Canonical Allele Identifier: CA2664506490

Gene: RAF1 MKRN2

Linked Data

• gnomAD v4: 3-12584252-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584252C>A , CM000665.2:g.12584252C>A	GRCh38
NC_000003.11:g.12625751C>A , CM000665.1:g.12625751C>A	GRCh37
NC_000003.10:g.12600751C>A	NCBI36
NG_007467.1:g.84928G>T , LRG_413:g.84928G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1874G>T (RAF1)	ENSP00000401088.1:n.*1874G>T
ENST00000432427.3:c.1526G>T (RAF1)
ENST00000460610.2:n.6521G>T (RAF1)
ENST00000471449.2:n.1019G>T (RAF1)
ENST00000475353.2:n.4489G>T (RAF1)
ENST00000684903.1:c.*1886G>T (RAF1)	ENSP00000508612.1:n.*1886G>T
ENST00000685348.1:c.*1920G>T (RAF1)	ENSP00000510285.1:n.*1920G>T
ENST00000685437.1:c.*262G>T (RAF1)	ENSP00000508794.1:n.*262G>T
ENST00000685653.1:c.*262G>T (RAF1)	ENSP00000509968.1:n.*262G>T
ENST00000685697.1:n.2944G>T (RAF1)
ENST00000685738.1:c.*1173G>T (RAF1)	ENSP00000510156.1:n.*1173G>T
ENST00000686409.1:n.5618G>T (RAF1)
ENST00000686455.1:n.4930G>T (RAF1)
ENST00000686762.1:c.*768G>T (RAF1)	ENSP00000509767.1:n.*768G>T
ENST00000687257.1:n.4663G>T (RAF1)
ENST00000687326.1:c.*3501G>T (RAF1)	ENSP00000509665.1:n.*3501G>T
ENST00000687505.1:n.2327G>T (RAF1)
ENST00000687923.1:c.*262G>T (RAF1)	ENSP00000510255.1:n.*262G>T
ENST00000688269.1:n.2805G>T (RAF1)
ENST00000688444.1:n.4326G>T (RAF1)
ENST00000688543.1:c.*262G>T (RAF1)	ENSP00000509612.1:n.*262G>T
ENST00000688625.1:c.*3578G>T (RAF1)	ENSP00000509522.1:n.*3578G>T
ENST00000688803.1:n.3637G>T (RAF1)
ENST00000689097.1:c.*1886G>T (RAF1)	ENSP00000509756.1:n.*1886G>T
ENST00000689389.1:c.*262G>T (RAF1)	ENSP00000510213.1:n.*262G>T
ENST00000689418.1:c.*4104G>T (RAF1)	ENSP00000509467.1:n.*4104G>T
ENST00000689540.1:n.4577G>T (RAF1)
ENST00000689876.1:c.*758G>T (RAF1)	ENSP00000508535.1:n.*758G>T
ENST00000689914.1:c.*1143G>T (RAF1)	ENSP00000509847.1:n.*1143G>T
ENST00000690397.1:c.*262G>T (RAF1)	ENSP00000508730.1:n.*262G>T
ENST00000690460.1:c.*262G>T (RAF1)	ENSP00000509106.1:n.*262G>T
ENST00000690585.1:c.935G>T (RAF1)
ENST00000690625.1:n.3245G>T (RAF1)
ENST00000691396.1:c.*2081G>T (RAF1)	ENSP00000510712.1:n.*2081G>T
ENST00000691643.1:n.3262G>T (RAF1)
ENST00000691724.1:c.*1166G>T (RAF1)	ENSP00000509255.1:n.*1166G>T
ENST00000691779.1:c.*1787G>T (RAF1)	ENSP00000508592.1:n.*1787G>T
ENST00000691888.1:c.1083G>T (RAF1)
ENST00000691899.1:c.*262G>T (RAF1)	ENSP00000508763.1:n.*262G>T
ENST00000692069.1:n.5133G>T (RAF1)
ENST00000692093.1:c.*262G>T (RAF1)	ENSP00000509669.1:n.*262G>T
ENST00000692311.1:n.3033G>T (RAF1)
ENST00000692558.1:n.4792G>T (RAF1)
ENST00000692773.1:c.*1946G>T (RAF1)	ENSP00000509055.1:n.*1946G>T
ENST00000692830.1:c.*1954G>T (RAF1)	ENSP00000509461.1:n.*1954G>T
