Canonical Allele Identifier: CA2701951890

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs1038282942

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584437G>C , CM000665.2:g.12584437G>C	GRCh38
NC_000003.11:g.12625936G>C , CM000665.1:g.12625936G>C	GRCh37
NC_000003.10:g.12600936G>C	NCBI36
NG_007467.1:g.84743C>G , LRG_413:g.84743C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1689C>G (RAF1)	ENSP00000401088.1:n.*1689C>G
ENST00000432427.3:c.1341C>G (RAF1)
ENST00000460610.2:n.6336C>G (RAF1)
ENST00000471449.2:n.834C>G (RAF1)
ENST00000475353.2:n.4304C>G (RAF1)
ENST00000684903.1:c.*1701C>G (RAF1)	ENSP00000508612.1:n.*1701C>G
ENST00000685348.1:c.*1735C>G (RAF1)	ENSP00000510285.1:n.*1735C>G
ENST00000685437.1:c.*77C>G (RAF1)	ENSP00000508794.1:n.*77C>G
ENST00000685653.1:c.*77C>G (RAF1)	ENSP00000509968.1:n.*77C>G
ENST00000685697.1:n.2759C>G (RAF1)
ENST00000685738.1:c.*988C>G (RAF1)	ENSP00000510156.1:n.*988C>G
ENST00000686409.1:n.5433C>G (RAF1)
ENST00000686455.1:n.4745C>G (RAF1)
ENST00000686762.1:c.*583C>G (RAF1)	ENSP00000509767.1:n.*583C>G
ENST00000687257.1:n.4478C>G (RAF1)
ENST00000687326.1:c.*3316C>G (RAF1)	ENSP00000509665.1:n.*3316C>G
ENST00000687505.1:n.2142C>G (RAF1)
ENST00000687923.1:c.*77C>G (RAF1)	ENSP00000510255.1:n.*77C>G
ENST00000688269.1:n.2620C>G (RAF1)
ENST00000688444.1:n.4141C>G (RAF1)
ENST00000688543.1:c.*77C>G (RAF1)	ENSP00000509612.1:n.*77C>G
ENST00000688625.1:c.*3393C>G (RAF1)	ENSP00000509522.1:n.*3393C>G
ENST00000688803.1:n.3452C>G (RAF1)
ENST00000689097.1:c.*1701C>G (RAF1)	ENSP00000509756.1:n.*1701C>G
ENST00000689389.1:c.*77C>G (RAF1)	ENSP00000510213.1:n.*77C>G
ENST00000689418.1:c.*3919C>G (RAF1)	ENSP00000509467.1:n.*3919C>G
ENST00000689540.1:n.4392C>G (RAF1)
ENST00000689876.1:c.*573C>G (RAF1)	ENSP00000508535.1:n.*573C>G
ENST00000689914.1:c.*958C>G (RAF1)	ENSP00000509847.1:n.*958C>G
ENST00000690397.1:c.*77C>G (RAF1)	ENSP00000508730.1:n.*77C>G
ENST00000690460.1:c.*77C>G (RAF1)	ENSP00000509106.1:n.*77C>G
ENST00000690585.1:c.750C>G (RAF1)
ENST00000690625.1:n.3060C>G (RAF1)
ENST00000691396.1:c.*1896C>G (RAF1)	ENSP00000510712.1:n.*1896C>G
ENST00000691643.1:n.3077C>G (RAF1)
ENST00000691724.1:c.*981C>G (RAF1)	ENSP00000509255.1:n.*981C>G
ENST00000691779.1:c.*1602C>G (RAF1)	ENSP00000508592.1:n.*1602C>G
ENST00000691888.1:c.898C>G (RAF1)
ENST00000691899.1:c.*77C>G (RAF1)	ENSP00000508763.1:n.*77C>G
ENST00000692069.1:n.4948C>G (RAF1)
ENST00000692093.1:c.*77C>G (RAF1)	ENSP00000509669.1:n.*77C>G
ENST00000692311.1:n.2848C>G (RAF1)
ENST00000692558.1:n.4607C>G (RAF1)
ENST00000692773.1:c.*1761C>G (RAF1)	ENSP00000509055.1:n.*1761C>G
ENST00000692830.1:c.*1769C>G (RAF1)	ENSP00000509461.1:n.*1769C>G
ENST00000693312.1:c.*77C>G (RAF1)	ENSP00000508686.1:n.*77C>G
