Canonical Allele Identifier: CA2664507089

Linked Data

gnomAD v4: 3-12585583-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12585583G>C , CM000665.2:g.12585583G>C GRCh38
NC_000003.11:g.12627082G>C , CM000665.1:g.12627082G>C GRCh37
NC_000003.10:g.12602082G>C NCBI36
NG_007467.1:g.83597C>G , LRG_413:g.83597C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1201+98C>G (RAF1) ENSP00000401088.1:n.*1201+98C>G
ENST00000432427.3:c.853+98C>G (RAF1)
ENST00000460610.2:n.5379C>G (RAF1)
ENST00000471449.2:n.346+98C>G (RAF1)
ENST00000475353.2:n.3347C>G (RAF1)
ENST00000684903.1:c.*1213+98C>G (RAF1) ENSP00000508612.1:n.*1213+98C>G
ENST00000685348.1:c.*1095-177C>G (RAF1) ENSP00000510285.1:n.*1095-177C>G
ENST00000685437.1:c.1437+98C>G (RAF1) ENSP00000508794.1:n.1437+98C>G
ENST00000685653.1:c.1536+98C>G (RAF1) ENSP00000509968.1:n.1536+98C>G
ENST00000685697.1:n.2271+98C>G (RAF1)
ENST00000685738.1:c.*500+98C>G (RAF1) ENSP00000510156.1:n.*500+98C>G
ENST00000686409.1:n.4476C>G (RAF1)
ENST00000686455.1:n.3788C>G (RAF1)
ENST00000686762.1:c.*95+98C>G (RAF1) ENSP00000509767.1:n.*95+98C>G
ENST00000687257.1:n.3661C>G (RAF1)
ENST00000687326.1:c.*2359C>G (RAF1) ENSP00000509665.1:n.*2359C>G
ENST00000687505.1:n.1654+98C>G (RAF1)
ENST00000687923.1:c.1425+98C>G (RAF1) ENSP00000510255.1:n.1425+98C>G
ENST00000688269.1:n.2132+98C>G (RAF1)
ENST00000688444.1:n.3653+98C>G (RAF1)
ENST00000688543.1:c.1437+98C>G (RAF1) ENSP00000509612.1:n.1437+98C>G
ENST00000688625.1:c.*2905+98C>G (RAF1) ENSP00000509522.1:n.*2905+98C>G
ENST00000688803.1:n.2965-330C>G (RAF1)
ENST00000688914.1:n.620C>G (RAF1)
ENST00000689097.1:c.*1213+98C>G (RAF1) ENSP00000509756.1:n.*1213+98C>G
ENST00000689389.1:c.1359+98C>G (RAF1) ENSP00000510213.1:n.1359+98C>G
ENST00000689418.1:c.*3102C>G (RAF1) ENSP00000509467.1:n.*3102C>G
ENST00000689540.1:n.3575C>G (RAF1)
ENST00000689876.1:c.1418-177C>G (RAF1) ENSP00000508535.1:n.1418-177C>G
ENST00000689914.1:c.*470+98C>G (RAF1) ENSP00000509847.1:n.*470+98C>G
ENST00000690397.1:c.1425+98C>G (RAF1) ENSP00000508730.1:n.1425+98C>G
ENST00000690460.1:c.1524+98C>G (RAF1) ENSP00000509106.1:n.1524+98C>G
ENST00000690585.1:c.263-330C>G (RAF1)
ENST00000690625.1:n.2572+98C>G (RAF1)
ENST00000691396.1:c.*1408+98C>G (RAF1) ENSP00000510712.1:n.*1408+98C>G
ENST00000691643.1:n.2260C>G (RAF1)
ENST00000691724.1:c.*493+98C>G (RAF1) ENSP00000509255.1:n.*493+98C>G
ENST00000691779.1:c.*1114+98C>G (RAF1) ENSP00000508592.1:n.*1114+98C>G
ENST00000691888.1:c.410+98C>G (RAF1)
ENST00000691899.1:c.1536+98C>G (RAF1) ENSP00000508763.1:n.1536+98C>G
ENST00000692069.1:n.3991C>G (RAF1)
ENST00000692093.1:c.1437+98C>G (RAF1) ENSP00000509669.1:n.1437+98C>G
ENST00000692311.1:n.2360+98C>G (RAF1)
ENST00000692558.1:n.3790C>G (RAF1)
ENST00000692773.1:c.*1273+98C>G (RAF1) ENSP00000509055.1:n.*1273+98C>G
ENST00000692830.1:c.*1281+98C>G (RAF1) ENSP00000509461.1:n.*1281+98C>G
ENST00000693312.1:c.1311+98C>G (RAF1) ENSP00000508686.1:n.1311+98C>G
ENST00000693664.1:c.1488-330C>G (RAF1) ENSP00000509614.1:n.1488-330C>G
