MyVariant.info:
GRCh37
chr3:g.12626028C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12584529C>T , CM000665.2:g.12584529C>T | GRCh38 |
| NC_000003.11:g.12626028C>T , CM000665.1:g.12626028C>T | GRCh37 |
| NC_000003.10:g.12601028C>T | NCBI36 |
| NG_007467.1:g.84651G>A , LRG_413:g.84651G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1597G>A (RAF1) | ENSP00000401088.1:n.*1597G>A | |
| ENST00000432427.3:c.1249G>A (RAF1) | ||
| ENST00000460610.2:n.6244G>A (RAF1) | ||
| ENST00000471449.2:n.742G>A (RAF1) | ||
| ENST00000475353.2:n.4212G>A (RAF1) | ||
| ENST00000684903.1:c.*1609G>A (RAF1) | ENSP00000508612.1:n.*1609G>A | |
| ENST00000685348.1:c.*1643G>A (RAF1) | ENSP00000510285.1:n.*1643G>A | |
| ENST00000685437.1:c.1833G>A (RAF1) | ENSP00000508794.1:p.Arg611= | |
| ENST00000685653.1:c.1932G>A (RAF1) | ENSP00000509968.1:p.Arg644= | |
| ENST00000685697.1:n.2667G>A (RAF1) | ||
| ENST00000685738.1:c.*896G>A (RAF1) | ENSP00000510156.1:n.*896G>A | |
| ENST00000686409.1:n.5341G>A (RAF1) | ||
| ENST00000686455.1:n.4653G>A (RAF1) | ||
| ENST00000686762.1:c.*491G>A (RAF1) | ENSP00000509767.1:n.*491G>A | |
| ENST00000687257.1:n.4386G>A (RAF1) | ||
| ENST00000687326.1:c.*3224G>A (RAF1) | ENSP00000509665.1:n.*3224G>A | |
| ENST00000687505.1:n.2050G>A (RAF1) | ||
| ENST00000687923.1:c.1821G>A (RAF1) | ENSP00000510255.1:p.Arg607= | |
| ENST00000688269.1:n.2528G>A (RAF1) | ||
| ENST00000688444.1:n.4049G>A (RAF1) | ||
| ENST00000688543.1:c.1833G>A (RAF1) | ENSP00000509612.1:p.Arg611= | |
| ENST00000688625.1:c.*3301G>A (RAF1) | ENSP00000509522.1:n.*3301G>A | |
| ENST00000688803.1:n.3360G>A (RAF1) | ||
| ENST00000689097.1:c.*1609G>A (RAF1) | ENSP00000509756.1:n.*1609G>A | |
| ENST00000689389.1:c.1755G>A (RAF1) | ENSP00000510213.1:p.Arg585= | |
| ENST00000689418.1:c.*3827G>A (RAF1) | ENSP00000509467.1:n.*3827G>A | |
| ENST00000689540.1:n.4300G>A (RAF1) | ||
| ENST00000689876.1:c.*481G>A (RAF1) | ENSP00000508535.1:n.*481G>A | |
| ENST00000689914.1:c.*866G>A (RAF1) | ENSP00000509847.1:n.*866G>A | |
| ENST00000690397.1:c.1821G>A (RAF1) | ENSP00000508730.1:p.Arg607= | |
| ENST00000690460.1:c.1920G>A (RAF1) | ENSP00000509106.1:p.Arg640= | |
| ENST00000690585.1:c.658G>A (RAF1) | ||
| ENST00000690625.1:n.2968G>A (RAF1) | ||
| ENST00000691396.1:c.*1804G>A (RAF1) | ENSP00000510712.1:n.*1804G>A | |
| ENST00000691643.1:n.2985G>A (RAF1) | ||
| ENST00000691724.1:c.*889G>A (RAF1) | ENSP00000509255.1:n.*889G>A | |
| ENST00000691779.1:c.*1510G>A (RAF1) | ENSP00000508592.1:n.*1510G>A | |
| ENST00000691888.1:c.806G>A (RAF1) | ||
| ENST00000691899.1:c.1932G>A (RAF1) | ENSP00000508763.1:p.Arg644= | |
| ENST00000692069.1:n.4856G>A (RAF1) | ||
| ENST00000692093.1:c.1833G>A (RAF1) | ENSP00000509669.1:p.Arg611= | |
| ENST00000692311.1:n.2756G>A (RAF1) | ||
| ENST00000692558.1:n.4515G>A (RAF1) | ||
| ENST00000692773.1:c.*1669G>A (RAF1) | ENSP00000509055.1:n.*1669G>A | |
| ENST00000692830.1:c.*1677G>A (RAF1) | ENSP00000509461.1:n.*1677G>A | |
| ENST00000693312.1:c.1707G>A (RAF1) | ENSP00000508686.1:p.Arg569= | |
| ENST00000693664.1:c.*383G>A (RAF1) | ENSP00000509614.1:n.*383G>A | |
