Canonical Allele Identifier: CA351501853

Gene: RAF1

Linked Data

• ClinVar Variation Id: 2450194
• ClinVar RCV Id: RCV003171354
• gnomAD v4: 3-12590844-T-C
• MyVariant Identifiers: chr3:g.12632343T>C (hg19) ; chr3:g.12590844T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590844T>C , CM000665.2:g.12590844T>C	GRCh38
NC_000003.11:g.12632343T>C , CM000665.1:g.12632343T>C	GRCh37
NC_000003.10:g.12607343T>C	NCBI36
NG_007467.1:g.78336A>G , LRG_413:g.78336A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*989A>G	ENSP00000401088.1:n.*989A>G
ENST00000432427.3:c.641A>G
ENST00000460610.2:n.118A>G
ENST00000465826.6:n.915A>G
ENST00000475353.2:n.1246A>G
ENST00000494557.2:n.1135A>G
ENST00000684903.1:c.*1001A>G	ENSP00000508612.1:n.*1001A>G
ENST00000685348.1:c.*1001A>G	ENSP00000510285.1:n.*1001A>G
ENST00000685437.1:c.1225A>G	ENSP00000508794.1:p.Met409Val
ENST00000685653.1:c.1324A>G	ENSP00000509968.1:p.Met442Val
ENST00000685738.1:c.*288A>G	ENSP00000510156.1:n.*288A>G
ENST00000686409.1:n.2375A>G
ENST00000686455.1:n.1687A>G
ENST00000686762.1:c.1324A>G	ENSP00000509767.1:p.Met442Val
ENST00000687257.1:n.1560A>G
ENST00000687326.1:c.*258A>G	ENSP00000509665.1:n.*258A>G
ENST00000687505.1:n.1442A>G
ENST00000687923.1:c.1213A>G	ENSP00000510255.1:p.Met405Val
ENST00000687940.1:n.1701A>G
ENST00000688269.1:n.1920A>G
ENST00000688326.1:c.757A>G
ENST00000688444.1:n.1650A>G
ENST00000688543.1:c.1225A>G	ENSP00000509612.1:p.Met409Val
ENST00000688625.1:c.*902A>G	ENSP00000509522.1:n.*902A>G
ENST00000688803.1:n.1555A>G
ENST00000688914.1:n.310A>G
ENST00000689097.1:c.*1001A>G	ENSP00000509756.1:n.*1001A>G
ENST00000689389.1:c.1193+864A>G	ENSP00000510213.1:n.1193+864A>G
ENST00000689418.1:c.*1001A>G	ENSP00000509467.1:n.*1001A>G
ENST00000689481.1:c.*1001A>G	ENSP00000510248.1:n.*1001A>G
ENST00000689540.1:n.1474A>G
ENST00000689876.1:c.1324A>G	ENSP00000508535.1:p.Met442Val
ENST00000689914.1:c.*258A>G	ENSP00000509847.1:n.*258A>G
ENST00000690397.1:c.1213A>G	ENSP00000508730.1:p.Met405Val
ENST00000690460.1:c.1312A>G	ENSP00000509106.1:p.Met438Val
ENST00000690585.1:c.216A>G
ENST00000690625.1:n.2360A>G
ENST00000691396.1:c.*1176A>G	ENSP00000510712.1:n.*1176A>G
ENST00000691724.1:c.*281A>G	ENSP00000509255.1:n.*281A>G
ENST00000691779.1:c.*902A>G	ENSP00000508592.1:n.*902A>G
ENST00000691888.1:c.216A>G
ENST00000691899.1:c.1324A>G	ENSP00000508763.1:p.Met442Val
ENST00000692069.1:n.1890A>G
ENST00000692093.1:c.1225A>G	ENSP00000509669.1:p.Met409Val
ENST00000692311.1:n.2148A>G
ENST00000692558.1:n.1689A>G
ENST00000692773.1:c.*1061A>G	ENSP00000509055.1:n.*1061A>G
