Canonical Allele Identifier: CA2664506648

Linked Data

gnomAD v4: 3-12584345-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584345G>T , CM000665.2:g.12584345G>T GRCh38
NC_000003.11:g.12625844G>T , CM000665.1:g.12625844G>T GRCh37
NC_000003.10:g.12600844G>T NCBI36
NG_007467.1:g.84835C>A , LRG_413:g.84835C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1781C>A (RAF1) ENSP00000401088.1:n.*1781C>A
ENST00000432427.3:c.1433C>A (RAF1)
ENST00000460610.2:n.6428C>A (RAF1)
ENST00000471449.2:n.926C>A (RAF1)
ENST00000475353.2:n.4396C>A (RAF1)
ENST00000684903.1:c.*1793C>A (RAF1) ENSP00000508612.1:n.*1793C>A
ENST00000685348.1:c.*1827C>A (RAF1) ENSP00000510285.1:n.*1827C>A
ENST00000685437.1:c.*169C>A (RAF1) ENSP00000508794.1:n.*169C>A
ENST00000685653.1:c.*169C>A (RAF1) ENSP00000509968.1:n.*169C>A
ENST00000685697.1:n.2851C>A (RAF1)
ENST00000685738.1:c.*1080C>A (RAF1) ENSP00000510156.1:n.*1080C>A
ENST00000686409.1:n.5525C>A (RAF1)
ENST00000686455.1:n.4837C>A (RAF1)
ENST00000686762.1:c.*675C>A (RAF1) ENSP00000509767.1:n.*675C>A
ENST00000687257.1:n.4570C>A (RAF1)
ENST00000687326.1:c.*3408C>A (RAF1) ENSP00000509665.1:n.*3408C>A
ENST00000687505.1:n.2234C>A (RAF1)
ENST00000687923.1:c.*169C>A (RAF1) ENSP00000510255.1:n.*169C>A
ENST00000688269.1:n.2712C>A (RAF1)
ENST00000688444.1:n.4233C>A (RAF1)
ENST00000688543.1:c.*169C>A (RAF1) ENSP00000509612.1:n.*169C>A
ENST00000688625.1:c.*3485C>A (RAF1) ENSP00000509522.1:n.*3485C>A
ENST00000688803.1:n.3544C>A (RAF1)
ENST00000689097.1:c.*1793C>A (RAF1) ENSP00000509756.1:n.*1793C>A
ENST00000689389.1:c.*169C>A (RAF1) ENSP00000510213.1:n.*169C>A
ENST00000689418.1:c.*4011C>A (RAF1) ENSP00000509467.1:n.*4011C>A
ENST00000689540.1:n.4484C>A (RAF1)
ENST00000689876.1:c.*665C>A (RAF1) ENSP00000508535.1:n.*665C>A
ENST00000689914.1:c.*1050C>A (RAF1) ENSP00000509847.1:n.*1050C>A
ENST00000690397.1:c.*169C>A (RAF1) ENSP00000508730.1:n.*169C>A
ENST00000690460.1:c.*169C>A (RAF1) ENSP00000509106.1:n.*169C>A
ENST00000690585.1:c.842C>A (RAF1)
ENST00000690625.1:n.3152C>A (RAF1)
ENST00000691396.1:c.*1988C>A (RAF1) ENSP00000510712.1:n.*1988C>A
ENST00000691643.1:n.3169C>A (RAF1)
ENST00000691724.1:c.*1073C>A (RAF1) ENSP00000509255.1:n.*1073C>A
ENST00000691779.1:c.*1694C>A (RAF1) ENSP00000508592.1:n.*1694C>A
ENST00000691888.1:c.990C>A (RAF1)
ENST00000691899.1:c.*169C>A (RAF1) ENSP00000508763.1:n.*169C>A
ENST00000692069.1:n.5040C>A (RAF1)
ENST00000692093.1:c.*169C>A (RAF1) ENSP00000509669.1:n.*169C>A
ENST00000692311.1:n.2940C>A (RAF1)
ENST00000692558.1:n.4699C>A (RAF1)
ENST00000692773.1:c.*1853C>A (RAF1) ENSP00000509055.1:n.*1853C>A
ENST00000692830.1:c.*1861C>A (RAF1) ENSP00000509461.1:n.*1861C>A
ENST00000693312.1:c.*169C>A (RAF1) ENSP00000508686.1:n.*169C>A
