Canonical Allele Identifier: CA432272614

Linked Data

dbSNP Id: rs2125315709
MyVariant Identifiers: chr3:g.12626025C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584526C>T , CM000665.2:g.12584526C>T GRCh38
NC_000003.11:g.12626025C>T , CM000665.1:g.12626025C>T GRCh37
NC_000003.10:g.12601025C>T NCBI36
NG_007467.1:g.84654G>A , LRG_413:g.84654G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1600G>A (RAF1) ENSP00000401088.1:n.*1600G>A
ENST00000432427.3:c.1252G>A (RAF1)
ENST00000460610.2:n.6247G>A (RAF1)
ENST00000471449.2:n.745G>A (RAF1)
ENST00000475353.2:n.4215G>A (RAF1)
ENST00000684903.1:c.*1612G>A (RAF1) ENSP00000508612.1:n.*1612G>A
ENST00000685348.1:c.*1646G>A (RAF1) ENSP00000510285.1:n.*1646G>A
ENST00000685437.1:c.1836G>A (RAF1) ENSP00000508794.1:p.Leu612=
ENST00000685653.1:c.1935G>A (RAF1) ENSP00000509968.1:p.Leu645=
ENST00000685697.1:n.2670G>A (RAF1)
ENST00000685738.1:c.*899G>A (RAF1) ENSP00000510156.1:n.*899G>A
ENST00000686409.1:n.5344G>A (RAF1)
ENST00000686455.1:n.4656G>A (RAF1)
ENST00000686762.1:c.*494G>A (RAF1) ENSP00000509767.1:n.*494G>A
ENST00000687257.1:n.4389G>A (RAF1)
ENST00000687326.1:c.*3227G>A (RAF1) ENSP00000509665.1:n.*3227G>A
ENST00000687505.1:n.2053G>A (RAF1)
ENST00000687923.1:c.1824G>A (RAF1) ENSP00000510255.1:p.Leu608=
ENST00000688269.1:n.2531G>A (RAF1)
ENST00000688444.1:n.4052G>A (RAF1)
ENST00000688543.1:c.1836G>A (RAF1) ENSP00000509612.1:p.Leu612=
ENST00000688625.1:c.*3304G>A (RAF1) ENSP00000509522.1:n.*3304G>A
ENST00000688803.1:n.3363G>A (RAF1)
ENST00000689097.1:c.*1612G>A (RAF1) ENSP00000509756.1:n.*1612G>A
ENST00000689389.1:c.1758G>A (RAF1) ENSP00000510213.1:p.Leu586=
ENST00000689418.1:c.*3830G>A (RAF1) ENSP00000509467.1:n.*3830G>A
ENST00000689540.1:n.4303G>A (RAF1)
ENST00000689876.1:c.*484G>A (RAF1) ENSP00000508535.1:n.*484G>A
ENST00000689914.1:c.*869G>A (RAF1) ENSP00000509847.1:n.*869G>A
ENST00000690397.1:c.1824G>A (RAF1) ENSP00000508730.1:p.Leu608=
ENST00000690460.1:c.1923G>A (RAF1) ENSP00000509106.1:p.Leu641=
ENST00000690585.1:c.661G>A (RAF1)
ENST00000690625.1:n.2971G>A (RAF1)
ENST00000691396.1:c.*1807G>A (RAF1) ENSP00000510712.1:n.*1807G>A
ENST00000691643.1:n.2988G>A (RAF1)
ENST00000691724.1:c.*892G>A (RAF1) ENSP00000509255.1:n.*892G>A
ENST00000691779.1:c.*1513G>A (RAF1) ENSP00000508592.1:n.*1513G>A
ENST00000691888.1:c.809G>A (RAF1)
ENST00000691899.1:c.1935G>A (RAF1) ENSP00000508763.1:p.Leu645=
ENST00000692069.1:n.4859G>A (RAF1)
ENST00000692093.1:c.1836G>A (RAF1) ENSP00000509669.1:p.Leu612=
ENST00000692311.1:n.2759G>A (RAF1)
ENST00000692558.1:n.4518G>A (RAF1)
ENST00000692773.1:c.*1672G>A (RAF1) ENSP00000509055.1:n.*1672G>A
ENST00000692830.1:c.*1680G>A (RAF1) ENSP00000509461.1:n.*1680G>A
ENST00000693312.1:c.1710G>A (RAF1) ENSP00000508686.1:p.Leu570=
