Canonical Allele Identifier: CA2664506800

Linked Data

dbSNP Id: rs2125315048
gnomAD v4: 3-12584451-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584451G>A , CM000665.2:g.12584451G>A GRCh38
NC_000003.11:g.12625950G>A , CM000665.1:g.12625950G>A GRCh37
NC_000003.10:g.12600950G>A NCBI36
NG_007467.1:g.84729C>T , LRG_413:g.84729C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1675C>T (RAF1) ENSP00000401088.1:n.*1675C>T
ENST00000432427.3:c.1327C>T (RAF1)
ENST00000460610.2:n.6322C>T (RAF1)
ENST00000471449.2:n.820C>T (RAF1)
ENST00000475353.2:n.4290C>T (RAF1)
ENST00000684903.1:c.*1687C>T (RAF1) ENSP00000508612.1:n.*1687C>T
ENST00000685348.1:c.*1721C>T (RAF1) ENSP00000510285.1:n.*1721C>T
ENST00000685437.1:c.*63C>T (RAF1) ENSP00000508794.1:n.*63C>T
ENST00000685653.1:c.*63C>T (RAF1) ENSP00000509968.1:n.*63C>T
ENST00000685697.1:n.2745C>T (RAF1)
ENST00000685738.1:c.*974C>T (RAF1) ENSP00000510156.1:n.*974C>T
ENST00000686409.1:n.5419C>T (RAF1)
ENST00000686455.1:n.4731C>T (RAF1)
ENST00000686762.1:c.*569C>T (RAF1) ENSP00000509767.1:n.*569C>T
ENST00000687257.1:n.4464C>T (RAF1)
ENST00000687326.1:c.*3302C>T (RAF1) ENSP00000509665.1:n.*3302C>T
ENST00000687505.1:n.2128C>T (RAF1)
ENST00000687923.1:c.*63C>T (RAF1) ENSP00000510255.1:n.*63C>T
ENST00000688269.1:n.2606C>T (RAF1)
ENST00000688444.1:n.4127C>T (RAF1)
ENST00000688543.1:c.*63C>T (RAF1) ENSP00000509612.1:n.*63C>T
ENST00000688625.1:c.*3379C>T (RAF1) ENSP00000509522.1:n.*3379C>T
ENST00000688803.1:n.3438C>T (RAF1)
ENST00000689097.1:c.*1687C>T (RAF1) ENSP00000509756.1:n.*1687C>T
ENST00000689389.1:c.*63C>T (RAF1) ENSP00000510213.1:n.*63C>T
ENST00000689418.1:c.*3905C>T (RAF1) ENSP00000509467.1:n.*3905C>T
ENST00000689540.1:n.4378C>T (RAF1)
ENST00000689876.1:c.*559C>T (RAF1) ENSP00000508535.1:n.*559C>T
ENST00000689914.1:c.*944C>T (RAF1) ENSP00000509847.1:n.*944C>T
ENST00000690397.1:c.*63C>T (RAF1) ENSP00000508730.1:n.*63C>T
ENST00000690460.1:c.*63C>T (RAF1) ENSP00000509106.1:n.*63C>T
ENST00000690585.1:c.736C>T (RAF1)
ENST00000690625.1:n.3046C>T (RAF1)
ENST00000691396.1:c.*1882C>T (RAF1) ENSP00000510712.1:n.*1882C>T
ENST00000691643.1:n.3063C>T (RAF1)
ENST00000691724.1:c.*967C>T (RAF1) ENSP00000509255.1:n.*967C>T
ENST00000691779.1:c.*1588C>T (RAF1) ENSP00000508592.1:n.*1588C>T
ENST00000691888.1:c.884C>T (RAF1)
ENST00000691899.1:c.*63C>T (RAF1) ENSP00000508763.1:n.*63C>T
ENST00000692069.1:n.4934C>T (RAF1)
ENST00000692093.1:c.*63C>T (RAF1) ENSP00000509669.1:n.*63C>T
ENST00000692311.1:n.2834C>T (RAF1)
ENST00000692558.1:n.4593C>T (RAF1)
ENST00000692773.1:c.*1747C>T (RAF1) ENSP00000509055.1:n.*1747C>T
ENST00000692830.1:c.*1755C>T (RAF1) ENSP00000509461.1:n.*1755C>T
ENST00000693312.1:c.*63C>T (RAF1) ENSP00000508686.1:n.*63C>T
