Canonical Allele Identifier: CA432522009

Linked Data

MyVariant Identifiers: chr3:g.12626382C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584883C>G , CM000665.2:g.12584883C>G GRCh38
NC_000003.11:g.12626382C>G , CM000665.1:g.12626382C>G GRCh37
NC_000003.10:g.12601382C>G NCBI36
NG_007467.1:g.84297G>C , LRG_413:g.84297G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1432G>C (RAF1) ENSP00000401088.1:n.*1432G>C
ENST00000432427.3:c.1084G>C (RAF1)
ENST00000460610.2:n.6079G>C (RAF1)
ENST00000471449.2:n.577G>C (RAF1)
ENST00000475353.2:n.4047G>C (RAF1)
ENST00000684903.1:c.*1444G>C (RAF1) ENSP00000508612.1:n.*1444G>C
ENST00000685348.1:c.*1478G>C (RAF1) ENSP00000510285.1:n.*1478G>C
ENST00000685437.1:c.1668G>C (RAF1) ENSP00000508794.1:p.Val556=
ENST00000685653.1:c.1767G>C (RAF1) ENSP00000509968.1:p.Val589=
ENST00000685697.1:n.2502G>C (RAF1)
ENST00000685738.1:c.*731G>C (RAF1) ENSP00000510156.1:n.*731G>C
ENST00000686409.1:n.5176G>C (RAF1)
ENST00000686455.1:n.4488G>C (RAF1)
ENST00000686762.1:c.*326G>C (RAF1) ENSP00000509767.1:n.*326G>C
ENST00000687257.1:n.4221G>C (RAF1)
ENST00000687326.1:c.*3059G>C (RAF1) ENSP00000509665.1:n.*3059G>C
ENST00000687505.1:n.1885G>C (RAF1)
ENST00000687923.1:c.1656G>C (RAF1) ENSP00000510255.1:p.Val552=
ENST00000688269.1:n.2363G>C (RAF1)
ENST00000688444.1:n.3884G>C (RAF1)
ENST00000688543.1:c.1668G>C (RAF1) ENSP00000509612.1:p.Val556=
ENST00000688625.1:c.*3136G>C (RAF1) ENSP00000509522.1:n.*3136G>C
ENST00000688803.1:n.3195G>C (RAF1)
ENST00000689097.1:c.*1444G>C (RAF1) ENSP00000509756.1:n.*1444G>C
ENST00000689389.1:c.1590G>C (RAF1) ENSP00000510213.1:p.Val530=
ENST00000689418.1:c.*3662G>C (RAF1) ENSP00000509467.1:n.*3662G>C
ENST00000689540.1:n.4135G>C (RAF1)
ENST00000689876.1:c.*316G>C (RAF1) ENSP00000508535.1:n.*316G>C
ENST00000689914.1:c.*701G>C (RAF1) ENSP00000509847.1:n.*701G>C
ENST00000690397.1:c.1656G>C (RAF1) ENSP00000508730.1:p.Val552=
ENST00000690460.1:c.1755G>C (RAF1) ENSP00000509106.1:p.Val585=
ENST00000690585.1:c.493G>C (RAF1)
ENST00000690625.1:n.2803G>C (RAF1)
ENST00000691396.1:c.*1639G>C (RAF1) ENSP00000510712.1:n.*1639G>C
ENST00000691643.1:n.2820G>C (RAF1)
ENST00000691724.1:c.*724G>C (RAF1) ENSP00000509255.1:n.*724G>C
ENST00000691779.1:c.*1345G>C (RAF1) ENSP00000508592.1:n.*1345G>C
ENST00000691888.1:c.641G>C (RAF1)
ENST00000691899.1:c.1767G>C (RAF1) ENSP00000508763.1:p.Val589=
ENST00000692069.1:n.4691G>C (RAF1)
ENST00000692093.1:c.1668G>C (RAF1) ENSP00000509669.1:p.Val556=
ENST00000692311.1:n.2591G>C (RAF1)
ENST00000692558.1:n.4350G>C (RAF1)
ENST00000692773.1:c.*1504G>C (RAF1) ENSP00000509055.1:n.*1504G>C
ENST00000692830.1:c.*1512G>C (RAF1) ENSP00000509461.1:n.*1512G>C
ENST00000693312.1:c.1542G>C (RAF1) ENSP00000508686.1:p.Val514=
ENST00000693664.1:c.*218G>C (RAF1) ENSP00000509614.1:n.*218G>C
