Canonical Allele Identifier: CA351497089

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626477T>C (hg19) ; chr3:g.12584978T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584978T>C , CM000665.2:g.12584978T>C	GRCh38
NC_000003.11:g.12626477T>C , CM000665.1:g.12626477T>C	GRCh37
NC_000003.10:g.12601477T>C	NCBI36
NG_007467.1:g.84202A>G , LRG_413:g.84202A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1337A>G (RAF1)	ENSP00000401088.1:n.*1337A>G
ENST00000432427.3:c.989A>G (RAF1)
ENST00000460610.2:n.5984A>G (RAF1)
ENST00000471449.2:n.482A>G (RAF1)
ENST00000475353.2:n.3952A>G (RAF1)
ENST00000684903.1:c.*1349A>G (RAF1)	ENSP00000508612.1:n.*1349A>G
ENST00000685348.1:c.*1383A>G (RAF1)	ENSP00000510285.1:n.*1383A>G
ENST00000685437.1:c.1573A>G (RAF1)	ENSP00000508794.1:p.Ile525Val
ENST00000685653.1:c.1672A>G (RAF1)	ENSP00000509968.1:p.Ile558Val
ENST00000685697.1:n.2407A>G (RAF1)
ENST00000685738.1:c.*636A>G (RAF1)	ENSP00000510156.1:n.*636A>G
ENST00000686409.1:n.5081A>G (RAF1)
ENST00000686455.1:n.4393A>G (RAF1)
ENST00000686762.1:c.*231A>G (RAF1)	ENSP00000509767.1:n.*231A>G
ENST00000687257.1:n.4126A>G (RAF1)
ENST00000687326.1:c.*2964A>G (RAF1)	ENSP00000509665.1:n.*2964A>G
ENST00000687505.1:n.1790A>G (RAF1)
ENST00000687923.1:c.1561A>G (RAF1)	ENSP00000510255.1:p.Ile521Val
ENST00000688269.1:n.2268A>G (RAF1)
ENST00000688444.1:n.3789A>G (RAF1)
ENST00000688543.1:c.1573A>G (RAF1)	ENSP00000509612.1:p.Ile525Val
ENST00000688625.1:c.*3041A>G (RAF1)	ENSP00000509522.1:n.*3041A>G
ENST00000688803.1:n.3100A>G (RAF1)
ENST00000688914.1:n.1085A>G (RAF1)
ENST00000689097.1:c.*1349A>G (RAF1)	ENSP00000509756.1:n.*1349A>G
ENST00000689389.1:c.1495A>G (RAF1)	ENSP00000510213.1:p.Ile499Val
ENST00000689418.1:c.*3567A>G (RAF1)	ENSP00000509467.1:n.*3567A>G
ENST00000689540.1:n.4040A>G (RAF1)
ENST00000689876.1:c.*221A>G (RAF1)	ENSP00000508535.1:n.*221A>G
ENST00000689914.1:c.*606A>G (RAF1)	ENSP00000509847.1:n.*606A>G
ENST00000690397.1:c.1561A>G (RAF1)	ENSP00000508730.1:p.Ile521Val
ENST00000690460.1:c.1660A>G (RAF1)	ENSP00000509106.1:p.Ile554Val
ENST00000690585.1:c.398A>G (RAF1)
ENST00000690625.1:n.2708A>G (RAF1)
ENST00000691396.1:c.*1544A>G (RAF1)	ENSP00000510712.1:n.*1544A>G
ENST00000691643.1:n.2725A>G (RAF1)
ENST00000691724.1:c.*629A>G (RAF1)	ENSP00000509255.1:n.*629A>G
ENST00000691779.1:c.*1250A>G (RAF1)	ENSP00000508592.1:n.*1250A>G
ENST00000691888.1:c.546A>G (RAF1)
ENST00000691899.1:c.1672A>G (RAF1)	ENSP00000508763.1:p.Ile558Val
ENST00000692069.1:n.4596A>G (RAF1)
ENST00000692093.1:c.1573A>G (RAF1)	ENSP00000509669.1:p.Ile525Val
ENST00000692311.1:n.2496A>G (RAF1)
ENST00000692558.1:n.4255A>G (RAF1)
ENST00000692773.1:c.*1409A>G (RAF1)	ENSP00000509055.1:n.*1409A>G
ENST00000692830.1:c.*1417A>G (RAF1)	ENSP00000509461.1:n.*1417A>G
ENST00000693312.1:c.1447A>G (RAF1)	ENSP00000508686.1:p.Ile483Val