ENST00000693705.1:c.*1048-602C>G (RAF1) ENSP00000510697.1:n.*1048-602C>G
ENST00000251849.9:c.1536+98C>G (RAF1) MANE Select ENSP00000251849.4:n.1536+98C>G
ENST00000442415.7:c.1596+98C>G (RAF1) ENSP00000401888.2:n.1596+98C>G
ENST00000676541.1:c.*3330G>C (MKRN2) ENSP00000503730.1:n.*3330G>C
ENST00000677142.1:c.*3330G>C (MKRN2) ENSP00000504455.1:n.*3330G>C
ENST00000677816.1:c.*1885G>C (MKRN2) ENSP00000502893.1:n.*1885G>C
ENST00000677941.1:n.3393G>C (MKRN2)
ENST00000251849.8:c.1536+98C>G (RAF1) ENSP00000251849.4:n.1536+98C>G
ENST00000423275.5:c.*1213+98C>G (RAF1) ENSP00000401088.1:n.*1213+98C>G
ENST00000432427.2:c.1173+98C>G (RAF1) ENSP00000398591.2:n.1173+98C>G
ENST00000442415.6:c.1596+98C>G (RAF1) ENSP00000401888.2:n.1596+98C>G
ENST00000471449.1:n.225+98C>G (RAF1)
NM_002880.3:c.1536+98C>G , LRG_413t1:c.1536+98C>G (RAF1) NP_002871.1:n.1536+98C>G
XM_005265355.1:c.1536+98C>G (RAF1) XP_005265412.1:n.1536+98C>G
XM_005265357.1:c.1437+98C>G (RAF1) XP_005265414.1:n.1437+98C>G
XM_005265358.3:c.1293+98C>G (RAF1) XP_005265415.1:n.1293+98C>G
XM_005265359.3:c.1194+98C>G (RAF1) XP_005265416.1:n.1194+98C>G
XM_005265360.1:c.1418-177C>G (RAF1) XP_005265417.1:n.1418-177C>G
XM_011533974.1:c.1536+98C>G (RAF1) XP_011532276.1:n.1536+98C>G
XM_011533975.1:c.1293+98C>G (RAF1) XP_011532277.1:n.1293+98C>G
NM_001354689.1:c.1596+98C>G (RAF1) NP_001341618.1:n.1596+98C>G
NM_001354690.1:c.1536+98C>G (RAF1) NP_001341619.1:n.1536+98C>G
NM_001354691.1:c.1293+98C>G (RAF1) NP_001341620.1:n.1293+98C>G
NM_001354692.1:c.1293+98C>G (RAF1) NP_001341621.1:n.1293+98C>G
NM_001354693.1:c.1437+98C>G (RAF1) NP_001341622.1:n.1437+98C>G
NM_001354694.1:c.1353+98C>G (RAF1) NP_001341623.1:n.1353+98C>G
NM_001354695.1:c.1194+98C>G (RAF1) NP_001341624.1:n.1194+98C>G
NR_148940.1:n.2064+98C>G (RAF1)
NR_148941.1:n.2010+98C>G (RAF1)
NR_148942.1:n.1949+98C>G (RAF1)
XM_011533974.3:c.1536+98C>G (RAF1) XP_011532276.1:n.1536+98C>G
XM_017006966.1:c.1437+98C>G (RAF1) XP_016862455.1:n.1437+98C>G
NM_001354689.3:c.1596+98C>G (RAF1) NP_001341618.1:n.1596+98C>G
NM_001354690.2:c.1536+98C>G (RAF1) NP_001341619.1:n.1536+98C>G
NM_001354691.2:c.1293+98C>G (RAF1) NP_001341620.1:n.1293+98C>G
NM_001354692.2:c.1293+98C>G (RAF1) NP_001341621.1:n.1293+98C>G
NM_001354693.2:c.1437+98C>G (RAF1) NP_001341622.1:n.1437+98C>G
NM_001354694.2:c.1353+98C>G (RAF1) NP_001341623.1:n.1353+98C>G
NM_001354695.2:c.1194+98C>G (RAF1) NP_001341624.1:n.1194+98C>G
NR_148940.2:n.1980+98C>G (RAF1)
NR_148941.2:n.1926+98C>G (RAF1)
NR_148942.2:n.1865+98C>G (RAF1)
NM_001354690.3:c.1536+98C>G (RAF1) NP_001341619.1:n.1536+98C>G
NM_001354691.3:c.1293+98C>G (RAF1) NP_001341620.1:n.1293+98C>G
NM_001354692.3:c.1293+98C>G (RAF1) NP_001341621.1:n.1293+98C>G
NM_001354693.3:c.1437+98C>G (RAF1) NP_001341622.1:n.1437+98C>G
NM_001354694.3:c.1353+98C>G (RAF1) NP_001341623.1:n.1353+98C>G
NM_001354695.3:c.1194+98C>G (RAF1) NP_001341624.1:n.1194+98C>G
NM_002880.4:c.1536+98C>G (RAF1) MANE Select NP_002871.1:n.1536+98C>G
NR_148940.3:n.1980+98C>G (RAF1)
NR_148941.3:n.1926+98C>G (RAF1)
NR_148942.3:n.1865+98C>G (RAF1)