSP00000508612.1:n.*1379C>G
ENST00000685348.1:c.*1413C>G (RAF1)	ENSP00000510285.1:n.*1413C>G
ENST00000685437.1:c.1603C>G (RAF1)	ENSP00000508794.1:p.Pro535Ala
ENST00000685653.1:c.1702C>G (RAF1)	ENSP00000509968.1:p.Pro568Ala
ENST00000685697.1:n.2437C>G (RAF1)
ENST00000685738.1:c.*666C>G (RAF1)	ENSP00000510156.1:n.*666C>G
ENST00000686409.1:n.5111C>G (RAF1)
ENST00000686455.1:n.4423C>G (RAF1)
ENST00000686762.1:c.*261C>G (RAF1)	ENSP00000509767.1:n.*261C>G
ENST00000687257.1:n.4156C>G (RAF1)
ENST00000687326.1:c.*2994C>G (RAF1)	ENSP00000509665.1:n.*2994C>G
ENST00000687505.1:n.1820C>G (RAF1)
ENST00000687923.1:c.1591C>G (RAF1)	ENSP00000510255.1:p.Pro531Ala
ENST00000688269.1:n.2298C>G (RAF1)
ENST00000688444.1:n.3819C>G (RAF1)
ENST00000688543.1:c.1603C>G (RAF1)	ENSP00000509612.1:p.Pro535Ala
ENST00000688625.1:c.*3071C>G (RAF1)	ENSP00000509522.1:n.*3071C>G
ENST00000688803.1:n.3130C>G (RAF1)
ENST00000688914.1:n.1115C>G (RAF1)
ENST00000689097.1:c.*1379C>G (RAF1)	ENSP00000509756.1:n.*1379C>G
ENST00000689389.1:c.1525C>G (RAF1)	ENSP00000510213.1:p.Pro509Ala
ENST00000689418.1:c.*3597C>G (RAF1)	ENSP00000509467.1:n.*3597C>G
ENST00000689540.1:n.4070C>G (RAF1)
ENST00000689876.1:c.*251C>G (RAF1)	ENSP00000508535.1:n.*251C>G
ENST00000689914.1:c.*636C>G (RAF1)	ENSP00000509847.1:n.*636C>G
ENST00000690397.1:c.1591C>G (RAF1)	ENSP00000508730.1:p.Pro531Ala
ENST00000690460.1:c.1690C>G (RAF1)	ENSP00000509106.1:p.Pro564Ala
ENST00000690585.1:c.428C>G (RAF1)
ENST00000690625.1:n.2738C>G (RAF1)
ENST00000691396.1:c.*1574C>G (RAF1)	ENSP00000510712.1:n.*1574C>G
ENST00000691643.1:n.2755C>G (RAF1)
ENST00000691724.1:c.*659C>G (RAF1)	ENSP00000509255.1:n.*659C>G
ENST00000691779.1:c.*1280C>G (RAF1)	ENSP00000508592.1:n.*1280C>G
ENST00000691888.1:c.576C>G (RAF1)
ENST00000691899.1:c.1702C>G (RAF1)	ENSP00000508763.1:p.Pro568Ala
ENST00000692069.1:n.4626C>G (RAF1)
ENST00000692093.1:c.1603C>G (RAF1)	ENSP00000509669.1:p.Pro535Ala
ENST00000692311.1:n.2526C>G (RAF1)
ENST00000692558.1:n.4285C>G (RAF1)
ENST00000692773.1:c.*1439C>G (RAF1)	ENSP00000509055.1:n.*1439C>G
ENST00000692830.1:c.*1447C>G (RAF1)	ENSP00000509461.1:n.*1447C>G
ENST00000693312.1:c.1477C>G (RAF1)	ENSP00000508686.1:p.Pro493Ala
ENST00000693664.1:c.*153C>G (RAF1)	ENSP00000509614.1:n.*153C>G
ENST00000693705.1:c.*1081C>G (RAF1)	ENSP00000510697.1:n.*1081C>G
ENST00000251849.9:c.1702C>G (RAF1) MANE Select	ENSP00000251849.4:p.Pro568Ala
ENST00000442415.7:c.1762C>G (RAF1)	ENSP00000401888.2:p.Pro588Ala
ENST00000676541.1:c.*2695G>C (MKRN2)	ENSP00000503730.1:n.*2695G>C
