MyVariant.info:
GRCh37
chr3:g.12627273T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12585774T>C , CM000665.2:g.12585774T>C | GRCh38 |
| NC_000003.11:g.12627273T>C , CM000665.1:g.12627273T>C | GRCh37 |
| NC_000003.10:g.12602273T>C | NCBI36 |
| NG_007467.1:g.83406A>G , LRG_413:g.83406A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1108A>G (RAF1) | ENSP00000401088.1:n.*1108A>G | |
| ENST00000432427.3:c.760A>G (RAF1) | ||
| ENST00000460610.2:n.5188A>G (RAF1) | ||
| ENST00000471449.2:n.253A>G (RAF1) | ||
| ENST00000475353.2:n.3156A>G (RAF1) | ||
| ENST00000684903.1:c.*1120A>G (RAF1) | ENSP00000508612.1:n.*1120A>G | |
| ENST00000685348.1:c.*1095-368A>G (RAF1) | ENSP00000510285.1:n.*1095-368A>G | |
| ENST00000685437.1:c.1344A>G (RAF1) | ENSP00000508794.1:p.Thr448= | |
| ENST00000685653.1:c.1443A>G (RAF1) | ENSP00000509968.1:p.Thr481= | |
| ENST00000685697.1:n.2178A>G (RAF1) | ||
| ENST00000685738.1:c.*407A>G (RAF1) | ENSP00000510156.1:n.*407A>G | |
| ENST00000686409.1:n.4285A>G (RAF1) | ||
| ENST00000686455.1:n.3597A>G (RAF1) | ||
| ENST00000686762.1:c.*2A>G (RAF1) | ENSP00000509767.1:n.*2A>G | |
| ENST00000687257.1:n.3470A>G (RAF1) | ||
| ENST00000687326.1:c.*2168A>G (RAF1) | ENSP00000509665.1:n.*2168A>G | |
| ENST00000687505.1:n.1561A>G (RAF1) | ||
| ENST00000687923.1:c.1332A>G (RAF1) | ENSP00000510255.1:p.Thr444= | |
| ENST00000688269.1:n.2039A>G (RAF1) | ||
| ENST00000688444.1:n.3560A>G (RAF1) | ||
| ENST00000688543.1:c.1344A>G (RAF1) | ENSP00000509612.1:p.Thr448= | |
| ENST00000688625.1:c.*2812A>G (RAF1) | ENSP00000509522.1:n.*2812A>G | |
| ENST00000688803.1:n.2964+501A>G (RAF1) | ||
| ENST00000688914.1:n.429A>G (RAF1) | ||
| ENST00000689097.1:c.*1120A>G (RAF1) | ENSP00000509756.1:n.*1120A>G | |
| ENST00000689389.1:c.1266A>G (RAF1) | ENSP00000510213.1:p.Thr422= | |
| ENST00000689418.1:c.*2911A>G (RAF1) | ENSP00000509467.1:n.*2911A>G | |
| ENST00000689540.1:n.3384A>G (RAF1) | ||
| ENST00000689876.1:c.1418-368A>G (RAF1) | ENSP00000508535.1:n.1418-368A>G | |
| ENST00000689914.1:c.*377A>G (RAF1) | ENSP00000509847.1:n.*377A>G | |
| ENST00000690397.1:c.1332A>G (RAF1) | ENSP00000508730.1:p.Thr444= | |
| ENST00000690460.1:c.1431A>G (RAF1) | ENSP00000509106.1:p.Thr477= | |
| ENST00000690585.1:c.263-521A>G (RAF1) | ||
| ENST00000690625.1:n.2479A>G (RAF1) | ||
| ENST00000691396.1:c.*1315A>G (RAF1) | ENSP00000510712.1:n.*1315A>G | |
| ENST00000691643.1:n.2069A>G (RAF1) | ||
| ENST00000691724.1:c.*400A>G (RAF1) | ENSP00000509255.1:n.*400A>G | |
| ENST00000691779.1:c.*1021A>G (RAF1) | ENSP00000508592.1:n.*1021A>G | |
| ENST00000691888.1:c.317A>G (RAF1) | ||
| ENST00000691899.1:c.1443A>G (RAF1) | ENSP00000508763.1:p.Thr481= | |
| ENST00000692069.1:n.3800A>G (RAF1) | ||
| ENST00000692093.1:c.1344A>G (RAF1) | ENSP00000509669.1:p.Thr448= | |
| ENST00000692311.1:n.2267A>G (RAF1) | ||
| ENST00000692558.1:n.3599A>G (RAF1) | ||
| ENST00000692773.1:c.*1180A>G (RAF1) | ENSP00000509055.1:n.*1180A>G | |
| ENST00000692830.1:c.*1188A>G (RAF1) | ENSP00000509461.1:n.*1188A>G | |
| ENST00000693312.1:c.1218A>G (RAF1) | ENSP00000508686.1:p.Thr406= | |
| ENST00000693664.1:c.1487+501A>G (RAF1) | ENSP00000509614.1:n.1487+501A>G | |
