Canonical Allele Identifier: CA69601796
Gene: RAF1 HGNC NCBI
MKRN2 HGNC NCBI

Linked Data

dbSNP Id: rs926614729
gnomAD v4: 3-12584343-G-T
MyVariant Identifiers: chr3:g.12625842G>T (hg19) chr3:g.12584343G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584343G>T , CM000665.2:g.12584343G>T GRCh38
NC_000003.11:g.12625842G>T , CM000665.1:g.12625842G>T GRCh37
NC_000003.10:g.12600842G>T NCBI36
NG_007467.1:g.84837C>A , LRG_413:g.84837C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1783C>A (RAF1) ENSP00000401088.1:n.*1783C>A
ENST00000432427.3:c.1435C>A (RAF1)
ENST00000460610.2:n.6430C>A (RAF1)
ENST00000471449.2:n.928C>A (RAF1)
ENST00000475353.2:n.4398C>A (RAF1)
ENST00000684903.1:c.*1795C>A (RAF1) ENSP00000508612.1:n.*1795C>A
ENST00000685348.1:c.*1829C>A (RAF1) ENSP00000510285.1:n.*1829C>A
ENST00000685437.1:c.*171C>A (RAF1) ENSP00000508794.1:n.*171C>A
ENST00000685653.1:c.*171C>A (RAF1) ENSP00000509968.1:n.*171C>A
ENST00000685697.1:n.2853C>A (RAF1)
ENST00000685738.1:c.*1082C>A (RAF1) ENSP00000510156.1:n.*1082C>A
ENST00000686409.1:n.5527C>A (RAF1)
ENST00000686455.1:n.4839C>A (RAF1)
ENST00000686762.1:c.*677C>A (RAF1) ENSP00000509767.1:n.*677C>A
ENST00000687257.1:n.4572C>A (RAF1)
ENST00000687326.1:c.*3410C>A (RAF1) ENSP00000509665.1:n.*3410C>A
ENST00000687505.1:n.2236C>A (RAF1)
ENST00000687923.1:c.*171C>A (RAF1) ENSP00000510255.1:n.*171C>A
ENST00000688269.1:n.2714C>A (RAF1)
ENST00000688444.1:n.4235C>A (RAF1)
ENST00000688543.1:c.*171C>A (RAF1) ENSP00000509612.1:n.*171C>A
ENST00000688625.1:c.*3487C>A (RAF1) ENSP00000509522.1:n.*3487C>A
ENST00000688803.1:n.3546C>A (RAF1)
ENST00000689097.1:c.*1795C>A (RAF1) ENSP00000509756.1:n.*1795C>A
ENST00000689389.1:c.*171C>A (RAF1) ENSP00000510213.1:n.*171C>A
ENST00000689418.1:c.*4013C>A (RAF1) ENSP00000509467.1:n.*4013C>A
ENST00000689540.1:n.4486C>A (RAF1)
ENST00000689876.1:c.*667C>A (RAF1) ENSP00000508535.1:n.*667C>A
ENST00000689914.1:c.*1052C>A (RAF1) ENSP00000509847.1:n.*1052C>A
ENST00000690397.1:c.*171C>A (RAF1) ENSP00000508730.1:n.*171C>A
ENST00000690460.1:c.*171C>A (RAF1) ENSP00000509106.1:n.*171C>A
ENST00000690585.1:c.844C>A (RAF1)
ENST00000690625.1:n.3154C>A (RAF1)
ENST00000691396.1:c.*1990C>A (RAF1) ENSP00000510712.1:n.*1990C>A
ENST00000691643.1:n.3171C>A (RAF1)
ENST00000691724.1:c.*1075C>A (RAF1) ENSP00000509255.1:n.*1075C>A
ENST00000691779.1:c.*1696C>A (RAF1) ENSP00000508592.1:n.*1696C>A
ENST00000691888.1:c.992C>A (RAF1)
ENST00000691899.1:c.*171C>A (RAF1) ENSP00000508763.1:n.*171C>A
ENST00000692069.1:n.5042C>A (RAF1)
ENST00000692093.1:c.*171C>A (RAF1) ENSP00000509669.1:n.*171C>A
ENST00000692311.1:n.2942C>A (RAF1)
ENST00000692558.1:n.4701C>A (RAF1)
ENST00000692773.1:c.*1855C>A (RAF1) ENSP00000509055.1:n.*1855C>A
ENST00000692830.1:c.*1863C>A (RAF1) ENSP00000509461.1:n.*1863C>A
ENST00000693312.1:c.*171C>A (RAF1) ENSP00000508686.1:n.*171C>A