ENST00000693664.1:c.*461C>T (RAF1) ENSP00000509614.1:n.*461C>T
ENST00000693705.1:c.*1389C>T (RAF1) ENSP00000510697.1:n.*1389C>T
ENST00000251849.9:c.*63C>T (RAF1) MANE Select ENSP00000251849.4:n.*63C>T
ENST00000442415.7:c.*63C>T (RAF1) ENSP00000401888.2:n.*63C>T
ENST00000676541.1:c.*2198G>A (MKRN2) ENSP00000503730.1:n.*2198G>A
ENST00000677142.1:c.*2198G>A (MKRN2) ENSP00000504455.1:n.*2198G>A
ENST00000677816.1:c.*753G>A (MKRN2) ENSP00000502893.1:n.*753G>A
ENST00000677941.1:n.2261G>A (MKRN2)
ENST00000251849.8:c.*63C>T (RAF1) ENSP00000251849.4:n.*63C>T
ENST00000423275.5:c.*1687C>T (RAF1) ENSP00000401088.1:n.*1687C>T
ENST00000432427.2:c.1647C>T (RAF1) ENSP00000398591.2:n.1647C>T
ENST00000442415.6:c.*63C>T (RAF1) ENSP00000401888.2:n.*63C>T
ENST00000471449.1:n.699C>T (RAF1)
NM_002880.3:c.*63C>T , LRG_413t1:c.*63C>T (RAF1) NP_002871.1:n.*63C>T
XM_005265355.1:c.*63C>T (RAF1) XP_005265412.1:n.*63C>T
XM_005265357.1:c.*63C>T (RAF1) XP_005265414.1:n.*63C>T
XM_005265358.3:c.*63C>T (RAF1) XP_005265415.1:n.*63C>T
XM_005265359.3:c.*63C>T (RAF1) XP_005265416.1:n.*63C>T
XM_011533974.1:c.*63C>T (RAF1) XP_011532276.1:n.*63C>T
XM_011533975.1:c.*63C>T (RAF1) XP_011532277.1:n.*63C>T
NM_001354689.1:c.*63C>T (RAF1) NP_001341618.1:n.*63C>T
NM_001354690.1:c.*63C>T (RAF1) NP_001341619.1:n.*63C>T
NM_001354691.1:c.*63C>T (RAF1) NP_001341620.1:n.*63C>T
NM_001354692.1:c.*63C>T (RAF1) NP_001341621.1:n.*63C>T
NM_001354693.1:c.*63C>T (RAF1) NP_001341622.1:n.*63C>T
NM_001354694.1:c.*63C>T (RAF1) NP_001341623.1:n.*63C>T
NM_001354695.1:c.*63C>T (RAF1) NP_001341624.1:n.*63C>T
NR_148940.1:n.2538C>T (RAF1)
NR_148941.1:n.2484C>T (RAF1)
NR_148942.1:n.2423C>T (RAF1)
XM_011533974.3:c.*63C>T (RAF1) XP_011532276.1:n.*63C>T
XM_017006966.1:c.*63C>T (RAF1) XP_016862455.1:n.*63C>T
NM_001354689.3:c.*63C>T (RAF1) NP_001341618.1:n.*63C>T
NM_001354690.2:c.*63C>T (RAF1) NP_001341619.1:n.*63C>T
NM_001354691.2:c.*63C>T (RAF1) NP_001341620.1:n.*63C>T
NM_001354692.2:c.*63C>T (RAF1) NP_001341621.1:n.*63C>T
NM_001354693.2:c.*63C>T (RAF1) NP_001341622.1:n.*63C>T
NM_001354694.2:c.*63C>T (RAF1) NP_001341623.1:n.*63C>T
NM_001354695.2:c.*63C>T (RAF1) NP_001341624.1:n.*63C>T
NR_148940.2:n.2454C>T (RAF1)
NR_148941.2:n.2400C>T (RAF1)
NR_148942.2:n.2339C>T (RAF1)
NM_001354690.3:c.*63C>T (RAF1) NP_001341619.1:n.*63C>T
NM_001354691.3:c.*63C>T (RAF1) NP_001341620.1:n.*63C>T
NM_001354692.3:c.*63C>T (RAF1) NP_001341621.1:n.*63C>T
NM_001354693.3:c.*63C>T (RAF1) NP_001341622.1:n.*63C>T
NM_001354694.3:c.*63C>T (RAF1) NP_001341623.1:n.*63C>T
NM_001354695.3:c.*63C>T (RAF1) NP_001341624.1:n.*63C>T
NM_002880.4:c.*63C>T (RAF1) MANE Select NP_002871.1:n.*63C>T
NR_148940.3:n.2454C>T (RAF1)
NR_148941.3:n.2400C>T (RAF1)
NR_148942.3:n.2339C>T (RAF1)