Canonical Allele Identifier: CA3012390332
Gene: RAF1 HGNC NCBI
MKRN2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12583790A>C , CM000665.2:g.12583790A>C GRCh38
NC_000003.11:g.12625289A>C , CM000665.1:g.12625289A>C GRCh37
NC_000003.10:g.12600289A>C NCBI36
NG_007467.1:g.85390T>G , LRG_413:g.85390T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*2336T>G (RAF1) ENSP00000401088.1:n.*2336T>G
ENST00000432427.3:c.1988T>G (RAF1)
ENST00000460610.2:n.6983T>G (RAF1)
ENST00000471449.2:n.1481T>G (RAF1)
ENST00000475353.2:n.4951T>G (RAF1)
ENST00000684903.1:c.*2348T>G (RAF1) ENSP00000508612.1:n.*2348T>G
ENST00000685348.1:c.*2382T>G (RAF1) ENSP00000510285.1:n.*2382T>G
ENST00000685653.1:c.*724T>G (RAF1) ENSP00000509968.1:n.*724T>G
ENST00000685697.1:n.3406T>G (RAF1)
ENST00000685738.1:c.*1635T>G (RAF1) ENSP00000510156.1:n.*1635T>G
ENST00000686409.1:n.6080T>G (RAF1)
ENST00000686455.1:n.5392T>G (RAF1)
ENST00000686762.1:c.*1230T>G (RAF1) ENSP00000509767.1:n.*1230T>G
ENST00000687257.1:n.5125T>G (RAF1)
ENST00000687326.1:c.*3963T>G (RAF1) ENSP00000509665.1:n.*3963T>G
ENST00000687923.1:c.*724T>G (RAF1) ENSP00000510255.1:n.*724T>G
ENST00000688269.1:n.3267T>G (RAF1)
ENST00000688444.1:n.4788T>G (RAF1)
ENST00000688543.1:c.*724T>G (RAF1) ENSP00000509612.1:n.*724T>G
ENST00000688625.1:c.*4040T>G (RAF1) ENSP00000509522.1:n.*4040T>G
ENST00000688803.1:n.4099T>G (RAF1)
ENST00000689097.1:c.*2348T>G (RAF1) ENSP00000509756.1:n.*2348T>G
ENST00000689389.1:c.*724T>G (RAF1) ENSP00000510213.1:n.*724T>G
ENST00000689540.1:n.5039T>G (RAF1)
ENST00000689876.1:c.*1220T>G (RAF1) ENSP00000508535.1:n.*1220T>G
ENST00000689914.1:c.*1605T>G (RAF1) ENSP00000509847.1:n.*1605T>G
ENST00000690397.1:c.*724T>G (RAF1) ENSP00000508730.1:n.*724T>G
ENST00000690460.1:c.*724T>G (RAF1) ENSP00000509106.1:n.*724T>G
ENST00000690585.1:c.1397T>G (RAF1)
ENST00000690625.1:n.3707T>G (RAF1)
ENST00000691643.1:n.3724T>G (RAF1)
ENST00000691724.1:c.*1628T>G (RAF1) ENSP00000509255.1:n.*1628T>G
ENST00000691779.1:c.*2249T>G (RAF1) ENSP00000508592.1:n.*2249T>G
ENST00000691888.1:c.1545T>G (RAF1)
ENST00000691899.1:c.*724T>G (RAF1) ENSP00000508763.1:n.*724T>G
ENST00000692069.1:n.5595T>G (RAF1)
ENST00000692093.1:c.*724T>G (RAF1) ENSP00000509669.1:n.*724T>G
ENST00000692311.1:n.3495T>G (RAF1)
ENST00000692558.1:n.5254T>G (RAF1)
ENST00000692773.1:c.*2408T>G (RAF1) ENSP00000509055.1:n.*2408T>G
ENST00000692830.1:c.*2416T>G (RAF1) ENSP00000509461.1:n.*2416T>G
ENST00000693312.1:c.*724T>G (RAF1) ENSP00000508686.1:n.*724T>G
ENST00000693664.1:c.*1122T>G (RAF1) ENSP00000509614.1:n.*1122T>G
