Canonical Allele Identifier: CA2664506523

Linked Data

gnomAD v4: 3-12584268-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584268C>T , CM000665.2:g.12584268C>T GRCh38
NC_000003.11:g.12625767C>T , CM000665.1:g.12625767C>T GRCh37
NC_000003.10:g.12600767C>T NCBI36
NG_007467.1:g.84912G>A , LRG_413:g.84912G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1858G>A (RAF1) ENSP00000401088.1:n.*1858G>A
ENST00000432427.3:c.1510G>A (RAF1)
ENST00000460610.2:n.6505G>A (RAF1)
ENST00000471449.2:n.1003G>A (RAF1)
ENST00000475353.2:n.4473G>A (RAF1)
ENST00000684903.1:c.*1870G>A (RAF1) ENSP00000508612.1:n.*1870G>A
ENST00000685348.1:c.*1904G>A (RAF1) ENSP00000510285.1:n.*1904G>A
ENST00000685437.1:c.*246G>A (RAF1) ENSP00000508794.1:n.*246G>A
ENST00000685653.1:c.*246G>A (RAF1) ENSP00000509968.1:n.*246G>A
ENST00000685697.1:n.2928G>A (RAF1)
ENST00000685738.1:c.*1157G>A (RAF1) ENSP00000510156.1:n.*1157G>A
ENST00000686409.1:n.5602G>A (RAF1)
ENST00000686455.1:n.4914G>A (RAF1)
ENST00000686762.1:c.*752G>A (RAF1) ENSP00000509767.1:n.*752G>A
ENST00000687257.1:n.4647G>A (RAF1)
ENST00000687326.1:c.*3485G>A (RAF1) ENSP00000509665.1:n.*3485G>A
ENST00000687505.1:n.2311G>A (RAF1)
ENST00000687923.1:c.*246G>A (RAF1) ENSP00000510255.1:n.*246G>A
ENST00000688269.1:n.2789G>A (RAF1)
ENST00000688444.1:n.4310G>A (RAF1)
ENST00000688543.1:c.*246G>A (RAF1) ENSP00000509612.1:n.*246G>A
ENST00000688625.1:c.*3562G>A (RAF1) ENSP00000509522.1:n.*3562G>A
ENST00000688803.1:n.3621G>A (RAF1)
ENST00000689097.1:c.*1870G>A (RAF1) ENSP00000509756.1:n.*1870G>A
ENST00000689389.1:c.*246G>A (RAF1) ENSP00000510213.1:n.*246G>A
ENST00000689418.1:c.*4088G>A (RAF1) ENSP00000509467.1:n.*4088G>A
ENST00000689540.1:n.4561G>A (RAF1)
ENST00000689876.1:c.*742G>A (RAF1) ENSP00000508535.1:n.*742G>A
ENST00000689914.1:c.*1127G>A (RAF1) ENSP00000509847.1:n.*1127G>A
ENST00000690397.1:c.*246G>A (RAF1) ENSP00000508730.1:n.*246G>A
ENST00000690460.1:c.*246G>A (RAF1) ENSP00000509106.1:n.*246G>A
ENST00000690585.1:c.919G>A (RAF1)
ENST00000690625.1:n.3229G>A (RAF1)
ENST00000691396.1:c.*2065G>A (RAF1) ENSP00000510712.1:n.*2065G>A
ENST00000691643.1:n.3246G>A (RAF1)
ENST00000691724.1:c.*1150G>A (RAF1) ENSP00000509255.1:n.*1150G>A
ENST00000691779.1:c.*1771G>A (RAF1) ENSP00000508592.1:n.*1771G>A
ENST00000691888.1:c.1067G>A (RAF1)
ENST00000691899.1:c.*246G>A (RAF1) ENSP00000508763.1:n.*246G>A
ENST00000692069.1:n.5117G>A (RAF1)
ENST00000692093.1:c.*246G>A (RAF1) ENSP00000509669.1:n.*246G>A
ENST00000692311.1:n.3017G>A (RAF1)
ENST00000692558.1:n.4776G>A (RAF1)
ENST00000692773.1:c.*1930G>A (RAF1) ENSP00000509055.1:n.*1930G>A
ENST00000692830.1:c.*1938G>A (RAF1) ENSP00000509461.1:n.*1938G>A
ENST00000693312.1:c.*246G>A (RAF1) ENSP00000508686.1:n.*246G>A