ENST00000677142.1:c.*2695G>C (MKRN2)	ENSP00000504455.1:n.*2695G>C
ENST00000677816.1:c.*1250G>C (MKRN2)	ENSP00000502893.1:n.*1250G>C
ENST00000677941.1:n.2758G>C (MKRN2)
ENST00000251849.8:c.1702C>G (RAF1)	ENSP00000251849.4:p.Pro568Ala
ENST00000423275.5:c.*1379C>G (RAF1)	ENSP00000401088.1:n.*1379C>G
ENST00000432427.2:c.1339C>G (RAF1)	ENSP00000398591.2:p.Pro447Ala
ENST00000442415.6:c.1762C>G (RAF1)	ENSP00000401888.2:p.Pro588Ala
ENST00000471449.1:n.391C>G (RAF1)
NM_002880.3:c.1702C>G , LRG_413t1:c.1702C>G (RAF1)	NP_002871.1:p.Pro568Ala
XM_005265355.1:c.1702C>G (RAF1)	XP_005265412.1:p.Pro568Ala
XM_005265357.1:c.1603C>G (RAF1)	XP_005265414.1:p.Pro535Ala
XM_005265358.3:c.1459C>G (RAF1)	XP_005265415.1:p.Pro487Ala
XM_005265359.3:c.1360C>G (RAF1)	XP_005265416.1:p.Pro454Ala
XM_011533974.1:c.1702C>G (RAF1)	XP_011532276.1:p.Pro568Ala
XM_011533975.1:c.1459C>G (RAF1)	XP_011532277.1:p.Pro487Ala
NM_001354689.1:c.1762C>G (RAF1)	NP_001341618.1:p.Pro588Ala
NM_001354690.1:c.1702C>G (RAF1)	NP_001341619.1:p.Pro568Ala
NM_001354691.1:c.1459C>G (RAF1)	NP_001341620.1:p.Pro487Ala
NM_001354692.1:c.1459C>G (RAF1)	NP_001341621.1:p.Pro487Ala
NM_001354693.1:c.1603C>G (RAF1)	NP_001341622.1:p.Pro535Ala
NM_001354694.1:c.1519C>G (RAF1)	NP_001341623.1:p.Pro507Ala
NM_001354695.1:c.1360C>G (RAF1)	NP_001341624.1:p.Pro454Ala
NR_148940.1:n.2230C>G (RAF1)
NR_148941.1:n.2176C>G (RAF1)
NR_148942.1:n.2115C>G (RAF1)
XM_011533974.3:c.1702C>G (RAF1)	XP_011532276.1:p.Pro568Ala
XM_017006966.1:c.1603C>G (RAF1)	XP_016862455.1:p.Pro535Ala
NM_001354689.3:c.1762C>G (RAF1)	NP_001341618.1:p.Pro588Ala
NM_001354690.2:c.1702C>G (RAF1)	NP_001341619.1:p.Pro568Ala
NM_001354691.2:c.1459C>G (RAF1)	NP_001341620.1:p.Pro487Ala
NM_001354692.2:c.1459C>G (RAF1)	NP_001341621.1:p.Pro487Ala
NM_001354693.2:c.1603C>G (RAF1)	NP_001341622.1:p.Pro535Ala
NM_001354694.2:c.1519C>G (RAF1)	NP_001341623.1:p.Pro507Ala
NM_001354695.2:c.1360C>G (RAF1)	NP_001341624.1:p.Pro454Ala
NR_148940.2:n.2146C>G (RAF1)
NR_148941.2:n.2092C>G (RAF1)
NR_148942.2:n.2031C>G (RAF1)
NM_001354690.3:c.1702C>G (RAF1)	NP_001341619.1:p.Pro568Ala
NM_001354691.3:c.1459C>G (RAF1)	NP_001341620.1:p.Pro487Ala
NM_001354692.3:c.1459C>G (RAF1)	NP_001341621.1:p.Pro487Ala
NM_001354693.3:c.1603C>G (RAF1)	NP_001341622.1:p.Pro535Ala
NM_001354694.3:c.1519C>G (RAF1)	NP_001341623.1:p.Pro507Ala
NM_001354695.3:c.1360C>G (RAF1)	NP_001341624.1:p.Pro454Ala
NM_002880.4:c.1702C>G (RAF1) MANE Select	NP_002871.1:p.Pro568Ala
NR_148940.3:n.2146C>G (RAF1)
NR_148941.3:n.2092C>G (RAF1)
NR_148942.3:n.2031C>G (RAF1)