ENST00000693705.1:c.*2050T>G (RAF1) ENSP00000510697.1:n.*2050T>G
ENST00000251849.9:c.*724T>G (RAF1) MANE Select ENSP00000251849.4:n.*724T>G
ENST00000442415.7:c.*724T>G (RAF1) ENSP00000401888.2:n.*724T>G
ENST00000676541.1:c.*1537A>C (MKRN2) ENSP00000503730.1:n.*1537A>C
ENST00000677142.1:c.*1537A>C (MKRN2) ENSP00000504455.1:n.*1537A>C
ENST00000677816.1:c.*92A>C (MKRN2) ENSP00000502893.1:n.*92A>C
ENST00000677941.1:n.1600A>C (MKRN2)
ENST00000251849.8:c.*724T>G (RAF1) ENSP00000251849.4:n.*724T>G
NM_002880.3:c.*724T>G , LRG_413t1:c.*724T>G (RAF1) NP_002871.1:n.*724T>G
XM_005265355.1:c.*724T>G (RAF1) XP_005265412.1:n.*724T>G
XM_005265357.1:c.*724T>G (RAF1) XP_005265414.1:n.*724T>G
XM_005265358.3:c.*724T>G (RAF1) XP_005265415.1:n.*724T>G
XM_005265359.3:c.*724T>G (RAF1) XP_005265416.1:n.*724T>G
XM_011533974.1:c.*724T>G (RAF1) XP_011532276.1:n.*724T>G
XM_011533975.1:c.*724T>G (RAF1) XP_011532277.1:n.*724T>G
NM_001354689.1:c.*724T>G (RAF1) NP_001341618.1:n.*724T>G
NM_001354690.1:c.*724T>G (RAF1) NP_001341619.1:n.*724T>G
NM_001354691.1:c.*724T>G (RAF1) NP_001341620.1:n.*724T>G
NM_001354692.1:c.*724T>G (RAF1) NP_001341621.1:n.*724T>G
NM_001354693.1:c.*724T>G (RAF1) NP_001341622.1:n.*724T>G
NM_001354694.1:c.*724T>G (RAF1) NP_001341623.1:n.*724T>G
NM_001354695.1:c.*724T>G (RAF1) NP_001341624.1:n.*724T>G
NR_148940.1:n.3199T>G (RAF1)
NR_148941.1:n.3145T>G (RAF1)
NR_148942.1:n.3084T>G (RAF1)
XM_011533974.3:c.*724T>G (RAF1) XP_011532276.1:n.*724T>G
XM_017006966.1:c.*724T>G (RAF1) XP_016862455.1:n.*724T>G
NM_001354689.3:c.*724T>G (RAF1) NP_001341618.1:n.*724T>G
NM_001354690.2:c.*724T>G (RAF1) NP_001341619.1:n.*724T>G
NM_001354691.2:c.*724T>G (RAF1) NP_001341620.1:n.*724T>G
NM_001354692.2:c.*724T>G (RAF1) NP_001341621.1:n.*724T>G
NM_001354693.2:c.*724T>G (RAF1) NP_001341622.1:n.*724T>G
NM_001354694.2:c.*724T>G (RAF1) NP_001341623.1:n.*724T>G
NM_001354695.2:c.*724T>G (RAF1) NP_001341624.1:n.*724T>G
NR_148940.2:n.3115T>G (RAF1)
NR_148941.2:n.3061T>G (RAF1)
NR_148942.2:n.3000T>G (RAF1)
NM_001354690.3:c.*724T>G (RAF1) NP_001341619.1:n.*724T>G
NM_001354691.3:c.*724T>G (RAF1) NP_001341620.1:n.*724T>G
NM_001354692.3:c.*724T>G (RAF1) NP_001341621.1:n.*724T>G
NM_001354693.3:c.*724T>G (RAF1) NP_001341622.1:n.*724T>G
NM_001354694.3:c.*724T>G (RAF1) NP_001341623.1:n.*724T>G
NM_001354695.3:c.*724T>G (RAF1) NP_001341624.1:n.*724T>G
NM_002880.4:c.*724T>G (RAF1) MANE Select NP_002871.1:n.*724T>G
NR_148940.3:n.3115T>G (RAF1)
NR_148941.3:n.3061T>G (RAF1)
NR_148942.3:n.3000T>G (RAF1)
Search 100 bp 5'
Search 100 bp 3'