Canonical Allele Identifier: CA2664506631

Gene: RAF1 MKRN2

Linked Data

• gnomAD v4: 3-12584332-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584332C>T , CM000665.2:g.12584332C>T	GRCh38
NC_000003.11:g.12625831C>T , CM000665.1:g.12625831C>T	GRCh37
NC_000003.10:g.12600831C>T	NCBI36
NG_007467.1:g.84848G>A , LRG_413:g.84848G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1794G>A (RAF1)	ENSP00000401088.1:n.*1794G>A
ENST00000432427.3:c.1446G>A (RAF1)
ENST00000460610.2:n.6441G>A (RAF1)
ENST00000471449.2:n.939G>A (RAF1)
ENST00000475353.2:n.4409G>A (RAF1)
ENST00000684903.1:c.*1806G>A (RAF1)	ENSP00000508612.1:n.*1806G>A
ENST00000685348.1:c.*1840G>A (RAF1)	ENSP00000510285.1:n.*1840G>A
ENST00000685437.1:c.*182G>A (RAF1)	ENSP00000508794.1:n.*182G>A
ENST00000685653.1:c.*182G>A (RAF1)	ENSP00000509968.1:n.*182G>A
ENST00000685697.1:n.2864G>A (RAF1)
ENST00000685738.1:c.*1093G>A (RAF1)	ENSP00000510156.1:n.*1093G>A
ENST00000686409.1:n.5538G>A (RAF1)
ENST00000686455.1:n.4850G>A (RAF1)
ENST00000686762.1:c.*688G>A (RAF1)	ENSP00000509767.1:n.*688G>A
ENST00000687257.1:n.4583G>A (RAF1)
ENST00000687326.1:c.*3421G>A (RAF1)	ENSP00000509665.1:n.*3421G>A
ENST00000687505.1:n.2247G>A (RAF1)
ENST00000687923.1:c.*182G>A (RAF1)	ENSP00000510255.1:n.*182G>A
ENST00000688269.1:n.2725G>A (RAF1)
ENST00000688444.1:n.4246G>A (RAF1)
ENST00000688543.1:c.*182G>A (RAF1)	ENSP00000509612.1:n.*182G>A
ENST00000688625.1:c.*3498G>A (RAF1)	ENSP00000509522.1:n.*3498G>A
ENST00000688803.1:n.3557G>A (RAF1)
ENST00000689097.1:c.*1806G>A (RAF1)	ENSP00000509756.1:n.*1806G>A
ENST00000689389.1:c.*182G>A (RAF1)	ENSP00000510213.1:n.*182G>A
ENST00000689418.1:c.*4024G>A (RAF1)	ENSP00000509467.1:n.*4024G>A
ENST00000689540.1:n.4497G>A (RAF1)
ENST00000689876.1:c.*678G>A (RAF1)	ENSP00000508535.1:n.*678G>A
ENST00000689914.1:c.*1063G>A (RAF1)	ENSP00000509847.1:n.*1063G>A
ENST00000690397.1:c.*182G>A (RAF1)	ENSP00000508730.1:n.*182G>A
ENST00000690460.1:c.*182G>A (RAF1)	ENSP00000509106.1:n.*182G>A
ENST00000690585.1:c.855G>A (RAF1)
ENST00000690625.1:n.3165G>A (RAF1)
ENST00000691396.1:c.*2001G>A (RAF1)	ENSP00000510712.1:n.*2001G>A
ENST00000691643.1:n.3182G>A (RAF1)
ENST00000691724.1:c.*1086G>A (RAF1)	ENSP00000509255.1:n.*1086G>A
ENST00000691779.1:c.*1707G>A (RAF1)	ENSP00000508592.1:n.*1707G>A
ENST00000691888.1:c.1003G>A (RAF1)
ENST00000691899.1:c.*182G>A (RAF1)	ENSP00000508763.1:n.*182G>A
ENST00000692069.1:n.5053G>A (RAF1)
ENST00000692093.1:c.*182G>A (RAF1)	ENSP00000509669.1:n.*182G>A
ENST00000692311.1:n.2953G>A (RAF1)
ENST00000692558.1:n.4712G>A (RAF1)
ENST00000692773.1:c.*1866G>A (RAF1)	ENSP00000509055.1:n.*1866G>A
ENST00000692830.1:c.*1874G>A (RAF1)	ENSP00000509461.1:n.*1874G>A
ENST00000693312.1:c.*182G>A (RAF1)	ENSP00000508686.1:n.*182G>A
