MyVariant.info:
GRCh37
chr3:g.12627264A>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12585765A>T , CM000665.2:g.12585765A>T | GRCh38 |
| NC_000003.11:g.12627264A>T , CM000665.1:g.12627264A>T | GRCh37 |
| NC_000003.10:g.12602264A>T | NCBI36 |
| NG_007467.1:g.83415T>A , LRG_413:g.83415T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1117T>A (RAF1) | ENSP00000401088.1:n.*1117T>A | |
| ENST00000432427.3:c.769T>A (RAF1) | ||
| ENST00000460610.2:n.5197T>A (RAF1) | ||
| ENST00000471449.2:n.262T>A (RAF1) | ||
| ENST00000475353.2:n.3165T>A (RAF1) | ||
| ENST00000684903.1:c.*1129T>A (RAF1) | ENSP00000508612.1:n.*1129T>A | |
| ENST00000685348.1:c.*1095-359T>A (RAF1) | ENSP00000510285.1:n.*1095-359T>A | |
| ENST00000685437.1:c.1353T>A (RAF1) | ENSP00000508794.1:p.Ile451= | |
| ENST00000685653.1:c.1452T>A (RAF1) | ENSP00000509968.1:p.Ile484= | |
| ENST00000685697.1:n.2187T>A (RAF1) | ||
| ENST00000685738.1:c.*416T>A (RAF1) | ENSP00000510156.1:n.*416T>A | |
| ENST00000686409.1:n.4294T>A (RAF1) | ||
| ENST00000686455.1:n.3606T>A (RAF1) | ||
| ENST00000686762.1:c.*11T>A (RAF1) | ENSP00000509767.1:n.*11T>A | |
| ENST00000687257.1:n.3479T>A (RAF1) | ||
| ENST00000687326.1:c.*2177T>A (RAF1) | ENSP00000509665.1:n.*2177T>A | |
| ENST00000687505.1:n.1570T>A (RAF1) | ||
| ENST00000687923.1:c.1341T>A (RAF1) | ENSP00000510255.1:p.Ile447= | |
| ENST00000688269.1:n.2048T>A (RAF1) | ||
| ENST00000688444.1:n.3569T>A (RAF1) | ||
| ENST00000688543.1:c.1353T>A (RAF1) | ENSP00000509612.1:p.Ile451= | |
| ENST00000688625.1:c.*2821T>A (RAF1) | ENSP00000509522.1:n.*2821T>A | |
| ENST00000688803.1:n.2964+510T>A (RAF1) | ||
| ENST00000688914.1:n.438T>A (RAF1) | ||
| ENST00000689097.1:c.*1129T>A (RAF1) | ENSP00000509756.1:n.*1129T>A | |
| ENST00000689389.1:c.1275T>A (RAF1) | ENSP00000510213.1:p.Ile425= | |
| ENST00000689418.1:c.*2920T>A (RAF1) | ENSP00000509467.1:n.*2920T>A | |
| ENST00000689540.1:n.3393T>A (RAF1) | ||
| ENST00000689876.1:c.1418-359T>A (RAF1) | ENSP00000508535.1:n.1418-359T>A | |
| ENST00000689914.1:c.*386T>A (RAF1) | ENSP00000509847.1:n.*386T>A | |
| ENST00000690397.1:c.1341T>A (RAF1) | ENSP00000508730.1:p.Ile447= | |
| ENST00000690460.1:c.1440T>A (RAF1) | ENSP00000509106.1:p.Ile480= | |
| ENST00000690585.1:c.263-512T>A (RAF1) | ||
| ENST00000690625.1:n.2488T>A (RAF1) | ||
| ENST00000691396.1:c.*1324T>A (RAF1) | ENSP00000510712.1:n.*1324T>A | |
| ENST00000691643.1:n.2078T>A (RAF1) | ||
| ENST00000691724.1:c.*409T>A (RAF1) | ENSP00000509255.1:n.*409T>A | |
| ENST00000691779.1:c.*1030T>A (RAF1) | ENSP00000508592.1:n.*1030T>A | |
| ENST00000691888.1:c.326T>A (RAF1) | ||
| ENST00000691899.1:c.1452T>A (RAF1) | ENSP00000508763.1:p.Ile484= | |
| ENST00000692069.1:n.3809T>A (RAF1) | ||
| ENST00000692093.1:c.1353T>A (RAF1) | ENSP00000509669.1:p.Ile451= | |
| ENST00000692311.1:n.2276T>A (RAF1) | ||
| ENST00000692558.1:n.3608T>A (RAF1) | ||
| ENST00000692773.1:c.*1189T>A (RAF1) | ENSP00000509055.1:n.*1189T>A | |
| ENST00000692830.1:c.*1197T>A (RAF1) | ENSP00000509461.1:n.*1197T>A | |
| ENST00000693312.1:c.1227T>A (RAF1) | ENSP00000508686.1:p.Ile409= | |
| ENST00000693664.1:c.1487+510T>A (RAF1) | ENSP00000509614.1:n.1487+510T>A | |
