MyVariant.info:
GRCh37
chr3:g.12627255A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12585756A>G , CM000665.2:g.12585756A>G | GRCh38 |
| NC_000003.11:g.12627255A>G , CM000665.1:g.12627255A>G | GRCh37 |
| NC_000003.10:g.12602255A>G | NCBI36 |
| NG_007467.1:g.83424T>C , LRG_413:g.83424T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1126T>C (RAF1) | ENSP00000401088.1:n.*1126T>C | |
| ENST00000432427.3:c.778T>C (RAF1) | ||
| ENST00000460610.2:n.5206T>C (RAF1) | ||
| ENST00000471449.2:n.271T>C (RAF1) | ||
| ENST00000475353.2:n.3174T>C (RAF1) | ||
| ENST00000684903.1:c.*1138T>C (RAF1) | ENSP00000508612.1:n.*1138T>C | |
| ENST00000685348.1:c.*1095-350T>C (RAF1) | ENSP00000510285.1:n.*1095-350T>C | |
| ENST00000685437.1:c.1362T>C (RAF1) | ENSP00000508794.1:p.Phe454= | |
| ENST00000685653.1:c.1461T>C (RAF1) | ENSP00000509968.1:p.Phe487= | |
| ENST00000685697.1:n.2196T>C (RAF1) | ||
| ENST00000685738.1:c.*425T>C (RAF1) | ENSP00000510156.1:n.*425T>C | |
| ENST00000686409.1:n.4303T>C (RAF1) | ||
| ENST00000686455.1:n.3615T>C (RAF1) | ||
| ENST00000686762.1:c.*20T>C (RAF1) | ENSP00000509767.1:n.*20T>C | |
| ENST00000687257.1:n.3488T>C (RAF1) | ||
| ENST00000687326.1:c.*2186T>C (RAF1) | ENSP00000509665.1:n.*2186T>C | |
| ENST00000687505.1:n.1579T>C (RAF1) | ||
| ENST00000687923.1:c.1350T>C (RAF1) | ENSP00000510255.1:p.Phe450= | |
| ENST00000688269.1:n.2057T>C (RAF1) | ||
| ENST00000688444.1:n.3578T>C (RAF1) | ||
| ENST00000688543.1:c.1362T>C (RAF1) | ENSP00000509612.1:p.Phe454= | |
| ENST00000688625.1:c.*2830T>C (RAF1) | ENSP00000509522.1:n.*2830T>C | |
| ENST00000688803.1:n.2965-503T>C (RAF1) | ||
| ENST00000688914.1:n.447T>C (RAF1) | ||
| ENST00000689097.1:c.*1138T>C (RAF1) | ENSP00000509756.1:n.*1138T>C | |
| ENST00000689389.1:c.1284T>C (RAF1) | ENSP00000510213.1:p.Phe428= | |
| ENST00000689418.1:c.*2929T>C (RAF1) | ENSP00000509467.1:n.*2929T>C | |
| ENST00000689540.1:n.3402T>C (RAF1) | ||
| ENST00000689876.1:c.1418-350T>C (RAF1) | ENSP00000508535.1:n.1418-350T>C | |
| ENST00000689914.1:c.*395T>C (RAF1) | ENSP00000509847.1:n.*395T>C | |
| ENST00000690397.1:c.1350T>C (RAF1) | ENSP00000508730.1:p.Phe450= | |
| ENST00000690460.1:c.1449T>C (RAF1) | ENSP00000509106.1:p.Phe483= | |
| ENST00000690585.1:c.263-503T>C (RAF1) | ||
| ENST00000690625.1:n.2497T>C (RAF1) | ||
| ENST00000691396.1:c.*1333T>C (RAF1) | ENSP00000510712.1:n.*1333T>C | |
| ENST00000691643.1:n.2087T>C (RAF1) | ||
| ENST00000691724.1:c.*418T>C (RAF1) | ENSP00000509255.1:n.*418T>C | |
| ENST00000691779.1:c.*1039T>C (RAF1) | ENSP00000508592.1:n.*1039T>C | |
| ENST00000691888.1:c.335T>C (RAF1) | ||
| ENST00000691899.1:c.1461T>C (RAF1) | ENSP00000508763.1:p.Phe487= | |
| ENST00000692069.1:n.3818T>C (RAF1) | ||
| ENST00000692093.1:c.1362T>C (RAF1) | ENSP00000509669.1:p.Phe454= | |
| ENST00000692311.1:n.2285T>C (RAF1) | ||
| ENST00000692558.1:n.3617T>C (RAF1) | ||
| ENST00000692773.1:c.*1198T>C (RAF1) | ENSP00000509055.1:n.*1198T>C | |
| ENST00000692830.1:c.*1206T>C (RAF1) | ENSP00000509461.1:n.*1206T>C | |
| ENST00000693312.1:c.1236T>C (RAF1) | ENSP00000508686.1:p.Phe412= | |
| ENST00000693664.1:c.1488-503T>C (RAF1) | ENSP00000509614.1:n.1488-503T>C | |