ENST00000693664.1:c.*644G>A (RAF1) ENSP00000509614.1:n.*644G>A
ENST00000693705.1:c.*1572G>A (RAF1) ENSP00000510697.1:n.*1572G>A
ENST00000251849.9:c.*246G>A (RAF1) MANE Select ENSP00000251849.4:n.*246G>A
ENST00000442415.7:c.*246G>A (RAF1) ENSP00000401888.2:n.*246G>A
ENST00000676541.1:c.*2015C>T (MKRN2) ENSP00000503730.1:n.*2015C>T
ENST00000677142.1:c.*2015C>T (MKRN2) ENSP00000504455.1:n.*2015C>T
ENST00000677816.1:c.*570C>T (MKRN2) ENSP00000502893.1:n.*570C>T
ENST00000677941.1:n.2078C>T (MKRN2)
ENST00000251849.8:c.*246G>A (RAF1) ENSP00000251849.4:n.*246G>A
ENST00000432427.2:c.1830G>A (RAF1) ENSP00000398591.2:n.1830G>A
ENST00000442415.6:c.*246G>A (RAF1) ENSP00000401888.2:n.*246G>A
NM_002880.3:c.*246G>A , LRG_413t1:c.*246G>A (RAF1) NP_002871.1:n.*246G>A
XM_005265355.1:c.*246G>A (RAF1) XP_005265412.1:n.*246G>A
XM_005265357.1:c.*246G>A (RAF1) XP_005265414.1:n.*246G>A
XM_005265358.3:c.*246G>A (RAF1) XP_005265415.1:n.*246G>A
XM_005265359.3:c.*246G>A (RAF1) XP_005265416.1:n.*246G>A
XM_011533974.1:c.*246G>A (RAF1) XP_011532276.1:n.*246G>A
XM_011533975.1:c.*246G>A (RAF1) XP_011532277.1:n.*246G>A
NM_001354689.1:c.*246G>A (RAF1) NP_001341618.1:n.*246G>A
NM_001354690.1:c.*246G>A (RAF1) NP_001341619.1:n.*246G>A
NM_001354691.1:c.*246G>A (RAF1) NP_001341620.1:n.*246G>A
NM_001354692.1:c.*246G>A (RAF1) NP_001341621.1:n.*246G>A
NM_001354693.1:c.*246G>A (RAF1) NP_001341622.1:n.*246G>A
NM_001354694.1:c.*246G>A (RAF1) NP_001341623.1:n.*246G>A
NM_001354695.1:c.*246G>A (RAF1) NP_001341624.1:n.*246G>A
NR_148940.1:n.2721G>A (RAF1)
NR_148941.1:n.2667G>A (RAF1)
NR_148942.1:n.2606G>A (RAF1)
XM_011533974.3:c.*246G>A (RAF1) XP_011532276.1:n.*246G>A
XM_017006966.1:c.*246G>A (RAF1) XP_016862455.1:n.*246G>A
NM_001354689.3:c.*246G>A (RAF1) NP_001341618.1:n.*246G>A
NM_001354690.2:c.*246G>A (RAF1) NP_001341619.1:n.*246G>A
NM_001354691.2:c.*246G>A (RAF1) NP_001341620.1:n.*246G>A
NM_001354692.2:c.*246G>A (RAF1) NP_001341621.1:n.*246G>A
NM_001354693.2:c.*246G>A (RAF1) NP_001341622.1:n.*246G>A
NM_001354694.2:c.*246G>A (RAF1) NP_001341623.1:n.*246G>A
NM_001354695.2:c.*246G>A (RAF1) NP_001341624.1:n.*246G>A
NR_148940.2:n.2637G>A (RAF1)
NR_148941.2:n.2583G>A (RAF1)
NR_148942.2:n.2522G>A (RAF1)
NM_001354690.3:c.*246G>A (RAF1) NP_001341619.1:n.*246G>A
NM_001354691.3:c.*246G>A (RAF1) NP_001341620.1:n.*246G>A
NM_001354692.3:c.*246G>A (RAF1) NP_001341621.1:n.*246G>A
NM_001354693.3:c.*246G>A (RAF1) NP_001341622.1:n.*246G>A
NM_001354694.3:c.*246G>A (RAF1) NP_001341623.1:n.*246G>A
NM_001354695.3:c.*246G>A (RAF1) NP_001341624.1:n.*246G>A
NM_002880.4:c.*246G>A (RAF1) MANE Select NP_002871.1:n.*246G>A
NR_148940.3:n.2637G>A (RAF1)
NR_148941.3:n.2583G>A (RAF1)
NR_148942.3:n.2522G>A (RAF1)