Canonical Allele Identifier: CA432522008

Linked Data

MyVariant Identifiers: chr3:g.12626379C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584880C>T , CM000665.2:g.12584880C>T GRCh38
NC_000003.11:g.12626379C>T , CM000665.1:g.12626379C>T GRCh37
NC_000003.10:g.12601379C>T NCBI36
NG_007467.1:g.84300G>A , LRG_413:g.84300G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1435G>A (RAF1) ENSP00000401088.1:n.*1435G>A
ENST00000432427.3:c.1087G>A (RAF1)
ENST00000460610.2:n.6082G>A (RAF1)
ENST00000471449.2:n.580G>A (RAF1)
ENST00000475353.2:n.4050G>A (RAF1)
ENST00000684903.1:c.*1447G>A (RAF1) ENSP00000508612.1:n.*1447G>A
ENST00000685348.1:c.*1481G>A (RAF1) ENSP00000510285.1:n.*1481G>A
ENST00000685437.1:c.1671G>A (RAF1) ENSP00000508794.1:p.Lys557=
ENST00000685653.1:c.1770G>A (RAF1) ENSP00000509968.1:p.Lys590=
ENST00000685697.1:n.2505G>A (RAF1)
ENST00000685738.1:c.*734G>A (RAF1) ENSP00000510156.1:n.*734G>A
ENST00000686409.1:n.5179G>A (RAF1)
ENST00000686455.1:n.4491G>A (RAF1)
ENST00000686762.1:c.*329G>A (RAF1) ENSP00000509767.1:n.*329G>A
ENST00000687257.1:n.4224G>A (RAF1)
ENST00000687326.1:c.*3062G>A (RAF1) ENSP00000509665.1:n.*3062G>A
ENST00000687505.1:n.1888G>A (RAF1)
ENST00000687923.1:c.1659G>A (RAF1) ENSP00000510255.1:p.Lys553=
ENST00000688269.1:n.2366G>A (RAF1)
ENST00000688444.1:n.3887G>A (RAF1)
ENST00000688543.1:c.1671G>A (RAF1) ENSP00000509612.1:p.Lys557=
ENST00000688625.1:c.*3139G>A (RAF1) ENSP00000509522.1:n.*3139G>A
ENST00000688803.1:n.3198G>A (RAF1)
ENST00000689097.1:c.*1447G>A (RAF1) ENSP00000509756.1:n.*1447G>A
ENST00000689389.1:c.1593G>A (RAF1) ENSP00000510213.1:p.Lys531=
ENST00000689418.1:c.*3665G>A (RAF1) ENSP00000509467.1:n.*3665G>A
ENST00000689540.1:n.4138G>A (RAF1)
ENST00000689876.1:c.*319G>A (RAF1) ENSP00000508535.1:n.*319G>A
ENST00000689914.1:c.*704G>A (RAF1) ENSP00000509847.1:n.*704G>A
ENST00000690397.1:c.1659G>A (RAF1) ENSP00000508730.1:p.Lys553=
ENST00000690460.1:c.1758G>A (RAF1) ENSP00000509106.1:p.Lys586=
ENST00000690585.1:c.496G>A (RAF1)
ENST00000690625.1:n.2806G>A (RAF1)
ENST00000691396.1:c.*1642G>A (RAF1) ENSP00000510712.1:n.*1642G>A
ENST00000691643.1:n.2823G>A (RAF1)
ENST00000691724.1:c.*727G>A (RAF1) ENSP00000509255.1:n.*727G>A
ENST00000691779.1:c.*1348G>A (RAF1) ENSP00000508592.1:n.*1348G>A
ENST00000691888.1:c.644G>A (RAF1)
ENST00000691899.1:c.1770G>A (RAF1) ENSP00000508763.1:p.Lys590=
ENST00000692069.1:n.4694G>A (RAF1)
ENST00000692093.1:c.1671G>A (RAF1) ENSP00000509669.1:p.Lys557=
ENST00000692311.1:n.2594G>A (RAF1)
ENST00000692558.1:n.4353G>A (RAF1)
ENST00000692773.1:c.*1507G>A (RAF1) ENSP00000509055.1:n.*1507G>A
ENST00000692830.1:c.*1515G>A (RAF1) ENSP00000509461.1:n.*1515G>A
ENST00000693312.1:c.1545G>A (RAF1) ENSP00000508686.1:p.Lys515=
ENST00000693664.1:c.*221G>A (RAF1) ENSP00000509614.1:n.*221G>A
