Canonical Allele Identifier: CA2664506629

Gene: RAF1 MKRN2

Linked Data

• gnomAD v4: 3-12584331-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584331C>T , CM000665.2:g.12584331C>T	GRCh38
NC_000003.11:g.12625830C>T , CM000665.1:g.12625830C>T	GRCh37
NC_000003.10:g.12600830C>T	NCBI36
NG_007467.1:g.84849G>A , LRG_413:g.84849G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1795G>A (RAF1)	ENSP00000401088.1:n.*1795G>A
ENST00000432427.3:c.1447G>A (RAF1)
ENST00000460610.2:n.6442G>A (RAF1)
ENST00000471449.2:n.940G>A (RAF1)
ENST00000475353.2:n.4410G>A (RAF1)
ENST00000684903.1:c.*1807G>A (RAF1)	ENSP00000508612.1:n.*1807G>A
ENST00000685348.1:c.*1841G>A (RAF1)	ENSP00000510285.1:n.*1841G>A
ENST00000685437.1:c.*183G>A (RAF1)	ENSP00000508794.1:n.*183G>A
ENST00000685653.1:c.*183G>A (RAF1)	ENSP00000509968.1:n.*183G>A
ENST00000685697.1:n.2865G>A (RAF1)
ENST00000685738.1:c.*1094G>A (RAF1)	ENSP00000510156.1:n.*1094G>A
ENST00000686409.1:n.5539G>A (RAF1)
ENST00000686455.1:n.4851G>A (RAF1)
ENST00000686762.1:c.*689G>A (RAF1)	ENSP00000509767.1:n.*689G>A
ENST00000687257.1:n.4584G>A (RAF1)
ENST00000687326.1:c.*3422G>A (RAF1)	ENSP00000509665.1:n.*3422G>A
ENST00000687505.1:n.2248G>A (RAF1)
ENST00000687923.1:c.*183G>A (RAF1)	ENSP00000510255.1:n.*183G>A
ENST00000688269.1:n.2726G>A (RAF1)
ENST00000688444.1:n.4247G>A (RAF1)
ENST00000688543.1:c.*183G>A (RAF1)	ENSP00000509612.1:n.*183G>A
ENST00000688625.1:c.*3499G>A (RAF1)	ENSP00000509522.1:n.*3499G>A
ENST00000688803.1:n.3558G>A (RAF1)
ENST00000689097.1:c.*1807G>A (RAF1)	ENSP00000509756.1:n.*1807G>A
ENST00000689389.1:c.*183G>A (RAF1)	ENSP00000510213.1:n.*183G>A
ENST00000689418.1:c.*4025G>A (RAF1)	ENSP00000509467.1:n.*4025G>A
ENST00000689540.1:n.4498G>A (RAF1)
ENST00000689876.1:c.*679G>A (RAF1)	ENSP00000508535.1:n.*679G>A
ENST00000689914.1:c.*1064G>A (RAF1)	ENSP00000509847.1:n.*1064G>A
ENST00000690397.1:c.*183G>A (RAF1)	ENSP00000508730.1:n.*183G>A
ENST00000690460.1:c.*183G>A (RAF1)	ENSP00000509106.1:n.*183G>A
ENST00000690585.1:c.856G>A (RAF1)
ENST00000690625.1:n.3166G>A (RAF1)
ENST00000691396.1:c.*2002G>A (RAF1)	ENSP00000510712.1:n.*2002G>A
ENST00000691643.1:n.3183G>A (RAF1)
ENST00000691724.1:c.*1087G>A (RAF1)	ENSP00000509255.1:n.*1087G>A
ENST00000691779.1:c.*1708G>A (RAF1)	ENSP00000508592.1:n.*1708G>A
ENST00000691888.1:c.1004G>A (RAF1)
ENST00000691899.1:c.*183G>A (RAF1)	ENSP00000508763.1:n.*183G>A
ENST00000692069.1:n.5054G>A (RAF1)
ENST00000692093.1:c.*183G>A (RAF1)	ENSP00000509669.1:n.*183G>A
ENST00000692311.1:n.2954G>A (RAF1)
ENST00000692558.1:n.4713G>A (RAF1)
ENST00000692773.1:c.*1867G>A (RAF1)	ENSP00000509055.1:n.*1867G>A
ENST00000692830.1:c.*1875G>A (RAF1)	ENSP00000509461.1:n.*1875G>A
ENST00000693312.1:c.*183G>A (RAF1)	ENSP00000508686.1:n.*183G>A