ENST00000693664.1:c.*123A>G (RAF1)	ENSP00000509614.1:n.*123A>G
ENST00000693705.1:c.*1051A>G (RAF1)	ENSP00000510697.1:n.*1051A>G
ENST00000251849.9:c.1672A>G (RAF1) MANE Select	ENSP00000251849.4:p.Ile558Val
ENST00000442415.7:c.1732A>G (RAF1)	ENSP00000401888.2:p.Ile578Val
ENST00000676541.1:c.*2725T>C (MKRN2)	ENSP00000503730.1:n.*2725T>C
ENST00000677142.1:c.*2725T>C (MKRN2)	ENSP00000504455.1:n.*2725T>C
ENST00000677816.1:c.*1280T>C (MKRN2)	ENSP00000502893.1:n.*1280T>C
ENST00000677941.1:n.2788T>C (MKRN2)
ENST00000251849.8:c.1672A>G (RAF1)	ENSP00000251849.4:p.Ile558Val
ENST00000423275.5:c.*1349A>G (RAF1)	ENSP00000401088.1:n.*1349A>G
ENST00000432427.2:c.1309A>G (RAF1)	ENSP00000398591.2:p.Ile437Val
ENST00000442415.6:c.1732A>G (RAF1)	ENSP00000401888.2:p.Ile578Val
ENST00000471449.1:n.361A>G (RAF1)
NM_002880.3:c.1672A>G , LRG_413t1:c.1672A>G (RAF1)	NP_002871.1:p.Ile558Val
XM_005265355.1:c.1672A>G (RAF1)	XP_005265412.1:p.Ile558Val
XM_005265357.1:c.1573A>G (RAF1)	XP_005265414.1:p.Ile525Val
XM_005265358.3:c.1429A>G (RAF1)	XP_005265415.1:p.Ile477Val
XM_005265359.3:c.1330A>G (RAF1)	XP_005265416.1:p.Ile444Val
XM_011533974.1:c.1672A>G (RAF1)	XP_011532276.1:p.Ile558Val
XM_011533975.1:c.1429A>G (RAF1)	XP_011532277.1:p.Ile477Val
NM_001354689.1:c.1732A>G (RAF1)	NP_001341618.1:p.Ile578Val
NM_001354690.1:c.1672A>G (RAF1)	NP_001341619.1:p.Ile558Val
NM_001354691.1:c.1429A>G (RAF1)	NP_001341620.1:p.Ile477Val
NM_001354692.1:c.1429A>G (RAF1)	NP_001341621.1:p.Ile477Val
NM_001354693.1:c.1573A>G (RAF1)	NP_001341622.1:p.Ile525Val
NM_001354694.1:c.1489A>G (RAF1)	NP_001341623.1:p.Ile497Val
NM_001354695.1:c.1330A>G (RAF1)	NP_001341624.1:p.Ile444Val
NR_148940.1:n.2200A>G (RAF1)
NR_148941.1:n.2146A>G (RAF1)
NR_148942.1:n.2085A>G (RAF1)
XM_011533974.3:c.1672A>G (RAF1)	XP_011532276.1:p.Ile558Val
XM_017006966.1:c.1573A>G (RAF1)	XP_016862455.1:p.Ile525Val
NM_001354689.3:c.1732A>G (RAF1)	NP_001341618.1:p.Ile578Val
NM_001354690.2:c.1672A>G (RAF1)	NP_001341619.1:p.Ile558Val
NM_001354691.2:c.1429A>G (RAF1)	NP_001341620.1:p.Ile477Val
NM_001354692.2:c.1429A>G (RAF1)	NP_001341621.1:p.Ile477Val
NM_001354693.2:c.1573A>G (RAF1)	NP_001341622.1:p.Ile525Val
NM_001354694.2:c.1489A>G (RAF1)	NP_001341623.1:p.Ile497Val
NM_001354695.2:c.1330A>G (RAF1)	NP_001341624.1:p.Ile444Val
NR_148940.2:n.2116A>G (RAF1)
NR_148941.2:n.2062A>G (RAF1)
NR_148942.2:n.2001A>G (RAF1)
NM_001354690.3:c.1672A>G (RAF1)	NP_001341619.1:p.Ile558Val
NM_001354691.3:c.1429A>G (RAF1)	NP_001341620.1:p.Ile477Val
NM_001354692.3:c.1429A>G (RAF1)	NP_001341621.1:p.Ile477Val
NM_001354693.3:c.1573A>G (RAF1)	NP_001341622.1:p.Ile525Val
NM_001354694.3:c.1489A>G (RAF1)	NP_001341623.1:p.Ile497Val
NM_001354695.3:c.1330A>G (RAF1)	NP_001341624.1:p.Ile444Val
NM_002880.4:c.1672A>G (RAF1) MANE Select	NP_002871.1:p.Ile558Val
NR_148940.3:n.2116A>G (RAF1)
NR_148941.3:n.2062A>G (RAF1)
NR_148942.3:n.2001A>G (RAF1)