Canonical Allele Identifier: CA898402420

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs1446579332
• gnomAD v4: 3-12584492-C-G
• MyVariant Identifiers: chr3:g.12625991C>G (hg19) ; chr3:g.12584492C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584492C>G , CM000665.2:g.12584492C>G	GRCh38
NC_000003.11:g.12625991C>G , CM000665.1:g.12625991C>G	GRCh37
NC_000003.10:g.12600991C>G	NCBI36
NG_007467.1:g.84688G>C , LRG_413:g.84688G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1634G>C (RAF1)	ENSP00000401088.1:n.*1634G>C
ENST00000432427.3:c.1286G>C (RAF1)
ENST00000460610.2:n.6281G>C (RAF1)
ENST00000471449.2:n.779G>C (RAF1)
ENST00000475353.2:n.4249G>C (RAF1)
ENST00000684903.1:c.*1646G>C (RAF1)	ENSP00000508612.1:n.*1646G>C
ENST00000685348.1:c.*1680G>C (RAF1)	ENSP00000510285.1:n.*1680G>C
ENST00000685437.1:c.*22G>C (RAF1)	ENSP00000508794.1:n.*22G>C
ENST00000685653.1:c.*22G>C (RAF1)	ENSP00000509968.1:n.*22G>C
ENST00000685697.1:n.2704G>C (RAF1)
ENST00000685738.1:c.*933G>C (RAF1)	ENSP00000510156.1:n.*933G>C
ENST00000686409.1:n.5378G>C (RAF1)
ENST00000686455.1:n.4690G>C (RAF1)
ENST00000686762.1:c.*528G>C (RAF1)	ENSP00000509767.1:n.*528G>C
ENST00000687257.1:n.4423G>C (RAF1)
ENST00000687326.1:c.*3261G>C (RAF1)	ENSP00000509665.1:n.*3261G>C
ENST00000687505.1:n.2087G>C (RAF1)
ENST00000687923.1:c.*22G>C (RAF1)	ENSP00000510255.1:n.*22G>C
ENST00000688269.1:n.2565G>C (RAF1)
ENST00000688444.1:n.4086G>C (RAF1)
ENST00000688543.1:c.*22G>C (RAF1)	ENSP00000509612.1:n.*22G>C
ENST00000688625.1:c.*3338G>C (RAF1)	ENSP00000509522.1:n.*3338G>C
ENST00000688803.1:n.3397G>C (RAF1)
ENST00000689097.1:c.*1646G>C (RAF1)	ENSP00000509756.1:n.*1646G>C
ENST00000689389.1:c.*22G>C (RAF1)	ENSP00000510213.1:n.*22G>C
ENST00000689418.1:c.*3864G>C (RAF1)	ENSP00000509467.1:n.*3864G>C
ENST00000689540.1:n.4337G>C (RAF1)
ENST00000689876.1:c.*518G>C (RAF1)	ENSP00000508535.1:n.*518G>C
ENST00000689914.1:c.*903G>C (RAF1)	ENSP00000509847.1:n.*903G>C
ENST00000690397.1:c.*22G>C (RAF1)	ENSP00000508730.1:n.*22G>C
ENST00000690460.1:c.*22G>C (RAF1)	ENSP00000509106.1:n.*22G>C
ENST00000690585.1:c.695G>C (RAF1)
ENST00000690625.1:n.3005G>C (RAF1)
ENST00000691396.1:c.*1841G>C (RAF1)	ENSP00000510712.1:n.*1841G>C
ENST00000691643.1:n.3022G>C (RAF1)
ENST00000691724.1:c.*926G>C (RAF1)	ENSP00000509255.1:n.*926G>C
ENST00000691779.1:c.*1547G>C (RAF1)	ENSP00000508592.1:n.*1547G>C
ENST00000691888.1:c.843G>C (RAF1)
ENST00000691899.1:c.*22G>C (RAF1)	ENSP00000508763.1:n.*22G>C
ENST00000692069.1:n.4893G>C (RAF1)
ENST00000692093.1:c.*22G>C (RAF1)	ENSP00000509669.1:n.*22G>C
ENST00000692311.1:n.2793G>C (RAF1)
ENST00000692558.1:n.4552G>C (RAF1)
ENST00000692773.1:c.*1706G>C (RAF1)	ENSP00000509055.1:n.*1706G>C
ENST00000692830.1:c.*1714G>C (RAF1)	ENSP00000509461.1:n.*1714G>C
