Canonical Allele Identifier: CA351496715

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs2125319605
• MyVariant Identifiers: chr3:g.12626407A>C (hg19) ; chr3:g.12584908A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584908A>C , CM000665.2:g.12584908A>C	GRCh38
NC_000003.11:g.12626407A>C , CM000665.1:g.12626407A>C	GRCh37
NC_000003.10:g.12601407A>C	NCBI36
NG_007467.1:g.84272T>G , LRG_413:g.84272T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1407T>G (RAF1)	ENSP00000401088.1:n.*1407T>G
ENST00000432427.3:c.1059T>G (RAF1)
ENST00000460610.2:n.6054T>G (RAF1)
ENST00000471449.2:n.552T>G (RAF1)
ENST00000475353.2:n.4022T>G (RAF1)
ENST00000684903.1:c.*1419T>G (RAF1)	ENSP00000508612.1:n.*1419T>G
ENST00000685348.1:c.*1453T>G (RAF1)	ENSP00000510285.1:n.*1453T>G
ENST00000685437.1:c.1643T>G (RAF1)	ENSP00000508794.1:p.Met548Arg
ENST00000685653.1:c.1742T>G (RAF1)	ENSP00000509968.1:p.Met581Arg
ENST00000685697.1:n.2477T>G (RAF1)
ENST00000685738.1:c.*706T>G (RAF1)	ENSP00000510156.1:n.*706T>G
ENST00000686409.1:n.5151T>G (RAF1)
ENST00000686455.1:n.4463T>G (RAF1)
ENST00000686762.1:c.*301T>G (RAF1)	ENSP00000509767.1:n.*301T>G
ENST00000687257.1:n.4196T>G (RAF1)
ENST00000687326.1:c.*3034T>G (RAF1)	ENSP00000509665.1:n.*3034T>G
ENST00000687505.1:n.1860T>G (RAF1)
ENST00000687923.1:c.1631T>G (RAF1)	ENSP00000510255.1:p.Met544Arg
ENST00000688269.1:n.2338T>G (RAF1)
ENST00000688444.1:n.3859T>G (RAF1)
ENST00000688543.1:c.1643T>G (RAF1)	ENSP00000509612.1:p.Met548Arg
ENST00000688625.1:c.*3111T>G (RAF1)	ENSP00000509522.1:n.*3111T>G
ENST00000688803.1:n.3170T>G (RAF1)
ENST00000688914.1:n.1155T>G (RAF1)
ENST00000689097.1:c.*1419T>G (RAF1)	ENSP00000509756.1:n.*1419T>G
ENST00000689389.1:c.1565T>G (RAF1)	ENSP00000510213.1:p.Met522Arg
ENST00000689418.1:c.*3637T>G (RAF1)	ENSP00000509467.1:n.*3637T>G
ENST00000689540.1:n.4110T>G (RAF1)
ENST00000689876.1:c.*291T>G (RAF1)	ENSP00000508535.1:n.*291T>G
ENST00000689914.1:c.*676T>G (RAF1)	ENSP00000509847.1:n.*676T>G
ENST00000690397.1:c.1631T>G (RAF1)	ENSP00000508730.1:p.Met544Arg
ENST00000690460.1:c.1730T>G (RAF1)	ENSP00000509106.1:p.Met577Arg
ENST00000690585.1:c.468T>G (RAF1)
ENST00000690625.1:n.2778T>G (RAF1)
ENST00000691396.1:c.*1614T>G (RAF1)	ENSP00000510712.1:n.*1614T>G
ENST00000691643.1:n.2795T>G (RAF1)
ENST00000691724.1:c.*699T>G (RAF1)	ENSP00000509255.1:n.*699T>G
ENST00000691779.1:c.*1320T>G (RAF1)	ENSP00000508592.1:n.*1320T>G
ENST00000691888.1:c.616T>G (RAF1)
ENST00000691899.1:c.1742T>G (RAF1)	ENSP00000508763.1:p.Met581Arg
ENST00000692069.1:n.4666T>G (RAF1)
ENST00000692093.1:c.1643T>G (RAF1)	ENSP00000509669.1:p.Met548Arg
ENST00000692311.1:n.2566T>G (RAF1)
ENST00000692558.1:n.4325T>G (RAF1)
ENST00000692773.1:c.*1479T>G (RAF1)	ENSP00000509055.1:n.*1479T>G
ENST00000692830.1:c.*1487T>G (RAF1)	ENSP00000509461.1:n.*1487T>G
ENST00000693312.1:c.1517T>G (RAF1)	ENSP00000508686.1:p.Met506Arg