ENST00000692830.1:c.*1069A>G	ENSP00000509461.1:n.*1069A>G
ENST00000693069.1:c.*258A>G	ENSP00000510072.1:n.*258A>G
ENST00000693312.1:c.1099A>G	ENSP00000508686.1:p.Met367Val
ENST00000693664.1:c.1324A>G	ENSP00000509614.1:p.Met442Val
ENST00000693705.1:c.*1001A>G	ENSP00000510697.1:n.*1001A>G
ENST00000251849.9:c.1324A>G MANE Select	ENSP00000251849.4:p.Met442Val
ENST00000442415.7:c.1384A>G	ENSP00000401888.2:p.Met462Val
ENST00000251849.8:c.1324A>G	ENSP00000251849.4:p.Met442Val
ENST00000423275.5:c.*1001A>G	ENSP00000401088.1:n.*1001A>G
ENST00000432427.2:c.961A>G	ENSP00000398591.2:p.Met321Val
ENST00000442415.6:c.1384A>G	ENSP00000401888.2:p.Met462Val
ENST00000460610.1:n.281A>G
ENST00000465826.5:n.681A>G
ENST00000475353.1:n.492A>G
ENST00000494557.1:n.340A>G
NM_002880.3:c.1324A>G , LRG_413t1:c.1324A>G	NP_002871.1:p.Met442Val
XM_005265355.1:c.1324A>G	XP_005265412.1:p.Met442Val
XM_005265357.1:c.1225A>G	XP_005265414.1:p.Met409Val
XM_005265358.3:c.1081A>G	XP_005265415.1:p.Met361Val
XM_005265359.3:c.982A>G	XP_005265416.1:p.Met328Val
XM_005265360.1:c.1324A>G	XP_005265417.1:p.Met442Val
XM_011533974.1:c.1324A>G	XP_011532276.1:p.Met442Val
XM_011533975.1:c.1081A>G	XP_011532277.1:p.Met361Val
NM_001354689.1:c.1384A>G	NP_001341618.1:p.Met462Val
NM_001354690.1:c.1324A>G	NP_001341619.1:p.Met442Val
NM_001354691.1:c.1081A>G	NP_001341620.1:p.Met361Val
NM_001354692.1:c.1081A>G	NP_001341621.1:p.Met361Val
NM_001354693.1:c.1225A>G	NP_001341622.1:p.Met409Val
NM_001354694.1:c.1141A>G	NP_001341623.1:p.Met381Val
NM_001354695.1:c.982A>G	NP_001341624.1:p.Met328Val
NR_148940.1:n.1852A>G
NR_148941.1:n.1798A>G
NR_148942.1:n.1737A>G
XM_011533974.3:c.1324A>G	XP_011532276.1:p.Met442Val
XM_017006966.1:c.1225A>G	XP_016862455.1:p.Met409Val
NM_001354689.3:c.1384A>G	NP_001341618.1:p.Met462Val
NM_001354690.2:c.1324A>G	NP_001341619.1:p.Met442Val
NM_001354691.2:c.1081A>G	NP_001341620.1:p.Met361Val
NM_001354692.2:c.1081A>G	NP_001341621.1:p.Met361Val
NM_001354693.2:c.1225A>G	NP_001341622.1:p.Met409Val
NM_001354694.2:c.1141A>G	NP_001341623.1:p.Met381Val
NM_001354695.2:c.982A>G	NP_001341624.1:p.Met328Val
NR_148940.2:n.1768A>G
NR_148941.2:n.1714A>G
NR_148942.2:n.1653A>G
NM_001354690.3:c.1324A>G	NP_001341619.1:p.Met442Val
NM_001354691.3:c.1081A>G	NP_001341620.1:p.Met361Val
NM_001354692.3:c.1081A>G	NP_001341621.1:p.Met361Val
NM_001354693.3:c.1225A>G	NP_001341622.1:p.Met409Val
NM_001354694.3:c.1141A>G	NP_001341623.1:p.Met381Val
NM_001354695.3:c.982A>G	NP_001341624.1:p.Met328Val
NM_002880.4:c.1324A>G MANE Select	NP_002871.1:p.Met442Val
NR_148940.3:n.1768A>G
NR_148941.3:n.1714A>G
NR_148942.3:n.1653A>G