Linked Data
dbSNP Id:
rs772245311
ExAC:
3:12625971 TCTC / T
gnomAD v2:
3-12625971-TCTC-T
gnomAD v3:
3-12584472-TCTC-T
gnomAD v4:
3-12584472-TCTC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12584480_12584482del , CM000665.2:g.12584480_12584482del | GRCh38 |
| NC_000003.11:g.12625979_12625981del , CM000665.1:g.12625979_12625981del | GRCh37 |
| NC_000003.10:g.12600979_12600981del | NCBI36 |
| NG_007467.1:g.84705_84707del , LRG_413:g.84705_84707del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1651_*1653del (RAF1) | ENSP00000401088.1:n.*1651_*1653del | |
| ENST00000432427.3:c.1303_1305del (RAF1) | ||
| ENST00000460610.2:n.6298_6300del (RAF1) | ||
| ENST00000471449.2:n.796_798del (RAF1) | ||
| ENST00000475353.2:n.4266_4268del (RAF1) | ||
| ENST00000684903.1:c.*1663_*1665del (RAF1) | ENSP00000508612.1:n.*1663_*1665del | |
| ENST00000685348.1:c.*1697_*1699del (RAF1) | ENSP00000510285.1:n.*1697_*1699del | |
| ENST00000685437.1:c.*39_*41del (RAF1) | ENSP00000508794.1:n.*39_*41del | |
| ENST00000685653.1:c.*39_*41del (RAF1) | ENSP00000509968.1:n.*39_*41del | |
| ENST00000685697.1:n.2721_2723del (RAF1) | ||
| ENST00000685738.1:c.*950_*952del (RAF1) | ENSP00000510156.1:n.*950_*952del | |
| ENST00000686409.1:n.5395_5397del (RAF1) | ||
| ENST00000686455.1:n.4707_4709del (RAF1) | ||
| ENST00000686762.1:c.*545_*547del (RAF1) | ENSP00000509767.1:n.*545_*547del | |
| ENST00000687257.1:n.4440_4442del (RAF1) | ||
| ENST00000687326.1:c.*3278_*3280del (RAF1) | ENSP00000509665.1:n.*3278_*3280del | |
| ENST00000687505.1:n.2104_2106del (RAF1) | ||
| ENST00000687923.1:c.*39_*41del (RAF1) | ENSP00000510255.1:n.*39_*41del | |
| ENST00000688269.1:n.2582_2584del (RAF1) | ||
| ENST00000688444.1:n.4103_4105del (RAF1) | ||
| ENST00000688543.1:c.*39_*41del (RAF1) | ENSP00000509612.1:n.*39_*41del | |
| ENST00000688625.1:c.*3355_*3357del (RAF1) | ENSP00000509522.1:n.*3355_*3357del | |
| ENST00000688803.1:n.3414_3416del (RAF1) | ||
| ENST00000689097.1:c.*1663_*1665del (RAF1) | ENSP00000509756.1:n.*1663_*1665del | |
| ENST00000689389.1:c.*39_*41del (RAF1) | ENSP00000510213.1:n.*39_*41del | |
| ENST00000689418.1:c.*3881_*3883del (RAF1) | ENSP00000509467.1:n.*3881_*3883del | |
| ENST00000689540.1:n.4354_4356del (RAF1) | ||
| ENST00000689876.1:c.*535_*537del (RAF1) | ENSP00000508535.1:n.*535_*537del | |
| ENST00000689914.1:c.*920_*922del (RAF1) | ENSP00000509847.1:n.*920_*922del | |
| ENST00000690397.1:c.*39_*41del (RAF1) | ENSP00000508730.1:n.*39_*41del | |
| ENST00000690460.1:c.*39_*41del (RAF1) | ENSP00000509106.1:n.*39_*41del | |
| ENST00000690585.1:c.712_714del (RAF1) | ||
| ENST00000690625.1:n.3022_3024del (RAF1) | ||
| ENST00000691396.1:c.*1858_*1860del (RAF1) | ENSP00000510712.1:n.*1858_*1860del | |
| ENST00000691643.1:n.3039_3041del (RAF1) | ||
| ENST00000691724.1:c.*943_*945del (RAF1) | ENSP00000509255.1:n.*943_*945del | |
| ENST00000691779.1:c.*1564_*1566del (RAF1) | ENSP00000508592.1:n.*1564_*1566del | |
| ENST00000691888.1:c.860_862del (RAF1) | ||
| ENST00000691899.1:c.*39_*41del (RAF1) | ENSP00000508763.1:n.*39_*41del | |
| ENST00000692069.1:n.4910_4912del (RAF1) | ||
| ENST00000692093.1:c.*39_*41del (RAF1) | ENSP00000509669.1:n.*39_*41del | |
| ENST00000692311.1:n.2810_2812del (RAF1) | ||
| ENST00000692558.1:n.4569_4571del (RAF1) | ||
| ENST00000692773.1:c.*1723_*1725del (RAF1) | ENSP00000509055.1:n.*1723_*1725del | |
| ENST00000692830.1:c.*1731_*1733del (RAF1) | ENSP00000509461.1:n.*1731_*1733del | |
| ENST00000693312.1:c.*39_*41del (RAF1) | ENSP00000508686.1:n.*39_*41del | |
