Canonical Allele Identifier: CA351496545

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584873T>A , CM000665.2:g.12584873T>A GRCh38
NC_000003.11:g.12626372T>A , CM000665.1:g.12626372T>A GRCh37
NC_000003.10:g.12601372T>A NCBI36
NG_007467.1:g.84307A>T , LRG_413:g.84307A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1442A>T (RAF1) ENSP00000401088.1:n.*1442A>T
ENST00000432427.3:c.1094A>T (RAF1)
ENST00000460610.2:n.6089A>T (RAF1)
ENST00000471449.2:n.587A>T (RAF1)
ENST00000475353.2:n.4057A>T (RAF1)
ENST00000684903.1:c.*1454A>T (RAF1) ENSP00000508612.1:n.*1454A>T
ENST00000685348.1:c.*1488A>T (RAF1) ENSP00000510285.1:n.*1488A>T
ENST00000685437.1:c.1678A>T (RAF1) ENSP00000508794.1:p.Lys560Ter
ENST00000685653.1:c.1777A>T (RAF1) ENSP00000509968.1:p.Lys593Ter
ENST00000685697.1:n.2512A>T (RAF1)
ENST00000685738.1:c.*741A>T (RAF1) ENSP00000510156.1:n.*741A>T
ENST00000686409.1:n.5186A>T (RAF1)
ENST00000686455.1:n.4498A>T (RAF1)
ENST00000686762.1:c.*336A>T (RAF1) ENSP00000509767.1:n.*336A>T
ENST00000687257.1:n.4231A>T (RAF1)
ENST00000687326.1:c.*3069A>T (RAF1) ENSP00000509665.1:n.*3069A>T
ENST00000687505.1:n.1895A>T (RAF1)
ENST00000687923.1:c.1666A>T (RAF1) ENSP00000510255.1:p.Lys556Ter
ENST00000688269.1:n.2373A>T (RAF1)
ENST00000688444.1:n.3894A>T (RAF1)
ENST00000688543.1:c.1678A>T (RAF1) ENSP00000509612.1:p.Lys560Ter
ENST00000688625.1:c.*3146A>T (RAF1) ENSP00000509522.1:n.*3146A>T
ENST00000688803.1:n.3205A>T (RAF1)
ENST00000689097.1:c.*1454A>T (RAF1) ENSP00000509756.1:n.*1454A>T
ENST00000689389.1:c.1600A>T (RAF1) ENSP00000510213.1:p.Lys534Ter
ENST00000689418.1:c.*3672A>T (RAF1) ENSP00000509467.1:n.*3672A>T
ENST00000689540.1:n.4145A>T (RAF1)
ENST00000689876.1:c.*326A>T (RAF1) ENSP00000508535.1:n.*326A>T
ENST00000689914.1:c.*711A>T (RAF1) ENSP00000509847.1:n.*711A>T
ENST00000690397.1:c.1666A>T (RAF1) ENSP00000508730.1:p.Lys556Ter
ENST00000690460.1:c.1765A>T (RAF1) ENSP00000509106.1:p.Lys589Ter
ENST00000690585.1:c.503A>T (RAF1)
ENST00000690625.1:n.2813A>T (RAF1)
ENST00000691396.1:c.*1649A>T (RAF1) ENSP00000510712.1:n.*1649A>T
ENST00000691643.1:n.2830A>T (RAF1)
ENST00000691724.1:c.*734A>T (RAF1) ENSP00000509255.1:n.*734A>T
ENST00000691779.1:c.*1355A>T (RAF1) ENSP00000508592.1:n.*1355A>T
ENST00000691888.1:c.651A>T (RAF1)
ENST00000691899.1:c.1777A>T (RAF1) ENSP00000508763.1:p.Lys593Ter
ENST00000692069.1:n.4701A>T (RAF1)
ENST00000692093.1:c.1678A>T (RAF1) ENSP00000509669.1:p.Lys560Ter
ENST00000692311.1:n.2601A>T (RAF1)
ENST00000692558.1:n.4360A>T (RAF1)
ENST00000692773.1:c.*1514A>T (RAF1) ENSP00000509055.1:n.*1514A>T
ENST00000692830.1:c.*1522A>T (RAF1) ENSP00000509461.1:n.*1522A>T
ENST00000693312.1:c.1552A>T (RAF1) ENSP00000508686.1:p.Lys518Ter
ENST00000693664.1:c.*228A>T (RAF1) ENSP00000509614.1:n.*228A>T
