MyVariant.info:
GRCh37
chr3:g.12626027G>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12584528G>A , CM000665.2:g.12584528G>A | GRCh38 |
| NC_000003.11:g.12626027G>A , CM000665.1:g.12626027G>A | GRCh37 |
| NC_000003.10:g.12601027G>A | NCBI36 |
| NG_007467.1:g.84652C>T , LRG_413:g.84652C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1598C>T (RAF1) | ENSP00000401088.1:n.*1598C>T | |
| ENST00000432427.3:c.1250C>T (RAF1) | ||
| ENST00000460610.2:n.6245C>T (RAF1) | ||
| ENST00000471449.2:n.743C>T (RAF1) | ||
| ENST00000475353.2:n.4213C>T (RAF1) | ||
| ENST00000684903.1:c.*1610C>T (RAF1) | ENSP00000508612.1:n.*1610C>T | |
| ENST00000685348.1:c.*1644C>T (RAF1) | ENSP00000510285.1:n.*1644C>T | |
| ENST00000685437.1:c.1834C>T (RAF1) | ENSP00000508794.1:p.Leu612= | |
| ENST00000685653.1:c.1933C>T (RAF1) | ENSP00000509968.1:p.Leu645= | |
| ENST00000685697.1:n.2668C>T (RAF1) | ||
| ENST00000685738.1:c.*897C>T (RAF1) | ENSP00000510156.1:n.*897C>T | |
| ENST00000686409.1:n.5342C>T (RAF1) | ||
| ENST00000686455.1:n.4654C>T (RAF1) | ||
| ENST00000686762.1:c.*492C>T (RAF1) | ENSP00000509767.1:n.*492C>T | |
| ENST00000687257.1:n.4387C>T (RAF1) | ||
| ENST00000687326.1:c.*3225C>T (RAF1) | ENSP00000509665.1:n.*3225C>T | |
| ENST00000687505.1:n.2051C>T (RAF1) | ||
| ENST00000687923.1:c.1822C>T (RAF1) | ENSP00000510255.1:p.Leu608= | |
| ENST00000688269.1:n.2529C>T (RAF1) | ||
| ENST00000688444.1:n.4050C>T (RAF1) | ||
| ENST00000688543.1:c.1834C>T (RAF1) | ENSP00000509612.1:p.Leu612= | |
| ENST00000688625.1:c.*3302C>T (RAF1) | ENSP00000509522.1:n.*3302C>T | |
| ENST00000688803.1:n.3361C>T (RAF1) | ||
| ENST00000689097.1:c.*1610C>T (RAF1) | ENSP00000509756.1:n.*1610C>T | |
| ENST00000689389.1:c.1756C>T (RAF1) | ENSP00000510213.1:p.Leu586= | |
| ENST00000689418.1:c.*3828C>T (RAF1) | ENSP00000509467.1:n.*3828C>T | |
| ENST00000689540.1:n.4301C>T (RAF1) | ||
| ENST00000689876.1:c.*482C>T (RAF1) | ENSP00000508535.1:n.*482C>T | |
| ENST00000689914.1:c.*867C>T (RAF1) | ENSP00000509847.1:n.*867C>T | |
| ENST00000690397.1:c.1822C>T (RAF1) | ENSP00000508730.1:p.Leu608= | |
| ENST00000690460.1:c.1921C>T (RAF1) | ENSP00000509106.1:p.Leu641= | |
| ENST00000690585.1:c.659C>T (RAF1) | ||
| ENST00000690625.1:n.2969C>T (RAF1) | ||
| ENST00000691396.1:c.*1805C>T (RAF1) | ENSP00000510712.1:n.*1805C>T | |
| ENST00000691643.1:n.2986C>T (RAF1) | ||
| ENST00000691724.1:c.*890C>T (RAF1) | ENSP00000509255.1:n.*890C>T | |
| ENST00000691779.1:c.*1511C>T (RAF1) | ENSP00000508592.1:n.*1511C>T | |
| ENST00000691888.1:c.807C>T (RAF1) | ||
| ENST00000691899.1:c.1933C>T (RAF1) | ENSP00000508763.1:p.Leu645= | |
| ENST00000692069.1:n.4857C>T (RAF1) | ||
| ENST00000692093.1:c.1834C>T (RAF1) | ENSP00000509669.1:p.Leu612= | |
| ENST00000692311.1:n.2757C>T (RAF1) | ||
| ENST00000692558.1:n.4516C>T (RAF1) | ||
| ENST00000692773.1:c.*1670C>T (RAF1) | ENSP00000509055.1:n.*1670C>T | |
| ENST00000692830.1:c.*1678C>T (RAF1) | ENSP00000509461.1:n.*1678C>T | |
| ENST00000693312.1:c.1708C>T (RAF1) | ENSP00000508686.1:p.Leu570= | |
| ENST00000693664.1:c.*384C>T (RAF1) | ENSP00000509614.1:n.*384C>T | |