| ENST00000693664.1:c.*437_*439del (RAF1) | ENSP00000509614.1:n.*437_*439del | |
| ENST00000693705.1:c.*1365_*1367del (RAF1) | ENSP00000510697.1:n.*1365_*1367del | |
| ENST00000251849.9:c.*39_*41del (RAF1) MANE Select | ENSP00000251849.4:n.*39_*41del | |
| ENST00000442415.7:c.*39_*41del (RAF1) | ENSP00000401888.2:n.*39_*41del | |
| ENST00000676541.1:c.*2227_*2229del (MKRN2) | ENSP00000503730.1:n.*2227_*2229del | |
| ENST00000677142.1:c.*2227_*2229del (MKRN2) | ENSP00000504455.1:n.*2227_*2229del | |
| ENST00000677816.1:c.*782_*784del (MKRN2) | ENSP00000502893.1:n.*782_*784del | |
| ENST00000677941.1:n.2290_2292del (MKRN2) | ||
| ENST00000251849.8:c.*39_*41del (RAF1) | ENSP00000251849.4:n.*39_*41del | |
| ENST00000423275.5:c.*1663_*1665del (RAF1) | ENSP00000401088.1:n.*1663_*1665del | |
| ENST00000432427.2:c.1623_1625del (RAF1) | ENSP00000398591.2:n.1623_1625del | |
| ENST00000442415.6:c.*39_*41del (RAF1) | ENSP00000401888.2:n.*39_*41del | |
| ENST00000471449.1:n.675_677del (RAF1) | ||
| NM_002880.3:c.*39_*41del , LRG_413t1:c.*39_*41del (RAF1) | NP_002871.1:n.*39_*41del | |
| XM_005265355.1:c.*39_*41del (RAF1) | XP_005265412.1:n.*39_*41del | |
| XM_005265357.1:c.*39_*41del (RAF1) | XP_005265414.1:n.*39_*41del | |
| XM_005265358.3:c.*39_*41del (RAF1) | XP_005265415.1:n.*39_*41del | |
| XM_005265359.3:c.*39_*41del (RAF1) | XP_005265416.1:n.*39_*41del | |
| XM_011533974.1:c.*39_*41del (RAF1) | XP_011532276.1:n.*39_*41del | |
| XM_011533975.1:c.*39_*41del (RAF1) | XP_011532277.1:n.*39_*41del | |
| NM_001354689.1:c.*39_*41del (RAF1) | NP_001341618.1:n.*39_*41del | |
| NM_001354690.1:c.*39_*41del (RAF1) | NP_001341619.1:n.*39_*41del | |
| NM_001354691.1:c.*39_*41del (RAF1) | NP_001341620.1:n.*39_*41del | |
| NM_001354692.1:c.*39_*41del (RAF1) | NP_001341621.1:n.*39_*41del | |
| NM_001354693.1:c.*39_*41del (RAF1) | NP_001341622.1:n.*39_*41del | |
| NM_001354694.1:c.*39_*41del (RAF1) | NP_001341623.1:n.*39_*41del | |
| NM_001354695.1:c.*39_*41del (RAF1) | NP_001341624.1:n.*39_*41del | |
| NR_148940.1:n.2514_2516del (RAF1) | ||
| NR_148941.1:n.2460_2462del (RAF1) | ||
| NR_148942.1:n.2399_2401del (RAF1) | ||
| XM_011533974.3:c.*39_*41del (RAF1) | XP_011532276.1:n.*39_*41del | |
| XM_017006966.1:c.*39_*41del (RAF1) | XP_016862455.1:n.*39_*41del | |
| NM_001354689.3:c.*39_*41del (RAF1) | NP_001341618.1:n.*39_*41del | |
| NM_001354690.2:c.*39_*41del (RAF1) | NP_001341619.1:n.*39_*41del | |
| NM_001354691.2:c.*39_*41del (RAF1) | NP_001341620.1:n.*39_*41del | |
| NM_001354692.2:c.*39_*41del (RAF1) | NP_001341621.1:n.*39_*41del | |
| NM_001354693.2:c.*39_*41del (RAF1) | NP_001341622.1:n.*39_*41del | |
| NM_001354694.2:c.*39_*41del (RAF1) | NP_001341623.1:n.*39_*41del | |
| NM_001354695.2:c.*39_*41del (RAF1) | NP_001341624.1:n.*39_*41del | |
| NR_148940.2:n.2430_2432del (RAF1) | ||
| NR_148941.2:n.2376_2378del (RAF1) | ||
| NR_148942.2:n.2315_2317del (RAF1) | ||
| NM_001354690.3:c.*39_*41del (RAF1) | NP_001341619.1:n.*39_*41del | |
| NM_001354691.3:c.*39_*41del (RAF1) | NP_001341620.1:n.*39_*41del | |
| NM_001354692.3:c.*39_*41del (RAF1) | NP_001341621.1:n.*39_*41del | |
| NM_001354693.3:c.*39_*41del (RAF1) | NP_001341622.1:n.*39_*41del | |
| NM_001354694.3:c.*39_*41del (RAF1) | NP_001341623.1:n.*39_*41del | |
| NM_001354695.3:c.*39_*41del (RAF1) | NP_001341624.1:n.*39_*41del | |
| NM_002880.4:c.*39_*41del (RAF1) MANE Select | NP_002871.1:n.*39_*41del | |
| NR_148940.3:n.2430_2432del (RAF1) | ||
| NR_148941.3:n.2376_2378del (RAF1) | ||
| NR_148942.3:n.2315_2317del (RAF1) |