| ENST00000693705.1:c.*1048-775T>C (RAF1) | ENSP00000510697.1:n.*1048-775T>C | |
| ENST00000251849.9:c.1461T>C (RAF1) MANE Select | ENSP00000251849.4:p.Phe487= | |
| ENST00000442415.7:c.1521T>C (RAF1) | ENSP00000401888.2:p.Phe507= | |
| ENST00000676541.1:c.*3503A>G (MKRN2) | ENSP00000503730.1:n.*3503A>G | |
| ENST00000677142.1:c.*3503A>G (MKRN2) | ENSP00000504455.1:n.*3503A>G | |
| ENST00000677816.1:c.*2058A>G (MKRN2) | ENSP00000502893.1:n.*2058A>G | |
| ENST00000677941.1:n.3566A>G (MKRN2) | ||
| ENST00000251849.8:c.1461T>C (RAF1) | ENSP00000251849.4:p.Phe487= | |
| ENST00000423275.5:c.*1138T>C (RAF1) | ENSP00000401088.1:n.*1138T>C | |
| ENST00000432427.2:c.1098T>C (RAF1) | ENSP00000398591.2:p.Phe366= | |
| ENST00000442415.6:c.1521T>C (RAF1) | ENSP00000401888.2:p.Phe507= | |
| ENST00000471449.1:n.150T>C (RAF1) | ||
| NM_002880.3:c.1461T>C , LRG_413t1:c.1461T>C (RAF1) | NP_002871.1:p.Phe487= | |
| XM_005265355.1:c.1461T>C (RAF1) | XP_005265412.1:p.Phe487= | |
| XM_005265357.1:c.1362T>C (RAF1) | XP_005265414.1:p.Phe454= | |
| XM_005265358.3:c.1218T>C (RAF1) | XP_005265415.1:p.Phe406= | |
| XM_005265359.3:c.1119T>C (RAF1) | XP_005265416.1:p.Phe373= | |
| XM_005265360.1:c.1418-350T>C (RAF1) | XP_005265417.1:n.1418-350T>C | |
| XM_011533974.1:c.1461T>C (RAF1) | XP_011532276.1:p.Phe487= | |
| XM_011533975.1:c.1218T>C (RAF1) | XP_011532277.1:p.Phe406= | |
| NM_001354689.1:c.1521T>C (RAF1) | NP_001341618.1:p.Phe507= | |
| NM_001354690.1:c.1461T>C (RAF1) | NP_001341619.1:p.Phe487= | |
| NM_001354691.1:c.1218T>C (RAF1) | NP_001341620.1:p.Phe406= | |
| NM_001354692.1:c.1218T>C (RAF1) | NP_001341621.1:p.Phe406= | |
| NM_001354693.1:c.1362T>C (RAF1) | NP_001341622.1:p.Phe454= | |
| NM_001354694.1:c.1278T>C (RAF1) | NP_001341623.1:p.Phe426= | |
| NM_001354695.1:c.1119T>C (RAF1) | NP_001341624.1:p.Phe373= | |
| NR_148940.1:n.1989T>C (RAF1) | ||
| NR_148941.1:n.1935T>C (RAF1) | ||
| NR_148942.1:n.1874T>C (RAF1) | ||
| XM_011533974.3:c.1461T>C (RAF1) | XP_011532276.1:p.Phe487= | |
| XM_017006966.1:c.1362T>C (RAF1) | XP_016862455.1:p.Phe454= | |
| NM_001354689.3:c.1521T>C (RAF1) | NP_001341618.1:p.Phe507= | |
| NM_001354690.2:c.1461T>C (RAF1) | NP_001341619.1:p.Phe487= | |
| NM_001354691.2:c.1218T>C (RAF1) | NP_001341620.1:p.Phe406= | |
| NM_001354692.2:c.1218T>C (RAF1) | NP_001341621.1:p.Phe406= | |
| NM_001354693.2:c.1362T>C (RAF1) | NP_001341622.1:p.Phe454= | |
| NM_001354694.2:c.1278T>C (RAF1) | NP_001341623.1:p.Phe426= | |
| NM_001354695.2:c.1119T>C (RAF1) | NP_001341624.1:p.Phe373= | |
| NR_148940.2:n.1905T>C (RAF1) | ||
| NR_148941.2:n.1851T>C (RAF1) | ||
| NR_148942.2:n.1790T>C (RAF1) | ||
| NM_001354690.3:c.1461T>C (RAF1) | NP_001341619.1:p.Phe487= | |
| NM_001354691.3:c.1218T>C (RAF1) | NP_001341620.1:p.Phe406= | |
| NM_001354692.3:c.1218T>C (RAF1) | NP_001341621.1:p.Phe406= | |
| NM_001354693.3:c.1362T>C (RAF1) | NP_001341622.1:p.Phe454= | |
| NM_001354694.3:c.1278T>C (RAF1) | NP_001341623.1:p.Phe426= | |
| NM_001354695.3:c.1119T>C (RAF1) | NP_001341624.1:p.Phe373= | |
| NM_002880.4:c.1461T>C (RAF1) MANE Select | NP_002871.1:p.Phe487= | |
| NR_148940.3:n.1905T>C (RAF1) | ||
| NR_148941.3:n.1851T>C (RAF1) | ||
| NR_148942.3:n.1790T>C (RAF1) |