ENST00000693664.1:c.*193T>G (RAF1)	ENSP00000509614.1:n.*193T>G
ENST00000693705.1:c.*1121T>G (RAF1)	ENSP00000510697.1:n.*1121T>G
ENST00000251849.9:c.1742T>G (RAF1) MANE Select	ENSP00000251849.4:p.Met581Arg
ENST00000442415.7:c.1802T>G (RAF1)	ENSP00000401888.2:p.Met601Arg
ENST00000676541.1:c.*2655A>C (MKRN2)	ENSP00000503730.1:n.*2655A>C
ENST00000677142.1:c.*2655A>C (MKRN2)	ENSP00000504455.1:n.*2655A>C
ENST00000677816.1:c.*1210A>C (MKRN2)	ENSP00000502893.1:n.*1210A>C
ENST00000677941.1:n.2718A>C (MKRN2)
ENST00000251849.8:c.1742T>G (RAF1)	ENSP00000251849.4:p.Met581Arg
ENST00000423275.5:c.*1419T>G (RAF1)	ENSP00000401088.1:n.*1419T>G
ENST00000432427.2:c.1379T>G (RAF1)	ENSP00000398591.2:p.Met460Arg
ENST00000442415.6:c.1802T>G (RAF1)	ENSP00000401888.2:p.Met601Arg
ENST00000471449.1:n.431T>G (RAF1)
NM_002880.3:c.1742T>G , LRG_413t1:c.1742T>G (RAF1)	NP_002871.1:p.Met581Arg
XM_005265355.1:c.1742T>G (RAF1)	XP_005265412.1:p.Met581Arg
XM_005265357.1:c.1643T>G (RAF1)	XP_005265414.1:p.Met548Arg
XM_005265358.3:c.1499T>G (RAF1)	XP_005265415.1:p.Met500Arg
XM_005265359.3:c.1400T>G (RAF1)	XP_005265416.1:p.Met467Arg
XM_011533974.1:c.1742T>G (RAF1)	XP_011532276.1:p.Met581Arg
XM_011533975.1:c.1499T>G (RAF1)	XP_011532277.1:p.Met500Arg
NM_001354689.1:c.1802T>G (RAF1)	NP_001341618.1:p.Met601Arg
NM_001354690.1:c.1742T>G (RAF1)	NP_001341619.1:p.Met581Arg
NM_001354691.1:c.1499T>G (RAF1)	NP_001341620.1:p.Met500Arg
NM_001354692.1:c.1499T>G (RAF1)	NP_001341621.1:p.Met500Arg
NM_001354693.1:c.1643T>G (RAF1)	NP_001341622.1:p.Met548Arg
NM_001354694.1:c.1559T>G (RAF1)	NP_001341623.1:p.Met520Arg
NM_001354695.1:c.1400T>G (RAF1)	NP_001341624.1:p.Met467Arg
NR_148940.1:n.2270T>G (RAF1)
NR_148941.1:n.2216T>G (RAF1)
NR_148942.1:n.2155T>G (RAF1)
XM_011533974.3:c.1742T>G (RAF1)	XP_011532276.1:p.Met581Arg
XM_017006966.1:c.1643T>G (RAF1)	XP_016862455.1:p.Met548Arg
NM_001354689.3:c.1802T>G (RAF1)	NP_001341618.1:p.Met601Arg
NM_001354690.2:c.1742T>G (RAF1)	NP_001341619.1:p.Met581Arg
NM_001354691.2:c.1499T>G (RAF1)	NP_001341620.1:p.Met500Arg
NM_001354692.2:c.1499T>G (RAF1)	NP_001341621.1:p.Met500Arg
NM_001354693.2:c.1643T>G (RAF1)	NP_001341622.1:p.Met548Arg
NM_001354694.2:c.1559T>G (RAF1)	NP_001341623.1:p.Met520Arg
NM_001354695.2:c.1400T>G (RAF1)	NP_001341624.1:p.Met467Arg
NR_148940.2:n.2186T>G (RAF1)
NR_148941.2:n.2132T>G (RAF1)
NR_148942.2:n.2071T>G (RAF1)
NM_001354690.3:c.1742T>G (RAF1)	NP_001341619.1:p.Met581Arg
NM_001354691.3:c.1499T>G (RAF1)	NP_001341620.1:p.Met500Arg
NM_001354692.3:c.1499T>G (RAF1)	NP_001341621.1:p.Met500Arg
NM_001354693.3:c.1643T>G (RAF1)	NP_001341622.1:p.Met548Arg
NM_001354694.3:c.1559T>G (RAF1)	NP_001341623.1:p.Met520Arg
NM_001354695.3:c.1400T>G (RAF1)	NP_001341624.1:p.Met467Arg
NM_002880.4:c.1742T>G (RAF1) MANE Select	NP_002871.1:p.Met581Arg
NR_148940.3:n.2186T>G (RAF1)
NR_148941.3:n.2132T>G (RAF1)
NR_148942.3:n.2071T>G (RAF1)