Canonical Allele Identifier: CA2664506796

Gene: RAF1 MKRN2

Linked Data

• gnomAD v4: 3-12584447-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584447A>C , CM000665.2:g.12584447A>C	GRCh38
NC_000003.11:g.12625946A>C , CM000665.1:g.12625946A>C	GRCh37
NC_000003.10:g.12600946A>C	NCBI36
NG_007467.1:g.84733T>G , LRG_413:g.84733T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1679T>G (RAF1)	ENSP00000401088.1:n.*1679T>G
ENST00000432427.3:c.1331T>G (RAF1)
ENST00000460610.2:n.6326T>G (RAF1)
ENST00000471449.2:n.824T>G (RAF1)
ENST00000475353.2:n.4294T>G (RAF1)
ENST00000684903.1:c.*1691T>G (RAF1)	ENSP00000508612.1:n.*1691T>G
ENST00000685348.1:c.*1725T>G (RAF1)	ENSP00000510285.1:n.*1725T>G
ENST00000685437.1:c.*67T>G (RAF1)	ENSP00000508794.1:n.*67T>G
ENST00000685653.1:c.*67T>G (RAF1)	ENSP00000509968.1:n.*67T>G
ENST00000685697.1:n.2749T>G (RAF1)
ENST00000685738.1:c.*978T>G (RAF1)	ENSP00000510156.1:n.*978T>G
ENST00000686409.1:n.5423T>G (RAF1)
ENST00000686455.1:n.4735T>G (RAF1)
ENST00000686762.1:c.*573T>G (RAF1)	ENSP00000509767.1:n.*573T>G
ENST00000687257.1:n.4468T>G (RAF1)
ENST00000687326.1:c.*3306T>G (RAF1)	ENSP00000509665.1:n.*3306T>G
ENST00000687505.1:n.2132T>G (RAF1)
ENST00000687923.1:c.*67T>G (RAF1)	ENSP00000510255.1:n.*67T>G
ENST00000688269.1:n.2610T>G (RAF1)
ENST00000688444.1:n.4131T>G (RAF1)
ENST00000688543.1:c.*67T>G (RAF1)	ENSP00000509612.1:n.*67T>G
ENST00000688625.1:c.*3383T>G (RAF1)	ENSP00000509522.1:n.*3383T>G
ENST00000688803.1:n.3442T>G (RAF1)
ENST00000689097.1:c.*1691T>G (RAF1)	ENSP00000509756.1:n.*1691T>G
ENST00000689389.1:c.*67T>G (RAF1)	ENSP00000510213.1:n.*67T>G
ENST00000689418.1:c.*3909T>G (RAF1)	ENSP00000509467.1:n.*3909T>G
ENST00000689540.1:n.4382T>G (RAF1)
ENST00000689876.1:c.*563T>G (RAF1)	ENSP00000508535.1:n.*563T>G
ENST00000689914.1:c.*948T>G (RAF1)	ENSP00000509847.1:n.*948T>G
ENST00000690397.1:c.*67T>G (RAF1)	ENSP00000508730.1:n.*67T>G
ENST00000690460.1:c.*67T>G (RAF1)	ENSP00000509106.1:n.*67T>G
ENST00000690585.1:c.740T>G (RAF1)
ENST00000690625.1:n.3050T>G (RAF1)
ENST00000691396.1:c.*1886T>G (RAF1)	ENSP00000510712.1:n.*1886T>G
ENST00000691643.1:n.3067T>G (RAF1)
ENST00000691724.1:c.*971T>G (RAF1)	ENSP00000509255.1:n.*971T>G
ENST00000691779.1:c.*1592T>G (RAF1)	ENSP00000508592.1:n.*1592T>G
ENST00000691888.1:c.888T>G (RAF1)
ENST00000691899.1:c.*67T>G (RAF1)	ENSP00000508763.1:n.*67T>G
ENST00000692069.1:n.4938T>G (RAF1)
ENST00000692093.1:c.*67T>G (RAF1)	ENSP00000509669.1:n.*67T>G
ENST00000692311.1:n.2838T>G (RAF1)
ENST00000692558.1:n.4597T>G (RAF1)
ENST00000692773.1:c.*1751T>G (RAF1)	ENSP00000509055.1:n.*1751T>G
ENST00000692830.1:c.*1759T>G (RAF1)	ENSP00000509461.1:n.*1759T>G
ENST00000693312.1:c.*67T>G (RAF1)	ENSP00000508686.1:n.*67T>G