ENST00000693312.1:c.*22G>C (RAF1)	ENSP00000508686.1:n.*22G>C
ENST00000693664.1:c.*420G>C (RAF1)	ENSP00000509614.1:n.*420G>C
ENST00000693705.1:c.*1348G>C (RAF1)	ENSP00000510697.1:n.*1348G>C
ENST00000251849.9:c.*22G>C (RAF1) MANE Select	ENSP00000251849.4:n.*22G>C
ENST00000442415.7:c.*22G>C (RAF1)	ENSP00000401888.2:n.*22G>C
ENST00000676541.1:c.*2239C>G (MKRN2)	ENSP00000503730.1:n.*2239C>G
ENST00000677142.1:c.*2239C>G (MKRN2)	ENSP00000504455.1:n.*2239C>G
ENST00000677816.1:c.*794C>G (MKRN2)	ENSP00000502893.1:n.*794C>G
ENST00000677941.1:n.2302C>G (MKRN2)
ENST00000251849.8:c.*22G>C (RAF1)	ENSP00000251849.4:n.*22G>C
ENST00000423275.5:c.*1646G>C (RAF1)	ENSP00000401088.1:n.*1646G>C
ENST00000432427.2:c.1606G>C (RAF1)	ENSP00000398591.2:n.1606G>C
ENST00000442415.6:c.*22G>C (RAF1)	ENSP00000401888.2:n.*22G>C
ENST00000471449.1:n.658G>C (RAF1)
NM_002880.3:c.*22G>C , LRG_413t1:c.*22G>C (RAF1)	NP_002871.1:n.*22G>C
XM_005265355.1:c.*22G>C (RAF1)	XP_005265412.1:n.*22G>C
XM_005265357.1:c.*22G>C (RAF1)	XP_005265414.1:n.*22G>C
XM_005265358.3:c.*22G>C (RAF1)	XP_005265415.1:n.*22G>C
XM_005265359.3:c.*22G>C (RAF1)	XP_005265416.1:n.*22G>C
XM_011533974.1:c.*22G>C (RAF1)	XP_011532276.1:n.*22G>C
XM_011533975.1:c.*22G>C (RAF1)	XP_011532277.1:n.*22G>C
NM_001354689.1:c.*22G>C (RAF1)	NP_001341618.1:n.*22G>C
NM_001354690.1:c.*22G>C (RAF1)	NP_001341619.1:n.*22G>C
NM_001354691.1:c.*22G>C (RAF1)	NP_001341620.1:n.*22G>C
NM_001354692.1:c.*22G>C (RAF1)	NP_001341621.1:n.*22G>C
NM_001354693.1:c.*22G>C (RAF1)	NP_001341622.1:n.*22G>C
NM_001354694.1:c.*22G>C (RAF1)	NP_001341623.1:n.*22G>C
NM_001354695.1:c.*22G>C (RAF1)	NP_001341624.1:n.*22G>C
NR_148940.1:n.2497G>C (RAF1)
NR_148941.1:n.2443G>C (RAF1)
NR_148942.1:n.2382G>C (RAF1)
XM_011533974.3:c.*22G>C (RAF1)	XP_011532276.1:n.*22G>C
XM_017006966.1:c.*22G>C (RAF1)	XP_016862455.1:n.*22G>C
NM_001354689.3:c.*22G>C (RAF1)	NP_001341618.1:n.*22G>C
NM_001354690.2:c.*22G>C (RAF1)	NP_001341619.1:n.*22G>C
NM_001354691.2:c.*22G>C (RAF1)	NP_001341620.1:n.*22G>C
NM_001354692.2:c.*22G>C (RAF1)	NP_001341621.1:n.*22G>C
NM_001354693.2:c.*22G>C (RAF1)	NP_001341622.1:n.*22G>C
NM_001354694.2:c.*22G>C (RAF1)	NP_001341623.1:n.*22G>C
NM_001354695.2:c.*22G>C (RAF1)	NP_001341624.1:n.*22G>C
NR_148940.2:n.2413G>C (RAF1)
NR_148941.2:n.2359G>C (RAF1)
NR_148942.2:n.2298G>C (RAF1)
NM_001354690.3:c.*22G>C (RAF1)	NP_001341619.1:n.*22G>C
NM_001354691.3:c.*22G>C (RAF1)	NP_001341620.1:n.*22G>C
NM_001354692.3:c.*22G>C (RAF1)	NP_001341621.1:n.*22G>C
NM_001354693.3:c.*22G>C (RAF1)	NP_001341622.1:n.*22G>C
NM_001354694.3:c.*22G>C (RAF1)	NP_001341623.1:n.*22G>C
NM_001354695.3:c.*22G>C (RAF1)	NP_001341624.1:n.*22G>C
NM_002880.4:c.*22G>C (RAF1) MANE Select	NP_002871.1:n.*22G>C
NR_148940.3:n.2413G>C (RAF1)
NR_148941.3:n.2359G>C (RAF1)
NR_148942.3:n.2298G>C (RAF1)