ENST00000693664.1:c.*580G>A (RAF1)	ENSP00000509614.1:n.*580G>A
ENST00000693705.1:c.*1508G>A (RAF1)	ENSP00000510697.1:n.*1508G>A
ENST00000251849.9:c.*182G>A (RAF1) MANE Select	ENSP00000251849.4:n.*182G>A
ENST00000442415.7:c.*182G>A (RAF1)	ENSP00000401888.2:n.*182G>A
ENST00000676541.1:c.*2079C>T (MKRN2)	ENSP00000503730.1:n.*2079C>T
ENST00000677142.1:c.*2079C>T (MKRN2)	ENSP00000504455.1:n.*2079C>T
ENST00000677816.1:c.*634C>T (MKRN2)	ENSP00000502893.1:n.*634C>T
ENST00000677941.1:n.2142C>T (MKRN2)
ENST00000251849.8:c.*182G>A (RAF1)	ENSP00000251849.4:n.*182G>A
ENST00000432427.2:c.1766G>A (RAF1)	ENSP00000398591.2:n.1766G>A
ENST00000442415.6:c.*182G>A (RAF1)	ENSP00000401888.2:n.*182G>A
NM_002880.3:c.*182G>A , LRG_413t1:c.*182G>A (RAF1)	NP_002871.1:n.*182G>A
XM_005265355.1:c.*182G>A (RAF1)	XP_005265412.1:n.*182G>A
XM_005265357.1:c.*182G>A (RAF1)	XP_005265414.1:n.*182G>A
XM_005265358.3:c.*182G>A (RAF1)	XP_005265415.1:n.*182G>A
XM_005265359.3:c.*182G>A (RAF1)	XP_005265416.1:n.*182G>A
XM_011533974.1:c.*182G>A (RAF1)	XP_011532276.1:n.*182G>A
XM_011533975.1:c.*182G>A (RAF1)	XP_011532277.1:n.*182G>A
NM_001354689.1:c.*182G>A (RAF1)	NP_001341618.1:n.*182G>A
NM_001354690.1:c.*182G>A (RAF1)	NP_001341619.1:n.*182G>A
NM_001354691.1:c.*182G>A (RAF1)	NP_001341620.1:n.*182G>A
NM_001354692.1:c.*182G>A (RAF1)	NP_001341621.1:n.*182G>A
NM_001354693.1:c.*182G>A (RAF1)	NP_001341622.1:n.*182G>A
NM_001354694.1:c.*182G>A (RAF1)	NP_001341623.1:n.*182G>A
NM_001354695.1:c.*182G>A (RAF1)	NP_001341624.1:n.*182G>A
NR_148940.1:n.2657G>A (RAF1)
NR_148941.1:n.2603G>A (RAF1)
NR_148942.1:n.2542G>A (RAF1)
XM_011533974.3:c.*182G>A (RAF1)	XP_011532276.1:n.*182G>A
XM_017006966.1:c.*182G>A (RAF1)	XP_016862455.1:n.*182G>A
NM_001354689.3:c.*182G>A (RAF1)	NP_001341618.1:n.*182G>A
NM_001354690.2:c.*182G>A (RAF1)	NP_001341619.1:n.*182G>A
NM_001354691.2:c.*182G>A (RAF1)	NP_001341620.1:n.*182G>A
NM_001354692.2:c.*182G>A (RAF1)	NP_001341621.1:n.*182G>A
NM_001354693.2:c.*182G>A (RAF1)	NP_001341622.1:n.*182G>A
NM_001354694.2:c.*182G>A (RAF1)	NP_001341623.1:n.*182G>A
NM_001354695.2:c.*182G>A (RAF1)	NP_001341624.1:n.*182G>A
NR_148940.2:n.2573G>A (RAF1)
NR_148941.2:n.2519G>A (RAF1)
NR_148942.2:n.2458G>A (RAF1)
NM_001354690.3:c.*182G>A (RAF1)	NP_001341619.1:n.*182G>A
NM_001354691.3:c.*182G>A (RAF1)	NP_001341620.1:n.*182G>A
NM_001354692.3:c.*182G>A (RAF1)	NP_001341621.1:n.*182G>A
NM_001354693.3:c.*182G>A (RAF1)	NP_001341622.1:n.*182G>A
NM_001354694.3:c.*182G>A (RAF1)	NP_001341623.1:n.*182G>A
NM_001354695.3:c.*182G>A (RAF1)	NP_001341624.1:n.*182G>A
NM_002880.4:c.*182G>A (RAF1) MANE Select	NP_002871.1:n.*182G>A
NR_148940.3:n.2573G>A (RAF1)
NR_148941.3:n.2519G>A (RAF1)
NR_148942.3:n.2458G>A (RAF1)