ENST00000693705.1:c.*1156A>T (RAF1) ENSP00000510697.1:n.*1156A>T
ENST00000251849.9:c.1777A>T (RAF1) MANE Select ENSP00000251849.4:p.Lys593Ter
ENST00000442415.7:c.1837A>T (RAF1) ENSP00000401888.2:p.Lys613Ter
ENST00000676541.1:c.*2620T>A (MKRN2) ENSP00000503730.1:n.*2620T>A
ENST00000677142.1:c.*2620T>A (MKRN2) ENSP00000504455.1:n.*2620T>A
ENST00000677816.1:c.*1175T>A (MKRN2) ENSP00000502893.1:n.*1175T>A
ENST00000677941.1:n.2683T>A (MKRN2)
ENST00000251849.8:c.1777A>T (RAF1) ENSP00000251849.4:p.Lys593Ter
ENST00000423275.5:c.*1454A>T (RAF1) ENSP00000401088.1:n.*1454A>T
ENST00000432427.2:c.1414A>T (RAF1) ENSP00000398591.2:p.Lys472Ter
ENST00000442415.6:c.1837A>T (RAF1) ENSP00000401888.2:p.Lys613Ter
ENST00000471449.1:n.466A>T (RAF1)
NM_002880.3:c.1777A>T , LRG_413t1:c.1777A>T (RAF1) NP_002871.1:p.Lys593Ter
XM_005265355.1:c.1777A>T (RAF1) XP_005265412.1:p.Lys593Ter
XM_005265357.1:c.1678A>T (RAF1) XP_005265414.1:p.Lys560Ter
XM_005265358.3:c.1534A>T (RAF1) XP_005265415.1:p.Lys512Ter
XM_005265359.3:c.1435A>T (RAF1) XP_005265416.1:p.Lys479Ter
XM_011533974.1:c.1777A>T (RAF1) XP_011532276.1:p.Lys593Ter
XM_011533975.1:c.1534A>T (RAF1) XP_011532277.1:p.Lys512Ter
NM_001354689.1:c.1837A>T (RAF1) NP_001341618.1:p.Lys613Ter
NM_001354690.1:c.1777A>T (RAF1) NP_001341619.1:p.Lys593Ter
NM_001354691.1:c.1534A>T (RAF1) NP_001341620.1:p.Lys512Ter
NM_001354692.1:c.1534A>T (RAF1) NP_001341621.1:p.Lys512Ter
NM_001354693.1:c.1678A>T (RAF1) NP_001341622.1:p.Lys560Ter
NM_001354694.1:c.1594A>T (RAF1) NP_001341623.1:p.Lys532Ter
NM_001354695.1:c.1435A>T (RAF1) NP_001341624.1:p.Lys479Ter
NR_148940.1:n.2305A>T (RAF1)
NR_148941.1:n.2251A>T (RAF1)
NR_148942.1:n.2190A>T (RAF1)
XM_011533974.3:c.1777A>T (RAF1) XP_011532276.1:p.Lys593Ter
XM_017006966.1:c.1678A>T (RAF1) XP_016862455.1:p.Lys560Ter
NM_001354689.3:c.1837A>T (RAF1) NP_001341618.1:p.Lys613Ter
NM_001354690.2:c.1777A>T (RAF1) NP_001341619.1:p.Lys593Ter
NM_001354691.2:c.1534A>T (RAF1) NP_001341620.1:p.Lys512Ter
NM_001354692.2:c.1534A>T (RAF1) NP_001341621.1:p.Lys512Ter
NM_001354693.2:c.1678A>T (RAF1) NP_001341622.1:p.Lys560Ter
NM_001354694.2:c.1594A>T (RAF1) NP_001341623.1:p.Lys532Ter
NM_001354695.2:c.1435A>T (RAF1) NP_001341624.1:p.Lys479Ter
NR_148940.2:n.2221A>T (RAF1)
NR_148941.2:n.2167A>T (RAF1)
NR_148942.2:n.2106A>T (RAF1)
NM_001354690.3:c.1777A>T (RAF1) NP_001341619.1:p.Lys593Ter
NM_001354691.3:c.1534A>T (RAF1) NP_001341620.1:p.Lys512Ter
NM_001354692.3:c.1534A>T (RAF1) NP_001341621.1:p.Lys512Ter
NM_001354693.3:c.1678A>T (RAF1) NP_001341622.1:p.Lys560Ter
NM_001354694.3:c.1594A>T (RAF1) NP_001341623.1:p.Lys532Ter
NM_001354695.3:c.1435A>T (RAF1) NP_001341624.1:p.Lys479Ter
NM_002880.4:c.1777A>T (RAF1) MANE Select NP_002871.1:p.Lys593Ter
NR_148940.3:n.2221A>T (RAF1)
NR_148941.3:n.2167A>T (RAF1)
NR_148942.3:n.2106A>T (RAF1)