ENST00000693312.1:c.*262G>T (RAF1)	ENSP00000508686.1:n.*262G>T
ENST00000693664.1:c.*660G>T (RAF1)	ENSP00000509614.1:n.*660G>T
ENST00000693705.1:c.*1588G>T (RAF1)	ENSP00000510697.1:n.*1588G>T
ENST00000251849.9:c.*262G>T (RAF1) MANE Select	ENSP00000251849.4:n.*262G>T
ENST00000442415.7:c.*262G>T (RAF1)	ENSP00000401888.2:n.*262G>T
ENST00000676541.1:c.*1999C>A (MKRN2)	ENSP00000503730.1:n.*1999C>A
ENST00000677142.1:c.*1999C>A (MKRN2)	ENSP00000504455.1:n.*1999C>A
ENST00000677816.1:c.*554C>A (MKRN2)	ENSP00000502893.1:n.*554C>A
ENST00000677941.1:n.2062C>A (MKRN2)
ENST00000251849.8:c.*262G>T (RAF1)	ENSP00000251849.4:n.*262G>T
ENST00000442415.6:c.*262G>T (RAF1)	ENSP00000401888.2:n.*262G>T
NM_002880.3:c.*262G>T , LRG_413t1:c.*262G>T (RAF1)	NP_002871.1:n.*262G>T
XM_005265355.1:c.*262G>T (RAF1)	XP_005265412.1:n.*262G>T
XM_005265357.1:c.*262G>T (RAF1)	XP_005265414.1:n.*262G>T
XM_005265358.3:c.*262G>T (RAF1)	XP_005265415.1:n.*262G>T
XM_005265359.3:c.*262G>T (RAF1)	XP_005265416.1:n.*262G>T
XM_011533974.1:c.*262G>T (RAF1)	XP_011532276.1:n.*262G>T
XM_011533975.1:c.*262G>T (RAF1)	XP_011532277.1:n.*262G>T
NM_001354689.1:c.*262G>T (RAF1)	NP_001341618.1:n.*262G>T
NM_001354690.1:c.*262G>T (RAF1)	NP_001341619.1:n.*262G>T
NM_001354691.1:c.*262G>T (RAF1)	NP_001341620.1:n.*262G>T
NM_001354692.1:c.*262G>T (RAF1)	NP_001341621.1:n.*262G>T
NM_001354693.1:c.*262G>T (RAF1)	NP_001341622.1:n.*262G>T
NM_001354694.1:c.*262G>T (RAF1)	NP_001341623.1:n.*262G>T
NM_001354695.1:c.*262G>T (RAF1)	NP_001341624.1:n.*262G>T
NR_148940.1:n.2737G>T (RAF1)
NR_148941.1:n.2683G>T (RAF1)
NR_148942.1:n.2622G>T (RAF1)
XM_011533974.3:c.*262G>T (RAF1)	XP_011532276.1:n.*262G>T
XM_017006966.1:c.*262G>T (RAF1)	XP_016862455.1:n.*262G>T
NM_001354689.3:c.*262G>T (RAF1)	NP_001341618.1:n.*262G>T
NM_001354690.2:c.*262G>T (RAF1)	NP_001341619.1:n.*262G>T
NM_001354691.2:c.*262G>T (RAF1)	NP_001341620.1:n.*262G>T
NM_001354692.2:c.*262G>T (RAF1)	NP_001341621.1:n.*262G>T
NM_001354693.2:c.*262G>T (RAF1)	NP_001341622.1:n.*262G>T
NM_001354694.2:c.*262G>T (RAF1)	NP_001341623.1:n.*262G>T
NM_001354695.2:c.*262G>T (RAF1)	NP_001341624.1:n.*262G>T
NR_148940.2:n.2653G>T (RAF1)
NR_148941.2:n.2599G>T (RAF1)
NR_148942.2:n.2538G>T (RAF1)
NM_001354690.3:c.*262G>T (RAF1)	NP_001341619.1:n.*262G>T
NM_001354691.3:c.*262G>T (RAF1)	NP_001341620.1:n.*262G>T
NM_001354692.3:c.*262G>T (RAF1)	NP_001341621.1:n.*262G>T
NM_001354693.3:c.*262G>T (RAF1)	NP_001341622.1:n.*262G>T
NM_001354694.3:c.*262G>T (RAF1)	NP_001341623.1:n.*262G>T
NM_001354695.3:c.*262G>T (RAF1)	NP_001341624.1:n.*262G>T
NM_002880.4:c.*262G>T (RAF1) MANE Select	NP_002871.1:n.*262G>T
NR_148940.3:n.2653G>T (RAF1)
NR_148941.3:n.2599G>T (RAF1)
NR_148942.3:n.2538G>T (RAF1)