| ENST00000693705.1:c.*1048-784T>A (RAF1) | ENSP00000510697.1:n.*1048-784T>A | |
| ENST00000251849.9:c.1452T>A (RAF1) MANE Select | ENSP00000251849.4:p.Ile484= | |
| ENST00000442415.7:c.1512T>A (RAF1) | ENSP00000401888.2:p.Ile504= | |
| ENST00000676541.1:c.*3512A>T (MKRN2) | ENSP00000503730.1:n.*3512A>T | |
| ENST00000677142.1:c.*3512A>T (MKRN2) | ENSP00000504455.1:n.*3512A>T | |
| ENST00000677816.1:c.*2067A>T (MKRN2) | ENSP00000502893.1:n.*2067A>T | |
| ENST00000677941.1:n.3575A>T (MKRN2) | ||
| ENST00000251849.8:c.1452T>A (RAF1) | ENSP00000251849.4:p.Ile484= | |
| ENST00000423275.5:c.*1129T>A (RAF1) | ENSP00000401088.1:n.*1129T>A | |
| ENST00000432427.2:c.1089T>A (RAF1) | ENSP00000398591.2:p.Ile363= | |
| ENST00000442415.6:c.1512T>A (RAF1) | ENSP00000401888.2:p.Ile504= | |
| ENST00000471449.1:n.141T>A (RAF1) | ||
| NM_002880.3:c.1452T>A , LRG_413t1:c.1452T>A (RAF1) | NP_002871.1:p.Ile484= | |
| XM_005265355.1:c.1452T>A (RAF1) | XP_005265412.1:p.Ile484= | |
| XM_005265357.1:c.1353T>A (RAF1) | XP_005265414.1:p.Ile451= | |
| XM_005265358.3:c.1209T>A (RAF1) | XP_005265415.1:p.Ile403= | |
| XM_005265359.3:c.1110T>A (RAF1) | XP_005265416.1:p.Ile370= | |
| XM_005265360.1:c.1418-359T>A (RAF1) | XP_005265417.1:n.1418-359T>A | |
| XM_011533974.1:c.1452T>A (RAF1) | XP_011532276.1:p.Ile484= | |
| XM_011533975.1:c.1209T>A (RAF1) | XP_011532277.1:p.Ile403= | |
| NM_001354689.1:c.1512T>A (RAF1) | NP_001341618.1:p.Ile504= | |
| NM_001354690.1:c.1452T>A (RAF1) | NP_001341619.1:p.Ile484= | |
| NM_001354691.1:c.1209T>A (RAF1) | NP_001341620.1:p.Ile403= | |
| NM_001354692.1:c.1209T>A (RAF1) | NP_001341621.1:p.Ile403= | |
| NM_001354693.1:c.1353T>A (RAF1) | NP_001341622.1:p.Ile451= | |
| NM_001354694.1:c.1269T>A (RAF1) | NP_001341623.1:p.Ile423= | |
| NM_001354695.1:c.1110T>A (RAF1) | NP_001341624.1:p.Ile370= | |
| NR_148940.1:n.1980T>A (RAF1) | ||
| NR_148941.1:n.1926T>A (RAF1) | ||
| NR_148942.1:n.1865T>A (RAF1) | ||
| XM_011533974.3:c.1452T>A (RAF1) | XP_011532276.1:p.Ile484= | |
| XM_017006966.1:c.1353T>A (RAF1) | XP_016862455.1:p.Ile451= | |
| NM_001354689.3:c.1512T>A (RAF1) | NP_001341618.1:p.Ile504= | |
| NM_001354690.2:c.1452T>A (RAF1) | NP_001341619.1:p.Ile484= | |
| NM_001354691.2:c.1209T>A (RAF1) | NP_001341620.1:p.Ile403= | |
| NM_001354692.2:c.1209T>A (RAF1) | NP_001341621.1:p.Ile403= | |
| NM_001354693.2:c.1353T>A (RAF1) | NP_001341622.1:p.Ile451= | |
| NM_001354694.2:c.1269T>A (RAF1) | NP_001341623.1:p.Ile423= | |
| NM_001354695.2:c.1110T>A (RAF1) | NP_001341624.1:p.Ile370= | |
| NR_148940.2:n.1896T>A (RAF1) | ||
| NR_148941.2:n.1842T>A (RAF1) | ||
| NR_148942.2:n.1781T>A (RAF1) | ||
| NM_001354690.3:c.1452T>A (RAF1) | NP_001341619.1:p.Ile484= | |
| NM_001354691.3:c.1209T>A (RAF1) | NP_001341620.1:p.Ile403= | |
| NM_001354692.3:c.1209T>A (RAF1) | NP_001341621.1:p.Ile403= | |
| NM_001354693.3:c.1353T>A (RAF1) | NP_001341622.1:p.Ile451= | |
| NM_001354694.3:c.1269T>A (RAF1) | NP_001341623.1:p.Ile423= | |
| NM_001354695.3:c.1110T>A (RAF1) | NP_001341624.1:p.Ile370= | |
| NM_002880.4:c.1452T>A (RAF1) MANE Select | NP_002871.1:p.Ile484= | |
| NR_148940.3:n.1896T>A (RAF1) | ||
| NR_148941.3:n.1842T>A (RAF1) | ||
| NR_148942.3:n.1781T>A (RAF1) |