Canonical Allele Identifier: CA2664504584

Gene: RAF1

Linked Data

• gnomAD v4: 3-12599613-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12599614del , CM000665.2:g.12599614del	GRCh38
NC_000003.11:g.12641113del , CM000665.1:g.12641113del	GRCh37
NC_000003.10:g.12616113del	NCBI36
NG_007467.1:g.69566del , LRG_413:g.69566del

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*773+77del	ENSP00000401088.1:n.*773+77del
ENST00000432427.3:c.428+77del
ENST00000465826.6:n.699+77del
ENST00000491290.2:n.1485+77del
ENST00000684903.1:c.*785+77del	ENSP00000508612.1:n.*785+77del
ENST00000685348.1:c.*785+77del	ENSP00000510285.1:n.*785+77del
ENST00000685437.1:c.1009+77del	ENSP00000508794.1:n.1009+77del
ENST00000685653.1:c.1108+77del	ENSP00000509968.1:n.1108+77del
ENST00000685738.1:c.1108+77del	ENSP00000510156.1:n.1108+77del
ENST00000686409.1:n.2159+77del
ENST00000686455.1:n.1471+77del
ENST00000686479.1:n.1556del
ENST00000686762.1:c.1108+77del	ENSP00000509767.1:n.1108+77del
ENST00000687257.1:n.1344+77del
ENST00000687326.1:c.1108+77del	ENSP00000509665.1:n.1108+77del
ENST00000687486.1:c.300+77del
ENST00000687505.1:n.1226+77del
ENST00000687923.1:c.997+89del	ENSP00000510255.1:n.997+89del
ENST00000687940.1:n.1485+77del
ENST00000688269.1:n.1704+77del
ENST00000688326.1:c.428+77del
ENST00000688444.1:n.1434+77del
ENST00000688543.1:c.1009+77del	ENSP00000509612.1:n.1009+77del
ENST00000688625.1:c.*686+77del	ENSP00000509522.1:n.*686+77del
ENST00000688803.1:n.1339+77del
ENST00000688914.1:n.94+77del
ENST00000689097.1:c.*785+77del	ENSP00000509756.1:n.*785+77del
ENST00000689389.1:c.1108+77del	ENSP00000510213.1:n.1108+77del
ENST00000689418.1:c.*785+77del	ENSP00000509467.1:n.*785+77del
ENST00000689481.1:c.*785+77del	ENSP00000510248.1:n.*785+77del
ENST00000689540.1:n.1258+77del
ENST00000689876.1:c.1108+77del	ENSP00000508535.1:n.1108+77del
ENST00000689914.1:c.1108+77del	ENSP00000509847.1:n.1108+77del
ENST00000690397.1:c.997+77del	ENSP00000508730.1:n.997+77del
ENST00000690460.1:c.1096+77del	ENSP00000509106.1:n.1096+77del
ENST00000690625.1:n.1411+77del
ENST00000691396.1:c.*901+77del	ENSP00000510712.1:n.*901+77del
ENST00000691724.1:c.*65+77del	ENSP00000509255.1:n.*65+77del
ENST00000691779.1:c.*686+77del	ENSP00000508592.1:n.*686+77del
ENST00000691899.1:c.1108+77del	ENSP00000508763.1:n.1108+77del
ENST00000692069.1:n.1674+77del
ENST00000692093.1:c.1009+77del	ENSP00000509669.1:n.1009+77del
ENST00000692311.1:n.1932+77del
ENST00000692558.1:n.1473+77del
ENST00000692773.1:c.*845+77del	ENSP00000509055.1:n.*845+77del
ENST00000692830.1:c.*853+77del	ENSP00000509461.1:n.*853+77del
ENST00000693069.1:c.1009+77del	ENSP00000510072.1:n.1009+77del
ENST00000693312.1:c.883+77del	ENSP00000508686.1:n.883+77del
ENST00000693664.1:c.1108+77del	ENSP00000509614.1:n.1108+77del
ENST00000693705.1:c.*785+77del	ENSP00000510697.1:n.*785+77del
ENST00000251849.9:c.1108+77del MANE Select	ENSP00000251849.4:n.1108+77del
ENST00000442415.7:c.1168+77del	ENSP00000401888.2:n.1168+77del
ENST00000251849.8:c.1108+77del	ENSP00000251849.4:n.1108+77del
ENST00000423275.5:c.*785+77del	ENSP00000401088.1:n.*785+77del
ENST00000432427.2:c.745+77del	ENSP00000398591.2:n.745+77del
ENST00000442415.6:c.1168+77del	ENSP00000401888.2:n.1168+77del
ENST00000460610.1:n.65+77del
ENST00000465826.5:n.352+77del
NM_002880.3:c.1108+77del , LRG_413t1:c.1108+77del	NP_002871.1:n.1108+77del
XM_005265355.1:c.1108+77del	XP_005265412.1:n.1108+77del
XM_005265357.1:c.1009+77del	XP_005265414.1:n.1009+77del
XM_005265358.3:c.865+77del	XP_005265415.1:n.865+77del
XM_005265359.3:c.766+77del	XP_005265416.1:n.766+77del
XM_005265360.1:c.1108+77del	XP_005265417.1:n.1108+77del
XM_011533974.1:c.1108+77del	XP_011532276.1:n.1108+77del
XM_011533975.1:c.865+77del	XP_011532277.1:n.865+77del
NM_001354689.1:c.1168+77del	NP_001341618.1:n.1168+77del
NM_001354690.1:c.1108+77del	NP_001341619.1:n.1108+77del
NM_001354691.1:c.865+77del	NP_001341620.1:n.865+77del
NM_001354692.1:c.865+77del	NP_001341621.1:n.865+77del
NM_001354693.1:c.1009+77del	NP_001341622.1:n.1009+77del
NM_001354694.1:c.925+77del	NP_001341623.1:n.925+77del
NM_001354695.1:c.766+77del	NP_001341624.1:n.766+77del
NR_148940.1:n.1523+77del
NR_148941.1:n.1523+77del
NR_148942.1:n.1521+77del
XM_011533974.3:c.1108+77del	XP_011532276.1:n.1108+77del
XM_017006966.1:c.1009+77del	XP_016862455.1:n.1009+77del
XR_001740227.1:n.1340+77del
NM_001354689.3:c.1168+77del	NP_001341618.1:n.1168+77del
NM_001354690.2:c.1108+77del	NP_001341619.1:n.1108+77del
NM_001354691.2:c.865+77del	NP_001341620.1:n.865+77del
NM_001354692.2:c.865+77del	NP_001341621.1:n.865+77del
NM_001354693.2:c.1009+77del	NP_001341622.1:n.1009+77del
NM_001354694.2:c.925+77del	NP_001341623.1:n.925+77del
NM_001354695.2:c.766+77del	NP_001341624.1:n.766+77del
NR_148940.2:n.1439+77del
NR_148941.2:n.1439+77del
NR_148942.2:n.1437+77del
NM_001354690.3:c.1108+77del	NP_001341619.1:n.1108+77del
NM_001354691.3:c.865+77del	NP_001341620.1:n.865+77del
NM_001354692.3:c.865+77del	NP_001341621.1:n.865+77del
NM_001354693.3:c.1009+77del	NP_001341622.1:n.1009+77del
NM_001354694.3:c.925+77del	NP_001341623.1:n.925+77del
NM_001354695.3:c.766+77del	NP_001341624.1:n.766+77del
NM_002880.4:c.1108+77del MANE Select	NP_002871.1:n.1108+77del
NR_148940.3:n.1439+77del
NR_148941.3:n.1439+77del
NR_148942.3:n.1437+77del