ENST00000693664.1:c.*386G>A (RAF1) ENSP00000509614.1:n.*386G>A
ENST00000693705.1:c.*1314G>A (RAF1) ENSP00000510697.1:n.*1314G>A
ENST00000251849.9:c.1935G>A (RAF1) MANE Select ENSP00000251849.4:p.Leu645=
ENST00000442415.7:c.1995G>A (RAF1) ENSP00000401888.2:p.Leu665=
ENST00000676541.1:c.*2273C>T (MKRN2) ENSP00000503730.1:n.*2273C>T
ENST00000677142.1:c.*2273C>T (MKRN2) ENSP00000504455.1:n.*2273C>T
ENST00000677816.1:c.*828C>T (MKRN2) ENSP00000502893.1:n.*828C>T
ENST00000677941.1:n.2336C>T (MKRN2)
ENST00000251849.8:c.1935G>A (RAF1) ENSP00000251849.4:p.Leu645=
ENST00000423275.5:c.*1612G>A (RAF1) ENSP00000401088.1:n.*1612G>A
ENST00000432427.2:c.1572G>A (RAF1) ENSP00000398591.2:p.Leu524=
ENST00000442415.6:c.1995G>A (RAF1) ENSP00000401888.2:p.Leu665=
ENST00000471449.1:n.624G>A (RAF1)
NM_002880.3:c.1935G>A , LRG_413t1:c.1935G>A (RAF1) NP_002871.1:p.Leu645=
XM_005265355.1:c.1935G>A (RAF1) XP_005265412.1:p.Leu645=
XM_005265357.1:c.1836G>A (RAF1) XP_005265414.1:p.Leu612=
XM_005265358.3:c.1692G>A (RAF1) XP_005265415.1:p.Leu564=
XM_005265359.3:c.1593G>A (RAF1) XP_005265416.1:p.Leu531=
XM_011533974.1:c.1935G>A (RAF1) XP_011532276.1:p.Leu645=
XM_011533975.1:c.1692G>A (RAF1) XP_011532277.1:p.Leu564=
NM_001354689.1:c.1995G>A (RAF1) NP_001341618.1:p.Leu665=
NM_001354690.1:c.1935G>A (RAF1) NP_001341619.1:p.Leu645=
NM_001354691.1:c.1692G>A (RAF1) NP_001341620.1:p.Leu564=
NM_001354692.1:c.1692G>A (RAF1) NP_001341621.1:p.Leu564=
NM_001354693.1:c.1836G>A (RAF1) NP_001341622.1:p.Leu612=
NM_001354694.1:c.1752G>A (RAF1) NP_001341623.1:p.Leu584=
NM_001354695.1:c.1593G>A (RAF1) NP_001341624.1:p.Leu531=
NR_148940.1:n.2463G>A (RAF1)
NR_148941.1:n.2409G>A (RAF1)
NR_148942.1:n.2348G>A (RAF1)
XM_011533974.3:c.1935G>A (RAF1) XP_011532276.1:p.Leu645=
XM_017006966.1:c.1836G>A (RAF1) XP_016862455.1:p.Leu612=
NM_001354689.3:c.1995G>A (RAF1) NP_001341618.1:p.Leu665=
NM_001354690.2:c.1935G>A (RAF1) NP_001341619.1:p.Leu645=
NM_001354691.2:c.1692G>A (RAF1) NP_001341620.1:p.Leu564=
NM_001354692.2:c.1692G>A (RAF1) NP_001341621.1:p.Leu564=
NM_001354693.2:c.1836G>A (RAF1) NP_001341622.1:p.Leu612=
NM_001354694.2:c.1752G>A (RAF1) NP_001341623.1:p.Leu584=
NM_001354695.2:c.1593G>A (RAF1) NP_001341624.1:p.Leu531=
NR_148940.2:n.2379G>A (RAF1)
NR_148941.2:n.2325G>A (RAF1)
NR_148942.2:n.2264G>A (RAF1)
NM_001354690.3:c.1935G>A (RAF1) NP_001341619.1:p.Leu645=
NM_001354691.3:c.1692G>A (RAF1) NP_001341620.1:p.Leu564=
NM_001354692.3:c.1692G>A (RAF1) NP_001341621.1:p.Leu564=
NM_001354693.3:c.1836G>A (RAF1) NP_001341622.1:p.Leu612=
NM_001354694.3:c.1752G>A (RAF1) NP_001341623.1:p.Leu584=
NM_001354695.3:c.1593G>A (RAF1) NP_001341624.1:p.Leu531=
NM_002880.4:c.1935G>A (RAF1) MANE Select NP_002871.1:p.Leu645=
NR_148940.3:n.2379G>A (RAF1)
NR_148941.3:n.2325G>A (RAF1)
NR_148942.3:n.2264G>A (RAF1)