ENST00000693705.1:c.*1149G>A (RAF1) ENSP00000510697.1:n.*1149G>A
ENST00000251849.9:c.1770G>A (RAF1) MANE Select ENSP00000251849.4:p.Lys590=
ENST00000442415.7:c.1830G>A (RAF1) ENSP00000401888.2:p.Lys610=
ENST00000676541.1:c.*2627C>T (MKRN2) ENSP00000503730.1:n.*2627C>T
ENST00000677142.1:c.*2627C>T (MKRN2) ENSP00000504455.1:n.*2627C>T
ENST00000677816.1:c.*1182C>T (MKRN2) ENSP00000502893.1:n.*1182C>T
ENST00000677941.1:n.2690C>T (MKRN2)
ENST00000251849.8:c.1770G>A (RAF1) ENSP00000251849.4:p.Lys590=
ENST00000423275.5:c.*1447G>A (RAF1) ENSP00000401088.1:n.*1447G>A
ENST00000432427.2:c.1407G>A (RAF1) ENSP00000398591.2:p.Lys469=
ENST00000442415.6:c.1830G>A (RAF1) ENSP00000401888.2:p.Lys610=
ENST00000471449.1:n.459G>A (RAF1)
NM_002880.3:c.1770G>A , LRG_413t1:c.1770G>A (RAF1) NP_002871.1:p.Lys590=
XM_005265355.1:c.1770G>A (RAF1) XP_005265412.1:p.Lys590=
XM_005265357.1:c.1671G>A (RAF1) XP_005265414.1:p.Lys557=
XM_005265358.3:c.1527G>A (RAF1) XP_005265415.1:p.Lys509=
XM_005265359.3:c.1428G>A (RAF1) XP_005265416.1:p.Lys476=
XM_011533974.1:c.1770G>A (RAF1) XP_011532276.1:p.Lys590=
XM_011533975.1:c.1527G>A (RAF1) XP_011532277.1:p.Lys509=
NM_001354689.1:c.1830G>A (RAF1) NP_001341618.1:p.Lys610=
NM_001354690.1:c.1770G>A (RAF1) NP_001341619.1:p.Lys590=
NM_001354691.1:c.1527G>A (RAF1) NP_001341620.1:p.Lys509=
NM_001354692.1:c.1527G>A (RAF1) NP_001341621.1:p.Lys509=
NM_001354693.1:c.1671G>A (RAF1) NP_001341622.1:p.Lys557=
NM_001354694.1:c.1587G>A (RAF1) NP_001341623.1:p.Lys529=
NM_001354695.1:c.1428G>A (RAF1) NP_001341624.1:p.Lys476=
NR_148940.1:n.2298G>A (RAF1)
NR_148941.1:n.2244G>A (RAF1)
NR_148942.1:n.2183G>A (RAF1)
XM_011533974.3:c.1770G>A (RAF1) XP_011532276.1:p.Lys590=
XM_017006966.1:c.1671G>A (RAF1) XP_016862455.1:p.Lys557=
NM_001354689.3:c.1830G>A (RAF1) NP_001341618.1:p.Lys610=
NM_001354690.2:c.1770G>A (RAF1) NP_001341619.1:p.Lys590=
NM_001354691.2:c.1527G>A (RAF1) NP_001341620.1:p.Lys509=
NM_001354692.2:c.1527G>A (RAF1) NP_001341621.1:p.Lys509=
NM_001354693.2:c.1671G>A (RAF1) NP_001341622.1:p.Lys557=
NM_001354694.2:c.1587G>A (RAF1) NP_001341623.1:p.Lys529=
NM_001354695.2:c.1428G>A (RAF1) NP_001341624.1:p.Lys476=
NR_148940.2:n.2214G>A (RAF1)
NR_148941.2:n.2160G>A (RAF1)
NR_148942.2:n.2099G>A (RAF1)
NM_001354690.3:c.1770G>A (RAF1) NP_001341619.1:p.Lys590=
NM_001354691.3:c.1527G>A (RAF1) NP_001341620.1:p.Lys509=
NM_001354692.3:c.1527G>A (RAF1) NP_001341621.1:p.Lys509=
NM_001354693.3:c.1671G>A (RAF1) NP_001341622.1:p.Lys557=
NM_001354694.3:c.1587G>A (RAF1) NP_001341623.1:p.Lys529=
NM_001354695.3:c.1428G>A (RAF1) NP_001341624.1:p.Lys476=
NM_002880.4:c.1770G>A (RAF1) MANE Select NP_002871.1:p.Lys590=
NR_148940.3:n.2214G>A (RAF1)
NR_148941.3:n.2160G>A (RAF1)
NR_148942.3:n.2099G>A (RAF1)