Canonical Allele Identifier: CA2664506514

Gene: RAF1 MKRN2

Linked Data

• gnomAD v4: 3-12584263-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584266del , CM000665.2:g.12584266del	GRCh38
NC_000003.11:g.12625765del , CM000665.1:g.12625765del	GRCh37
NC_000003.10:g.12600765del	NCBI36
NG_007467.1:g.84916del , LRG_413:g.84916del

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1862del (RAF1)	ENSP00000401088.1:n.*1862del
ENST00000432427.3:c.1514del (RAF1)
ENST00000460610.2:n.6509del (RAF1)
ENST00000471449.2:n.1007del (RAF1)
ENST00000475353.2:n.4477del (RAF1)
ENST00000684903.1:c.*1874del (RAF1)	ENSP00000508612.1:n.*1874del
ENST00000685348.1:c.*1908del (RAF1)	ENSP00000510285.1:n.*1908del
ENST00000685437.1:c.*250del (RAF1)	ENSP00000508794.1:n.*250del
ENST00000685653.1:c.*250del (RAF1)	ENSP00000509968.1:n.*250del
ENST00000685697.1:n.2932del (RAF1)
ENST00000685738.1:c.*1161del (RAF1)	ENSP00000510156.1:n.*1161del
ENST00000686409.1:n.5606del (RAF1)
ENST00000686455.1:n.4918del (RAF1)
ENST00000686762.1:c.*756del (RAF1)	ENSP00000509767.1:n.*756del
ENST00000687257.1:n.4651del (RAF1)
ENST00000687326.1:c.*3489del (RAF1)	ENSP00000509665.1:n.*3489del
ENST00000687505.1:n.2315del (RAF1)
ENST00000687923.1:c.*250del (RAF1)	ENSP00000510255.1:n.*250del
ENST00000688269.1:n.2793del (RAF1)
ENST00000688444.1:n.4314del (RAF1)
ENST00000688543.1:c.*250del (RAF1)	ENSP00000509612.1:n.*250del
ENST00000688625.1:c.*3566del (RAF1)	ENSP00000509522.1:n.*3566del
ENST00000688803.1:n.3625del (RAF1)
ENST00000689097.1:c.*1874del (RAF1)	ENSP00000509756.1:n.*1874del
ENST00000689389.1:c.*250del (RAF1)	ENSP00000510213.1:n.*250del
ENST00000689418.1:c.*4092del (RAF1)	ENSP00000509467.1:n.*4092del
ENST00000689540.1:n.4565del (RAF1)
ENST00000689876.1:c.*746del (RAF1)	ENSP00000508535.1:n.*746del
ENST00000689914.1:c.*1131del (RAF1)	ENSP00000509847.1:n.*1131del
ENST00000690397.1:c.*250del (RAF1)	ENSP00000508730.1:n.*250del
ENST00000690460.1:c.*250del (RAF1)	ENSP00000509106.1:n.*250del
ENST00000690585.1:c.923del (RAF1)
ENST00000690625.1:n.3233del (RAF1)
ENST00000691396.1:c.*2069del (RAF1)	ENSP00000510712.1:n.*2069del
ENST00000691643.1:n.3250del (RAF1)
ENST00000691724.1:c.*1154del (RAF1)	ENSP00000509255.1:n.*1154del
ENST00000691779.1:c.*1775del (RAF1)	ENSP00000508592.1:n.*1775del
ENST00000691888.1:c.1071del (RAF1)
ENST00000691899.1:c.*250del (RAF1)	ENSP00000508763.1:n.*250del
ENST00000692069.1:n.5121del (RAF1)
ENST00000692093.1:c.*250del (RAF1)	ENSP00000509669.1:n.*250del
ENST00000692311.1:n.3021del (RAF1)
ENST00000692558.1:n.4780del (RAF1)
ENST00000692773.1:c.*1934del (RAF1)	ENSP00000509055.1:n.*1934del
ENST00000692830.1:c.*1942del (RAF1)	ENSP00000509461.1:n.*1942del