ENST00000693664.1:c.*569C>A (RAF1) ENSP00000509614.1:n.*569C>A
ENST00000693705.1:c.*1497C>A (RAF1) ENSP00000510697.1:n.*1497C>A
ENST00000251849.9:c.*171C>A (RAF1) MANE Select ENSP00000251849.4:n.*171C>A
ENST00000442415.7:c.*171C>A (RAF1) ENSP00000401888.2:n.*171C>A
ENST00000676541.1:c.*2090G>T (MKRN2) ENSP00000503730.1:n.*2090G>T
ENST00000677142.1:c.*2090G>T (MKRN2) ENSP00000504455.1:n.*2090G>T
ENST00000677816.1:c.*645G>T (MKRN2) ENSP00000502893.1:n.*645G>T
ENST00000677941.1:n.2153G>T (MKRN2)
ENST00000251849.8:c.*171C>A (RAF1) ENSP00000251849.4:n.*171C>A
ENST00000423275.5:c.*1795C>A (RAF1) ENSP00000401088.1:n.*1795C>A
ENST00000432427.2:c.1755C>A (RAF1) ENSP00000398591.2:n.1755C>A
ENST00000442415.6:c.*171C>A (RAF1) ENSP00000401888.2:n.*171C>A
NM_002880.3:c.*171C>A , LRG_413t1:c.*171C>A (RAF1) NP_002871.1:n.*171C>A
XM_005265355.1:c.*171C>A (RAF1) XP_005265412.1:n.*171C>A
XM_005265357.1:c.*171C>A (RAF1) XP_005265414.1:n.*171C>A
XM_005265358.3:c.*171C>A (RAF1) XP_005265415.1:n.*171C>A
XM_005265359.3:c.*171C>A (RAF1) XP_005265416.1:n.*171C>A
XM_011533974.1:c.*171C>A (RAF1) XP_011532276.1:n.*171C>A
XM_011533975.1:c.*171C>A (RAF1) XP_011532277.1:n.*171C>A
NM_001354689.1:c.*171C>A (RAF1) NP_001341618.1:n.*171C>A
NM_001354690.1:c.*171C>A (RAF1) NP_001341619.1:n.*171C>A
NM_001354691.1:c.*171C>A (RAF1) NP_001341620.1:n.*171C>A
NM_001354692.1:c.*171C>A (RAF1) NP_001341621.1:n.*171C>A
NM_001354693.1:c.*171C>A (RAF1) NP_001341622.1:n.*171C>A
NM_001354694.1:c.*171C>A (RAF1) NP_001341623.1:n.*171C>A
NM_001354695.1:c.*171C>A (RAF1) NP_001341624.1:n.*171C>A
NR_148940.1:n.2646C>A (RAF1)
NR_148941.1:n.2592C>A (RAF1)
NR_148942.1:n.2531C>A (RAF1)
XM_011533974.3:c.*171C>A (RAF1) XP_011532276.1:n.*171C>A
XM_017006966.1:c.*171C>A (RAF1) XP_016862455.1:n.*171C>A
NM_001354689.3:c.*171C>A (RAF1) NP_001341618.1:n.*171C>A
NM_001354690.2:c.*171C>A (RAF1) NP_001341619.1:n.*171C>A
NM_001354691.2:c.*171C>A (RAF1) NP_001341620.1:n.*171C>A
NM_001354692.2:c.*171C>A (RAF1) NP_001341621.1:n.*171C>A
NM_001354693.2:c.*171C>A (RAF1) NP_001341622.1:n.*171C>A
NM_001354694.2:c.*171C>A (RAF1) NP_001341623.1:n.*171C>A
NM_001354695.2:c.*171C>A (RAF1) NP_001341624.1:n.*171C>A
NR_148940.2:n.2562C>A (RAF1)
NR_148941.2:n.2508C>A (RAF1)
NR_148942.2:n.2447C>A (RAF1)
NM_001354690.3:c.*171C>A (RAF1) NP_001341619.1:n.*171C>A
NM_001354691.3:c.*171C>A (RAF1) NP_001341620.1:n.*171C>A
NM_001354692.3:c.*171C>A (RAF1) NP_001341621.1:n.*171C>A
NM_001354693.3:c.*171C>A (RAF1) NP_001341622.1:n.*171C>A
NM_001354694.3:c.*171C>A (RAF1) NP_001341623.1:n.*171C>A
NM_001354695.3:c.*171C>A (RAF1) NP_001341624.1:n.*171C>A
NM_002880.4:c.*171C>A (RAF1) MANE Select NP_002871.1:n.*171C>A
NR_148940.3:n.2562C>A (RAF1)
NR_148941.3:n.2508C>A (RAF1)
NR_148942.3:n.2447C>A (RAF1)
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