ENST00000693664.1:c.*475C>G (RAF1)	ENSP00000509614.1:n.*475C>G
ENST00000693705.1:c.*1403C>G (RAF1)	ENSP00000510697.1:n.*1403C>G
ENST00000251849.9:c.*77C>G (RAF1) MANE Select	ENSP00000251849.4:n.*77C>G
ENST00000442415.7:c.*77C>G (RAF1)	ENSP00000401888.2:n.*77C>G
ENST00000676541.1:c.*2184G>C (MKRN2)	ENSP00000503730.1:n.*2184G>C
ENST00000677142.1:c.*2184G>C (MKRN2)	ENSP00000504455.1:n.*2184G>C
ENST00000677816.1:c.*739G>C (MKRN2)	ENSP00000502893.1:n.*739G>C
ENST00000677941.1:n.2247G>C (MKRN2)
ENST00000251849.8:c.*77C>G (RAF1)	ENSP00000251849.4:n.*77C>G
ENST00000423275.5:c.*1701C>G (RAF1)	ENSP00000401088.1:n.*1701C>G
ENST00000432427.2:c.1661C>G (RAF1)	ENSP00000398591.2:n.1661C>G
ENST00000442415.6:c.*77C>G (RAF1)	ENSP00000401888.2:n.*77C>G
ENST00000471449.1:n.713C>G (RAF1)
NM_002880.3:c.*77C>G , LRG_413t1:c.*77C>G (RAF1)	NP_002871.1:n.*77C>G
XM_005265355.1:c.*77C>G (RAF1)	XP_005265412.1:n.*77C>G
XM_005265357.1:c.*77C>G (RAF1)	XP_005265414.1:n.*77C>G
XM_005265358.3:c.*77C>G (RAF1)	XP_005265415.1:n.*77C>G
XM_005265359.3:c.*77C>G (RAF1)	XP_005265416.1:n.*77C>G
XM_011533974.1:c.*77C>G (RAF1)	XP_011532276.1:n.*77C>G
XM_011533975.1:c.*77C>G (RAF1)	XP_011532277.1:n.*77C>G
NM_001354689.1:c.*77C>G (RAF1)	NP_001341618.1:n.*77C>G
NM_001354690.1:c.*77C>G (RAF1)	NP_001341619.1:n.*77C>G
NM_001354691.1:c.*77C>G (RAF1)	NP_001341620.1:n.*77C>G
NM_001354692.1:c.*77C>G (RAF1)	NP_001341621.1:n.*77C>G
NM_001354693.1:c.*77C>G (RAF1)	NP_001341622.1:n.*77C>G
NM_001354694.1:c.*77C>G (RAF1)	NP_001341623.1:n.*77C>G
NM_001354695.1:c.*77C>G (RAF1)	NP_001341624.1:n.*77C>G
NR_148940.1:n.2552C>G (RAF1)
NR_148941.1:n.2498C>G (RAF1)
NR_148942.1:n.2437C>G (RAF1)
XM_011533974.3:c.*77C>G (RAF1)	XP_011532276.1:n.*77C>G
XM_017006966.1:c.*77C>G (RAF1)	XP_016862455.1:n.*77C>G
NM_001354689.3:c.*77C>G (RAF1)	NP_001341618.1:n.*77C>G
NM_001354690.2:c.*77C>G (RAF1)	NP_001341619.1:n.*77C>G
NM_001354691.2:c.*77C>G (RAF1)	NP_001341620.1:n.*77C>G
NM_001354692.2:c.*77C>G (RAF1)	NP_001341621.1:n.*77C>G
NM_001354693.2:c.*77C>G (RAF1)	NP_001341622.1:n.*77C>G
NM_001354694.2:c.*77C>G (RAF1)	NP_001341623.1:n.*77C>G
NM_001354695.2:c.*77C>G (RAF1)	NP_001341624.1:n.*77C>G
NR_148940.2:n.2468C>G (RAF1)
NR_148941.2:n.2414C>G (RAF1)
NR_148942.2:n.2353C>G (RAF1)
NM_001354690.3:c.*77C>G (RAF1)	NP_001341619.1:n.*77C>G
NM_001354691.3:c.*77C>G (RAF1)	NP_001341620.1:n.*77C>G
NM_001354692.3:c.*77C>G (RAF1)	NP_001341621.1:n.*77C>G
NM_001354693.3:c.*77C>G (RAF1)	NP_001341622.1:n.*77C>G
NM_001354694.3:c.*77C>G (RAF1)	NP_001341623.1:n.*77C>G
NM_001354695.3:c.*77C>G (RAF1)	NP_001341624.1:n.*77C>G
NM_002880.4:c.*77C>G (RAF1) MANE Select	NP_002871.1:n.*77C>G
NR_148940.3:n.2468C>G (RAF1)
NR_148941.3:n.2414C>G (RAF1)
NR_148942.3:n.2353C>G (RAF1)