ENST00000693664.1:c.*581G>A (RAF1)	ENSP00000509614.1:n.*581G>A
ENST00000693705.1:c.*1509G>A (RAF1)	ENSP00000510697.1:n.*1509G>A
ENST00000251849.9:c.*183G>A (RAF1) MANE Select	ENSP00000251849.4:n.*183G>A
ENST00000442415.7:c.*183G>A (RAF1)	ENSP00000401888.2:n.*183G>A
ENST00000676541.1:c.*2078C>T (MKRN2)	ENSP00000503730.1:n.*2078C>T
ENST00000677142.1:c.*2078C>T (MKRN2)	ENSP00000504455.1:n.*2078C>T
ENST00000677816.1:c.*633C>T (MKRN2)	ENSP00000502893.1:n.*633C>T
ENST00000677941.1:n.2141C>T (MKRN2)
ENST00000251849.8:c.*183G>A (RAF1)	ENSP00000251849.4:n.*183G>A
ENST00000432427.2:c.1767G>A (RAF1)	ENSP00000398591.2:n.1767G>A
ENST00000442415.6:c.*183G>A (RAF1)	ENSP00000401888.2:n.*183G>A
NM_002880.3:c.*183G>A , LRG_413t1:c.*183G>A (RAF1)	NP_002871.1:n.*183G>A
XM_005265355.1:c.*183G>A (RAF1)	XP_005265412.1:n.*183G>A
XM_005265357.1:c.*183G>A (RAF1)	XP_005265414.1:n.*183G>A
XM_005265358.3:c.*183G>A (RAF1)	XP_005265415.1:n.*183G>A
XM_005265359.3:c.*183G>A (RAF1)	XP_005265416.1:n.*183G>A
XM_011533974.1:c.*183G>A (RAF1)	XP_011532276.1:n.*183G>A
XM_011533975.1:c.*183G>A (RAF1)	XP_011532277.1:n.*183G>A
NM_001354689.1:c.*183G>A (RAF1)	NP_001341618.1:n.*183G>A
NM_001354690.1:c.*183G>A (RAF1)	NP_001341619.1:n.*183G>A
NM_001354691.1:c.*183G>A (RAF1)	NP_001341620.1:n.*183G>A
NM_001354692.1:c.*183G>A (RAF1)	NP_001341621.1:n.*183G>A
NM_001354693.1:c.*183G>A (RAF1)	NP_001341622.1:n.*183G>A
NM_001354694.1:c.*183G>A (RAF1)	NP_001341623.1:n.*183G>A
NM_001354695.1:c.*183G>A (RAF1)	NP_001341624.1:n.*183G>A
NR_148940.1:n.2658G>A (RAF1)
NR_148941.1:n.2604G>A (RAF1)
NR_148942.1:n.2543G>A (RAF1)
XM_011533974.3:c.*183G>A (RAF1)	XP_011532276.1:n.*183G>A
XM_017006966.1:c.*183G>A (RAF1)	XP_016862455.1:n.*183G>A
NM_001354689.3:c.*183G>A (RAF1)	NP_001341618.1:n.*183G>A
NM_001354690.2:c.*183G>A (RAF1)	NP_001341619.1:n.*183G>A
NM_001354691.2:c.*183G>A (RAF1)	NP_001341620.1:n.*183G>A
NM_001354692.2:c.*183G>A (RAF1)	NP_001341621.1:n.*183G>A
NM_001354693.2:c.*183G>A (RAF1)	NP_001341622.1:n.*183G>A
NM_001354694.2:c.*183G>A (RAF1)	NP_001341623.1:n.*183G>A
NM_001354695.2:c.*183G>A (RAF1)	NP_001341624.1:n.*183G>A
NR_148940.2:n.2574G>A (RAF1)
NR_148941.2:n.2520G>A (RAF1)
NR_148942.2:n.2459G>A (RAF1)
NM_001354690.3:c.*183G>A (RAF1)	NP_001341619.1:n.*183G>A
NM_001354691.3:c.*183G>A (RAF1)	NP_001341620.1:n.*183G>A
NM_001354692.3:c.*183G>A (RAF1)	NP_001341621.1:n.*183G>A
NM_001354693.3:c.*183G>A (RAF1)	NP_001341622.1:n.*183G>A
NM_001354694.3:c.*183G>A (RAF1)	NP_001341623.1:n.*183G>A
NM_001354695.3:c.*183G>A (RAF1)	NP_001341624.1:n.*183G>A
NM_002880.4:c.*183G>A (RAF1) MANE Select	NP_002871.1:n.*183G>A
NR_148940.3:n.2574G>A (RAF1)
NR_148941.3:n.2520G>A (RAF1)
NR_148942.3:n.2459G>A (RAF1)