ENST00000693664.1:c.*567C>A (RAF1) ENSP00000509614.1:n.*567C>A
ENST00000693705.1:c.*1495C>A (RAF1) ENSP00000510697.1:n.*1495C>A
ENST00000251849.9:c.*169C>A (RAF1) MANE Select ENSP00000251849.4:n.*169C>A
ENST00000442415.7:c.*169C>A (RAF1) ENSP00000401888.2:n.*169C>A
ENST00000676541.1:c.*2092G>T (MKRN2) ENSP00000503730.1:n.*2092G>T
ENST00000677142.1:c.*2092G>T (MKRN2) ENSP00000504455.1:n.*2092G>T
ENST00000677816.1:c.*647G>T (MKRN2) ENSP00000502893.1:n.*647G>T
ENST00000677941.1:n.2155G>T (MKRN2)
ENST00000251849.8:c.*169C>A (RAF1) ENSP00000251849.4:n.*169C>A
ENST00000423275.5:c.*1793C>A (RAF1) ENSP00000401088.1:n.*1793C>A
ENST00000432427.2:c.1753C>A (RAF1) ENSP00000398591.2:n.1753C>A
ENST00000442415.6:c.*169C>A (RAF1) ENSP00000401888.2:n.*169C>A
NM_002880.3:c.*169C>A , LRG_413t1:c.*169C>A (RAF1) NP_002871.1:n.*169C>A
XM_005265355.1:c.*169C>A (RAF1) XP_005265412.1:n.*169C>A
XM_005265357.1:c.*169C>A (RAF1) XP_005265414.1:n.*169C>A
XM_005265358.3:c.*169C>A (RAF1) XP_005265415.1:n.*169C>A
XM_005265359.3:c.*169C>A (RAF1) XP_005265416.1:n.*169C>A
XM_011533974.1:c.*169C>A (RAF1) XP_011532276.1:n.*169C>A
XM_011533975.1:c.*169C>A (RAF1) XP_011532277.1:n.*169C>A
NM_001354689.1:c.*169C>A (RAF1) NP_001341618.1:n.*169C>A
NM_001354690.1:c.*169C>A (RAF1) NP_001341619.1:n.*169C>A
NM_001354691.1:c.*169C>A (RAF1) NP_001341620.1:n.*169C>A
NM_001354692.1:c.*169C>A (RAF1) NP_001341621.1:n.*169C>A
NM_001354693.1:c.*169C>A (RAF1) NP_001341622.1:n.*169C>A
NM_001354694.1:c.*169C>A (RAF1) NP_001341623.1:n.*169C>A
NM_001354695.1:c.*169C>A (RAF1) NP_001341624.1:n.*169C>A
NR_148940.1:n.2644C>A (RAF1)
NR_148941.1:n.2590C>A (RAF1)
NR_148942.1:n.2529C>A (RAF1)
XM_011533974.3:c.*169C>A (RAF1) XP_011532276.1:n.*169C>A
XM_017006966.1:c.*169C>A (RAF1) XP_016862455.1:n.*169C>A
NM_001354689.3:c.*169C>A (RAF1) NP_001341618.1:n.*169C>A
NM_001354690.2:c.*169C>A (RAF1) NP_001341619.1:n.*169C>A
NM_001354691.2:c.*169C>A (RAF1) NP_001341620.1:n.*169C>A
NM_001354692.2:c.*169C>A (RAF1) NP_001341621.1:n.*169C>A
NM_001354693.2:c.*169C>A (RAF1) NP_001341622.1:n.*169C>A
NM_001354694.2:c.*169C>A (RAF1) NP_001341623.1:n.*169C>A
NM_001354695.2:c.*169C>A (RAF1) NP_001341624.1:n.*169C>A
NR_148940.2:n.2560C>A (RAF1)
NR_148941.2:n.2506C>A (RAF1)
NR_148942.2:n.2445C>A (RAF1)
NM_001354690.3:c.*169C>A (RAF1) NP_001341619.1:n.*169C>A
NM_001354691.3:c.*169C>A (RAF1) NP_001341620.1:n.*169C>A
NM_001354692.3:c.*169C>A (RAF1) NP_001341621.1:n.*169C>A
NM_001354693.3:c.*169C>A (RAF1) NP_001341622.1:n.*169C>A
NM_001354694.3:c.*169C>A (RAF1) NP_001341623.1:n.*169C>A
NM_001354695.3:c.*169C>A (RAF1) NP_001341624.1:n.*169C>A
NM_002880.4:c.*169C>A (RAF1) MANE Select NP_002871.1:n.*169C>A
NR_148940.3:n.2560C>A (RAF1)
NR_148941.3:n.2506C>A (RAF1)
NR_148942.3:n.2445C>A (RAF1)