| ENST00000693705.1:c.*1312C>T (RAF1) | ENSP00000510697.1:n.*1312C>T | |
| ENST00000251849.9:c.1933C>T (RAF1) MANE Select | ENSP00000251849.4:p.Leu645= | |
| ENST00000442415.7:c.1993C>T (RAF1) | ENSP00000401888.2:p.Leu665= | |
| ENST00000676541.1:c.*2275G>A (MKRN2) | ENSP00000503730.1:n.*2275G>A | |
| ENST00000677142.1:c.*2275G>A (MKRN2) | ENSP00000504455.1:n.*2275G>A | |
| ENST00000677816.1:c.*830G>A (MKRN2) | ENSP00000502893.1:n.*830G>A | |
| ENST00000677941.1:n.2338G>A (MKRN2) | ||
| ENST00000251849.8:c.1933C>T (RAF1) | ENSP00000251849.4:p.Leu645= | |
| ENST00000423275.5:c.*1610C>T (RAF1) | ENSP00000401088.1:n.*1610C>T | |
| ENST00000432427.2:c.1570C>T (RAF1) | ENSP00000398591.2:p.Leu524= | |
| ENST00000442415.6:c.1993C>T (RAF1) | ENSP00000401888.2:p.Leu665= | |
| ENST00000471449.1:n.622C>T (RAF1) | ||
| NM_002880.3:c.1933C>T , LRG_413t1:c.1933C>T (RAF1) | NP_002871.1:p.Leu645= | |
| XM_005265355.1:c.1933C>T (RAF1) | XP_005265412.1:p.Leu645= | |
| XM_005265357.1:c.1834C>T (RAF1) | XP_005265414.1:p.Leu612= | |
| XM_005265358.3:c.1690C>T (RAF1) | XP_005265415.1:p.Leu564= | |
| XM_005265359.3:c.1591C>T (RAF1) | XP_005265416.1:p.Leu531= | |
| XM_011533974.1:c.1933C>T (RAF1) | XP_011532276.1:p.Leu645= | |
| XM_011533975.1:c.1690C>T (RAF1) | XP_011532277.1:p.Leu564= | |
| NM_001354689.1:c.1993C>T (RAF1) | NP_001341618.1:p.Leu665= | |
| NM_001354690.1:c.1933C>T (RAF1) | NP_001341619.1:p.Leu645= | |
| NM_001354691.1:c.1690C>T (RAF1) | NP_001341620.1:p.Leu564= | |
| NM_001354692.1:c.1690C>T (RAF1) | NP_001341621.1:p.Leu564= | |
| NM_001354693.1:c.1834C>T (RAF1) | NP_001341622.1:p.Leu612= | |
| NM_001354694.1:c.1750C>T (RAF1) | NP_001341623.1:p.Leu584= | |
| NM_001354695.1:c.1591C>T (RAF1) | NP_001341624.1:p.Leu531= | |
| NR_148940.1:n.2461C>T (RAF1) | ||
| NR_148941.1:n.2407C>T (RAF1) | ||
| NR_148942.1:n.2346C>T (RAF1) | ||
| XM_011533974.3:c.1933C>T (RAF1) | XP_011532276.1:p.Leu645= | |
| XM_017006966.1:c.1834C>T (RAF1) | XP_016862455.1:p.Leu612= | |
| NM_001354689.3:c.1993C>T (RAF1) | NP_001341618.1:p.Leu665= | |
| NM_001354690.2:c.1933C>T (RAF1) | NP_001341619.1:p.Leu645= | |
| NM_001354691.2:c.1690C>T (RAF1) | NP_001341620.1:p.Leu564= | |
| NM_001354692.2:c.1690C>T (RAF1) | NP_001341621.1:p.Leu564= | |
| NM_001354693.2:c.1834C>T (RAF1) | NP_001341622.1:p.Leu612= | |
| NM_001354694.2:c.1750C>T (RAF1) | NP_001341623.1:p.Leu584= | |
| NM_001354695.2:c.1591C>T (RAF1) | NP_001341624.1:p.Leu531= | |
| NR_148940.2:n.2377C>T (RAF1) | ||
| NR_148941.2:n.2323C>T (RAF1) | ||
| NR_148942.2:n.2262C>T (RAF1) | ||
| NM_001354690.3:c.1933C>T (RAF1) | NP_001341619.1:p.Leu645= | |
| NM_001354691.3:c.1690C>T (RAF1) | NP_001341620.1:p.Leu564= | |
| NM_001354692.3:c.1690C>T (RAF1) | NP_001341621.1:p.Leu564= | |
| NM_001354693.3:c.1834C>T (RAF1) | NP_001341622.1:p.Leu612= | |
| NM_001354694.3:c.1750C>T (RAF1) | NP_001341623.1:p.Leu584= | |
| NM_001354695.3:c.1591C>T (RAF1) | NP_001341624.1:p.Leu531= | |
| NM_002880.4:c.1933C>T (RAF1) MANE Select | NP_002871.1:p.Leu645= | |
| NR_148940.3:n.2377C>T (RAF1) | ||
| NR_148941.3:n.2323C>T (RAF1) | ||
| NR_148942.3:n.2262C>T (RAF1) |