| ENST00000693705.1:c.*1311G>A (RAF1) | ENSP00000510697.1:n.*1311G>A | |
| ENST00000251849.9:c.1932G>A (RAF1) MANE Select | ENSP00000251849.4:p.Arg644= | |
| ENST00000442415.7:c.1992G>A (RAF1) | ENSP00000401888.2:p.Arg664= | |
| ENST00000676541.1:c.*2276C>T (MKRN2) | ENSP00000503730.1:n.*2276C>T | |
| ENST00000677142.1:c.*2276C>T (MKRN2) | ENSP00000504455.1:n.*2276C>T | |
| ENST00000677816.1:c.*831C>T (MKRN2) | ENSP00000502893.1:n.*831C>T | |
| ENST00000677941.1:n.2339C>T (MKRN2) | ||
| ENST00000251849.8:c.1932G>A (RAF1) | ENSP00000251849.4:p.Arg644= | |
| ENST00000423275.5:c.*1609G>A (RAF1) | ENSP00000401088.1:n.*1609G>A | |
| ENST00000432427.2:c.1569G>A (RAF1) | ENSP00000398591.2:p.Arg523= | |
| ENST00000442415.6:c.1992G>A (RAF1) | ENSP00000401888.2:p.Arg664= | |
| ENST00000471449.1:n.621G>A (RAF1) | ||
| NM_002880.3:c.1932G>A , LRG_413t1:c.1932G>A (RAF1) | NP_002871.1:p.Arg644= | |
| XM_005265355.1:c.1932G>A (RAF1) | XP_005265412.1:p.Arg644= | |
| XM_005265357.1:c.1833G>A (RAF1) | XP_005265414.1:p.Arg611= | |
| XM_005265358.3:c.1689G>A (RAF1) | XP_005265415.1:p.Arg563= | |
| XM_005265359.3:c.1590G>A (RAF1) | XP_005265416.1:p.Arg530= | |
| XM_011533974.1:c.1932G>A (RAF1) | XP_011532276.1:p.Arg644= | |
| XM_011533975.1:c.1689G>A (RAF1) | XP_011532277.1:p.Arg563= | |
| NM_001354689.1:c.1992G>A (RAF1) | NP_001341618.1:p.Arg664= | |
| NM_001354690.1:c.1932G>A (RAF1) | NP_001341619.1:p.Arg644= | |
| NM_001354691.1:c.1689G>A (RAF1) | NP_001341620.1:p.Arg563= | |
| NM_001354692.1:c.1689G>A (RAF1) | NP_001341621.1:p.Arg563= | |
| NM_001354693.1:c.1833G>A (RAF1) | NP_001341622.1:p.Arg611= | |
| NM_001354694.1:c.1749G>A (RAF1) | NP_001341623.1:p.Arg583= | |
| NM_001354695.1:c.1590G>A (RAF1) | NP_001341624.1:p.Arg530= | |
| NR_148940.1:n.2460G>A (RAF1) | ||
| NR_148941.1:n.2406G>A (RAF1) | ||
| NR_148942.1:n.2345G>A (RAF1) | ||
| XM_011533974.3:c.1932G>A (RAF1) | XP_011532276.1:p.Arg644= | |
| XM_017006966.1:c.1833G>A (RAF1) | XP_016862455.1:p.Arg611= | |
| NM_001354689.3:c.1992G>A (RAF1) | NP_001341618.1:p.Arg664= | |
| NM_001354690.2:c.1932G>A (RAF1) | NP_001341619.1:p.Arg644= | |
| NM_001354691.2:c.1689G>A (RAF1) | NP_001341620.1:p.Arg563= | |
| NM_001354692.2:c.1689G>A (RAF1) | NP_001341621.1:p.Arg563= | |
| NM_001354693.2:c.1833G>A (RAF1) | NP_001341622.1:p.Arg611= | |
| NM_001354694.2:c.1749G>A (RAF1) | NP_001341623.1:p.Arg583= | |
| NM_001354695.2:c.1590G>A (RAF1) | NP_001341624.1:p.Arg530= | |
| NR_148940.2:n.2376G>A (RAF1) | ||
| NR_148941.2:n.2322G>A (RAF1) | ||
| NR_148942.2:n.2261G>A (RAF1) | ||
| NM_001354690.3:c.1932G>A (RAF1) | NP_001341619.1:p.Arg644= | |
| NM_001354691.3:c.1689G>A (RAF1) | NP_001341620.1:p.Arg563= | |
| NM_001354692.3:c.1689G>A (RAF1) | NP_001341621.1:p.Arg563= | |
| NM_001354693.3:c.1833G>A (RAF1) | NP_001341622.1:p.Arg611= | |
| NM_001354694.3:c.1749G>A (RAF1) | NP_001341623.1:p.Arg583= | |
| NM_001354695.3:c.1590G>A (RAF1) | NP_001341624.1:p.Arg530= | |
| NM_002880.4:c.1932G>A (RAF1) MANE Select | NP_002871.1:p.Arg644= | |
| NR_148940.3:n.2376G>A (RAF1) | ||
| NR_148941.3:n.2322G>A (RAF1) | ||
| NR_148942.3:n.2261G>A (RAF1) |