ENST00000693664.1:c.*465T>G (RAF1)	ENSP00000509614.1:n.*465T>G
ENST00000693705.1:c.*1393T>G (RAF1)	ENSP00000510697.1:n.*1393T>G
ENST00000251849.9:c.*67T>G (RAF1) MANE Select	ENSP00000251849.4:n.*67T>G
ENST00000442415.7:c.*67T>G (RAF1)	ENSP00000401888.2:n.*67T>G
ENST00000676541.1:c.*2194A>C (MKRN2)	ENSP00000503730.1:n.*2194A>C
ENST00000677142.1:c.*2194A>C (MKRN2)	ENSP00000504455.1:n.*2194A>C
ENST00000677816.1:c.*749A>C (MKRN2)	ENSP00000502893.1:n.*749A>C
ENST00000677941.1:n.2257A>C (MKRN2)
ENST00000251849.8:c.*67T>G (RAF1)	ENSP00000251849.4:n.*67T>G
ENST00000423275.5:c.*1691T>G (RAF1)	ENSP00000401088.1:n.*1691T>G
ENST00000432427.2:c.1651T>G (RAF1)	ENSP00000398591.2:n.1651T>G
ENST00000442415.6:c.*67T>G (RAF1)	ENSP00000401888.2:n.*67T>G
ENST00000471449.1:n.703T>G (RAF1)
NM_002880.3:c.*67T>G , LRG_413t1:c.*67T>G (RAF1)	NP_002871.1:n.*67T>G
XM_005265355.1:c.*67T>G (RAF1)	XP_005265412.1:n.*67T>G
XM_005265357.1:c.*67T>G (RAF1)	XP_005265414.1:n.*67T>G
XM_005265358.3:c.*67T>G (RAF1)	XP_005265415.1:n.*67T>G
XM_005265359.3:c.*67T>G (RAF1)	XP_005265416.1:n.*67T>G
XM_011533974.1:c.*67T>G (RAF1)	XP_011532276.1:n.*67T>G
XM_011533975.1:c.*67T>G (RAF1)	XP_011532277.1:n.*67T>G
NM_001354689.1:c.*67T>G (RAF1)	NP_001341618.1:n.*67T>G
NM_001354690.1:c.*67T>G (RAF1)	NP_001341619.1:n.*67T>G
NM_001354691.1:c.*67T>G (RAF1)	NP_001341620.1:n.*67T>G
NM_001354692.1:c.*67T>G (RAF1)	NP_001341621.1:n.*67T>G
NM_001354693.1:c.*67T>G (RAF1)	NP_001341622.1:n.*67T>G
NM_001354694.1:c.*67T>G (RAF1)	NP_001341623.1:n.*67T>G
NM_001354695.1:c.*67T>G (RAF1)	NP_001341624.1:n.*67T>G
NR_148940.1:n.2542T>G (RAF1)
NR_148941.1:n.2488T>G (RAF1)
NR_148942.1:n.2427T>G (RAF1)
XM_011533974.3:c.*67T>G (RAF1)	XP_011532276.1:n.*67T>G
XM_017006966.1:c.*67T>G (RAF1)	XP_016862455.1:n.*67T>G
NM_001354689.3:c.*67T>G (RAF1)	NP_001341618.1:n.*67T>G
NM_001354690.2:c.*67T>G (RAF1)	NP_001341619.1:n.*67T>G
NM_001354691.2:c.*67T>G (RAF1)	NP_001341620.1:n.*67T>G
NM_001354692.2:c.*67T>G (RAF1)	NP_001341621.1:n.*67T>G
NM_001354693.2:c.*67T>G (RAF1)	NP_001341622.1:n.*67T>G
NM_001354694.2:c.*67T>G (RAF1)	NP_001341623.1:n.*67T>G
NM_001354695.2:c.*67T>G (RAF1)	NP_001341624.1:n.*67T>G
NR_148940.2:n.2458T>G (RAF1)
NR_148941.2:n.2404T>G (RAF1)
NR_148942.2:n.2343T>G (RAF1)
NM_001354690.3:c.*67T>G (RAF1)	NP_001341619.1:n.*67T>G
NM_001354691.3:c.*67T>G (RAF1)	NP_001341620.1:n.*67T>G
NM_001354692.3:c.*67T>G (RAF1)	NP_001341621.1:n.*67T>G
NM_001354693.3:c.*67T>G (RAF1)	NP_001341622.1:n.*67T>G
NM_001354694.3:c.*67T>G (RAF1)	NP_001341623.1:n.*67T>G
NM_001354695.3:c.*67T>G (RAF1)	NP_001341624.1:n.*67T>G
NM_002880.4:c.*67T>G (RAF1) MANE Select	NP_002871.1:n.*67T>G
NR_148940.3:n.2458T>G (RAF1)
NR_148941.3:n.2404T>G (RAF1)
NR_148942.3:n.2343T>G (RAF1)