ENST00000693312.1:c.*250del (RAF1)	ENSP00000508686.1:n.*250del
ENST00000693664.1:c.*648del (RAF1)	ENSP00000509614.1:n.*648del
ENST00000693705.1:c.*1576del (RAF1)	ENSP00000510697.1:n.*1576del
ENST00000251849.9:c.*250del (RAF1) MANE Select	ENSP00000251849.4:n.*250del
ENST00000442415.7:c.*250del (RAF1)	ENSP00000401888.2:n.*250del
ENST00000676541.1:c.*2013del (MKRN2)	ENSP00000503730.1:n.*2013del
ENST00000677142.1:c.*2013del (MKRN2)	ENSP00000504455.1:n.*2013del
ENST00000677816.1:c.*568del (MKRN2)	ENSP00000502893.1:n.*568del
ENST00000677941.1:n.2076del (MKRN2)
ENST00000251849.8:c.*250del (RAF1)	ENSP00000251849.4:n.*250del
ENST00000442415.6:c.*250del (RAF1)	ENSP00000401888.2:n.*250del
NM_002880.3:c.*250del , LRG_413t1:c.*250del (RAF1)	NP_002871.1:n.*250del
XM_005265355.1:c.*250del (RAF1)	XP_005265412.1:n.*250del
XM_005265357.1:c.*250del (RAF1)	XP_005265414.1:n.*250del
XM_005265358.3:c.*250del (RAF1)	XP_005265415.1:n.*250del
XM_005265359.3:c.*250del (RAF1)	XP_005265416.1:n.*250del
XM_011533974.1:c.*250del (RAF1)	XP_011532276.1:n.*250del
XM_011533975.1:c.*250del (RAF1)	XP_011532277.1:n.*250del
NM_001354689.1:c.*250del (RAF1)	NP_001341618.1:n.*250del
NM_001354690.1:c.*250del (RAF1)	NP_001341619.1:n.*250del
NM_001354691.1:c.*250del (RAF1)	NP_001341620.1:n.*250del
NM_001354692.1:c.*250del (RAF1)	NP_001341621.1:n.*250del
NM_001354693.1:c.*250del (RAF1)	NP_001341622.1:n.*250del
NM_001354694.1:c.*250del (RAF1)	NP_001341623.1:n.*250del
NM_001354695.1:c.*250del (RAF1)	NP_001341624.1:n.*250del
NR_148940.1:n.2725del (RAF1)
NR_148941.1:n.2671del (RAF1)
NR_148942.1:n.2610del (RAF1)
XM_011533974.3:c.*250del (RAF1)	XP_011532276.1:n.*250del
XM_017006966.1:c.*250del (RAF1)	XP_016862455.1:n.*250del
NM_001354689.3:c.*250del (RAF1)	NP_001341618.1:n.*250del
NM_001354690.2:c.*250del (RAF1)	NP_001341619.1:n.*250del
NM_001354691.2:c.*250del (RAF1)	NP_001341620.1:n.*250del
NM_001354692.2:c.*250del (RAF1)	NP_001341621.1:n.*250del
NM_001354693.2:c.*250del (RAF1)	NP_001341622.1:n.*250del
NM_001354694.2:c.*250del (RAF1)	NP_001341623.1:n.*250del
NM_001354695.2:c.*250del (RAF1)	NP_001341624.1:n.*250del
NR_148940.2:n.2641del (RAF1)
NR_148941.2:n.2587del (RAF1)
NR_148942.2:n.2526del (RAF1)
NM_001354690.3:c.*250del (RAF1)	NP_001341619.1:n.*250del
NM_001354691.3:c.*250del (RAF1)	NP_001341620.1:n.*250del
NM_001354692.3:c.*250del (RAF1)	NP_001341621.1:n.*250del
NM_001354693.3:c.*250del (RAF1)	NP_001341622.1:n.*250del
NM_001354694.3:c.*250del (RAF1)	NP_001341623.1:n.*250del
NM_001354695.3:c.*250del (RAF1)	NP_001341624.1:n.*250del
NM_002880.4:c.*250del (RAF1) MANE Select	NP_002871.1:n.*250del
NR_148940.3:n.2641del (RAF1)
NR_148941.3:n.2587del (RAF1)
NR_148942.3:n.2526del (RAF1)