| ENST00000693705.1:c.*1048-793A>G (RAF1) | ENSP00000510697.1:n.*1048-793A>G | |
| ENST00000251849.9:c.1443A>G (RAF1) MANE Select | ENSP00000251849.4:p.Thr481= | |
| ENST00000442415.7:c.1503A>G (RAF1) | ENSP00000401888.2:p.Thr501= | |
| ENST00000676541.1:c.*3521T>C (MKRN2) | ENSP00000503730.1:n.*3521T>C | |
| ENST00000677142.1:c.*3521T>C (MKRN2) | ENSP00000504455.1:n.*3521T>C | |
| ENST00000677816.1:c.*2076T>C (MKRN2) | ENSP00000502893.1:n.*2076T>C | |
| ENST00000677941.1:n.3584T>C (MKRN2) | ||
| ENST00000251849.8:c.1443A>G (RAF1) | ENSP00000251849.4:p.Thr481= | |
| ENST00000423275.5:c.*1120A>G (RAF1) | ENSP00000401088.1:n.*1120A>G | |
| ENST00000432427.2:c.1080A>G (RAF1) | ENSP00000398591.2:p.Thr360= | |
| ENST00000442415.6:c.1503A>G (RAF1) | ENSP00000401888.2:p.Thr501= | |
| ENST00000471449.1:n.132A>G (RAF1) | ||
| NM_002880.3:c.1443A>G , LRG_413t1:c.1443A>G (RAF1) | NP_002871.1:p.Thr481= | |
| XM_005265355.1:c.1443A>G (RAF1) | XP_005265412.1:p.Thr481= | |
| XM_005265357.1:c.1344A>G (RAF1) | XP_005265414.1:p.Thr448= | |
| XM_005265358.3:c.1200A>G (RAF1) | XP_005265415.1:p.Thr400= | |
| XM_005265359.3:c.1101A>G (RAF1) | XP_005265416.1:p.Thr367= | |
| XM_005265360.1:c.1418-368A>G (RAF1) | XP_005265417.1:n.1418-368A>G | |
| XM_011533974.1:c.1443A>G (RAF1) | XP_011532276.1:p.Thr481= | |
| XM_011533975.1:c.1200A>G (RAF1) | XP_011532277.1:p.Thr400= | |
| NM_001354689.1:c.1503A>G (RAF1) | NP_001341618.1:p.Thr501= | |
| NM_001354690.1:c.1443A>G (RAF1) | NP_001341619.1:p.Thr481= | |
| NM_001354691.1:c.1200A>G (RAF1) | NP_001341620.1:p.Thr400= | |
| NM_001354692.1:c.1200A>G (RAF1) | NP_001341621.1:p.Thr400= | |
| NM_001354693.1:c.1344A>G (RAF1) | NP_001341622.1:p.Thr448= | |
| NM_001354694.1:c.1260A>G (RAF1) | NP_001341623.1:p.Thr420= | |
| NM_001354695.1:c.1101A>G (RAF1) | NP_001341624.1:p.Thr367= | |
| NR_148940.1:n.1971A>G (RAF1) | ||
| NR_148941.1:n.1917A>G (RAF1) | ||
| NR_148942.1:n.1856A>G (RAF1) | ||
| XM_011533974.3:c.1443A>G (RAF1) | XP_011532276.1:p.Thr481= | |
| XM_017006966.1:c.1344A>G (RAF1) | XP_016862455.1:p.Thr448= | |
| NM_001354689.3:c.1503A>G (RAF1) | NP_001341618.1:p.Thr501= | |
| NM_001354690.2:c.1443A>G (RAF1) | NP_001341619.1:p.Thr481= | |
| NM_001354691.2:c.1200A>G (RAF1) | NP_001341620.1:p.Thr400= | |
| NM_001354692.2:c.1200A>G (RAF1) | NP_001341621.1:p.Thr400= | |
| NM_001354693.2:c.1344A>G (RAF1) | NP_001341622.1:p.Thr448= | |
| NM_001354694.2:c.1260A>G (RAF1) | NP_001341623.1:p.Thr420= | |
| NM_001354695.2:c.1101A>G (RAF1) | NP_001341624.1:p.Thr367= | |
| NR_148940.2:n.1887A>G (RAF1) | ||
| NR_148941.2:n.1833A>G (RAF1) | ||
| NR_148942.2:n.1772A>G (RAF1) | ||
| NM_001354690.3:c.1443A>G (RAF1) | NP_001341619.1:p.Thr481= | |
| NM_001354691.3:c.1200A>G (RAF1) | NP_001341620.1:p.Thr400= | |
| NM_001354692.3:c.1200A>G (RAF1) | NP_001341621.1:p.Thr400= | |
| NM_001354693.3:c.1344A>G (RAF1) | NP_001341622.1:p.Thr448= | |
| NM_001354694.3:c.1260A>G (RAF1) | NP_001341623.1:p.Thr420= | |
| NM_001354695.3:c.1101A>G (RAF1) | NP_001341624.1:p.Thr367= | |
| NM_002880.4:c.1443A>G (RAF1) MANE Select | NP_002871.1:p.Thr481= | |
| NR_148940.3:n.1887A>G (RAF1) | ||
| NR_148941.3:n.1833A>G (RAF1) | ||
| NR_148942.3:n.1772A>G (RAF1) |