ENST00000693705.1:c.*1146G>C (RAF1) ENSP00000510697.1:n.*1146G>C
ENST00000251849.9:c.1767G>C (RAF1) MANE Select ENSP00000251849.4:p.Val589=
ENST00000442415.7:c.1827G>C (RAF1) ENSP00000401888.2:p.Val609=
ENST00000676541.1:c.*2630C>G (MKRN2) ENSP00000503730.1:n.*2630C>G
ENST00000677142.1:c.*2630C>G (MKRN2) ENSP00000504455.1:n.*2630C>G
ENST00000677816.1:c.*1185C>G (MKRN2) ENSP00000502893.1:n.*1185C>G
ENST00000677941.1:n.2693C>G (MKRN2)
ENST00000251849.8:c.1767G>C (RAF1) ENSP00000251849.4:p.Val589=
ENST00000423275.5:c.*1444G>C (RAF1) ENSP00000401088.1:n.*1444G>C
ENST00000432427.2:c.1404G>C (RAF1) ENSP00000398591.2:p.Val468=
ENST00000442415.6:c.1827G>C (RAF1) ENSP00000401888.2:p.Val609=
ENST00000471449.1:n.456G>C (RAF1)
NM_002880.3:c.1767G>C , LRG_413t1:c.1767G>C (RAF1) NP_002871.1:p.Val589=
XM_005265355.1:c.1767G>C (RAF1) XP_005265412.1:p.Val589=
XM_005265357.1:c.1668G>C (RAF1) XP_005265414.1:p.Val556=
XM_005265358.3:c.1524G>C (RAF1) XP_005265415.1:p.Val508=
XM_005265359.3:c.1425G>C (RAF1) XP_005265416.1:p.Val475=
XM_011533974.1:c.1767G>C (RAF1) XP_011532276.1:p.Val589=
XM_011533975.1:c.1524G>C (RAF1) XP_011532277.1:p.Val508=
NM_001354689.1:c.1827G>C (RAF1) NP_001341618.1:p.Val609=
NM_001354690.1:c.1767G>C (RAF1) NP_001341619.1:p.Val589=
NM_001354691.1:c.1524G>C (RAF1) NP_001341620.1:p.Val508=
NM_001354692.1:c.1524G>C (RAF1) NP_001341621.1:p.Val508=
NM_001354693.1:c.1668G>C (RAF1) NP_001341622.1:p.Val556=
NM_001354694.1:c.1584G>C (RAF1) NP_001341623.1:p.Val528=
NM_001354695.1:c.1425G>C (RAF1) NP_001341624.1:p.Val475=
NR_148940.1:n.2295G>C (RAF1)
NR_148941.1:n.2241G>C (RAF1)
NR_148942.1:n.2180G>C (RAF1)
XM_011533974.3:c.1767G>C (RAF1) XP_011532276.1:p.Val589=
XM_017006966.1:c.1668G>C (RAF1) XP_016862455.1:p.Val556=
NM_001354689.3:c.1827G>C (RAF1) NP_001341618.1:p.Val609=
NM_001354690.2:c.1767G>C (RAF1) NP_001341619.1:p.Val589=
NM_001354691.2:c.1524G>C (RAF1) NP_001341620.1:p.Val508=
NM_001354692.2:c.1524G>C (RAF1) NP_001341621.1:p.Val508=
NM_001354693.2:c.1668G>C (RAF1) NP_001341622.1:p.Val556=
NM_001354694.2:c.1584G>C (RAF1) NP_001341623.1:p.Val528=
NM_001354695.2:c.1425G>C (RAF1) NP_001341624.1:p.Val475=
NR_148940.2:n.2211G>C (RAF1)
NR_148941.2:n.2157G>C (RAF1)
NR_148942.2:n.2096G>C (RAF1)
NM_001354690.3:c.1767G>C (RAF1) NP_001341619.1:p.Val589=
NM_001354691.3:c.1524G>C (RAF1) NP_001341620.1:p.Val508=
NM_001354692.3:c.1524G>C (RAF1) NP_001341621.1:p.Val508=
NM_001354693.3:c.1668G>C (RAF1) NP_001341622.1:p.Val556=
NM_001354694.3:c.1584G>C (RAF1) NP_001341623.1:p.Val528=
NM_001354695.3:c.1425G>C (RAF1) NP_001341624.1:p.Val475=
NM_002880.4:c.1767G>C (RAF1) MANE Select NP_002871.1:p.Val589=
NR_148940.3:n.2211G>C (RAF1)
NR_148941.3:n.2157G>C (RAF1)
NR_148942.3:n.2096G>C (RAF1)