Canonical Allele Identifier: CA432273151
Gene: RAF1 HGNC NCBI

Linked Data

gnomAD v4: 3-12590905-G-A
MyVariant Identifiers: chr3:g.12632404G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590905G>A , CM000665.2:g.12590905G>A GRCh38
NC_000003.11:g.12632404G>A , CM000665.1:g.12632404G>A GRCh37
NC_000003.10:g.12607404G>A NCBI36
NG_007467.1:g.78275C>T , LRG_413:g.78275C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*928C>T ENSP00000401088.1:n.*928C>T
ENST00000432427.3:c.580C>T
ENST00000460610.2:n.57C>T
ENST00000465826.6:n.854C>T
ENST00000475353.2:n.1185C>T
ENST00000494557.2:n.1074C>T
ENST00000684903.1:c.*940C>T ENSP00000508612.1:n.*940C>T
ENST00000685348.1:c.*940C>T ENSP00000510285.1:n.*940C>T
ENST00000685437.1:c.1164C>T ENSP00000508794.1:p.Thr388=
ENST00000685653.1:c.1263C>T ENSP00000509968.1:p.Thr421=
ENST00000685738.1:c.*227C>T ENSP00000510156.1:n.*227C>T
ENST00000686409.1:n.2314C>T
ENST00000686455.1:n.1626C>T
ENST00000686762.1:c.1263C>T ENSP00000509767.1:p.Thr421=
ENST00000687257.1:n.1499C>T
ENST00000687326.1:c.*197C>T ENSP00000509665.1:n.*197C>T
ENST00000687505.1:n.1381C>T
ENST00000687923.1:c.1152C>T ENSP00000510255.1:p.Thr384=
ENST00000687940.1:n.1640C>T
ENST00000688269.1:n.1859C>T
ENST00000688326.1:c.696C>T
ENST00000688444.1:n.1589C>T
ENST00000688543.1:c.1164C>T ENSP00000509612.1:p.Thr388=
ENST00000688625.1:c.*841C>T ENSP00000509522.1:n.*841C>T
ENST00000688803.1:n.1494C>T
ENST00000688914.1:n.249C>T
ENST00000689097.1:c.*940C>T ENSP00000509756.1:n.*940C>T
ENST00000689389.1:c.1193+803C>T ENSP00000510213.1:n.1193+803C>T
ENST00000689418.1:c.*940C>T ENSP00000509467.1:n.*940C>T
ENST00000689481.1:c.*940C>T ENSP00000510248.1:n.*940C>T
ENST00000689540.1:n.1413C>T
ENST00000689876.1:c.1263C>T ENSP00000508535.1:p.Thr421=
ENST00000689914.1:c.*197C>T ENSP00000509847.1:n.*197C>T
ENST00000690397.1:c.1152C>T ENSP00000508730.1:p.Thr384=
ENST00000690460.1:c.1251C>T ENSP00000509106.1:p.Thr417=
ENST00000690585.1:c.155C>T
ENST00000690625.1:n.2299C>T
ENST00000691396.1:c.*1115C>T ENSP00000510712.1:n.*1115C>T
ENST00000691724.1:c.*220C>T ENSP00000509255.1:n.*220C>T
ENST00000691779.1:c.*841C>T ENSP00000508592.1:n.*841C>T
ENST00000691888.1:c.155C>T
ENST00000691899.1:c.1263C>T ENSP00000508763.1:p.Thr421=
ENST00000692069.1:n.1829C>T
ENST00000692093.1:c.1164C>T ENSP00000509669.1:p.Thr388=
ENST00000692311.1:n.2087C>T
ENST00000692558.1:n.1628C>T
ENST00000692773.1:c.*1000C>T ENSP00000509055.1:n.*1000C>T
ENST00000692830.1:c.*1008C>T ENSP00000509461.1:n.*1008C>T
ENST00000693069.1:c.*197C>T ENSP00000510072.1:n.*197C>T
ENST00000693312.1:c.1038C>T ENSP00000508686.1:p.Thr346=
ENST00000693664.1:c.1263C>T ENSP00000509614.1:p.Thr421=
ENST00000693705.1:c.*940C>T ENSP00000510697.1:n.*940C>T
ENST00000251849.9:c.1263C>T MANE Select ENSP00000251849.4:p.Thr421=
ENST00000442415.7:c.1323C>T ENSP00000401888.2:p.Thr441=
ENST00000251849.8:c.1263C>T ENSP00000251849.4:p.Thr421=
ENST00000423275.5:c.*940C>T ENSP00000401088.1:n.*940C>T
ENST00000432427.2:c.900C>T ENSP00000398591.2:p.Thr300=
ENST00000442415.6:c.1323C>T ENSP00000401888.2:p.Thr441=
ENST00000460610.1:n.220C>T
ENST00000465826.5:n.620C>T
ENST00000475353.1:n.431C>T
ENST00000494557.1:n.279C>T
NM_002880.3:c.1263C>T , LRG_413t1:c.1263C>T NP_002871.1:p.Thr421=
XM_005265355.1:c.1263C>T XP_005265412.1:p.Thr421=
XM_005265357.1:c.1164C>T XP_005265414.1:p.Thr388=
XM_005265358.3:c.1020C>T XP_005265415.1:p.Thr340=
XM_005265359.3:c.921C>T XP_005265416.1:p.Thr307=
XM_005265360.1:c.1263C>T XP_005265417.1:p.Thr421=
XM_011533974.1:c.1263C>T XP_011532276.1:p.Thr421=
XM_011533975.1:c.1020C>T XP_011532277.1:p.Thr340=
NM_001354689.1:c.1323C>T NP_001341618.1:p.Thr441=
NM_001354690.1:c.1263C>T NP_001341619.1:p.Thr421=
NM_001354691.1:c.1020C>T NP_001341620.1:p.Thr340=
NM_001354692.1:c.1020C>T NP_001341621.1:p.Thr340=
NM_001354693.1:c.1164C>T NP_001341622.1:p.Thr388=
NM_001354694.1:c.1080C>T NP_001341623.1:p.Thr360=
NM_001354695.1:c.921C>T NP_001341624.1:p.Thr307=
NR_148940.1:n.1791C>T
NR_148941.1:n.1737C>T
NR_148942.1:n.1676C>T
XM_011533974.3:c.1263C>T XP_011532276.1:p.Thr421=
XM_017006966.1:c.1164C>T XP_016862455.1:p.Thr388=
NM_001354689.3:c.1323C>T NP_001341618.1:p.Thr441=
NM_001354690.2:c.1263C>T NP_001341619.1:p.Thr421=
NM_001354691.2:c.1020C>T NP_001341620.1:p.Thr340=
NM_001354692.2:c.1020C>T NP_001341621.1:p.Thr340=
NM_001354693.2:c.1164C>T NP_001341622.1:p.Thr388=
NM_001354694.2:c.1080C>T NP_001341623.1:p.Thr360=
NM_001354695.2:c.921C>T NP_001341624.1:p.Thr307=
NR_148940.2:n.1707C>T
NR_148941.2:n.1653C>T
NR_148942.2:n.1592C>T
NM_001354690.3:c.1263C>T NP_001341619.1:p.Thr421=
NM_001354691.3:c.1020C>T NP_001341620.1:p.Thr340=
NM_001354692.3:c.1020C>T NP_001341621.1:p.Thr340=
NM_001354693.3:c.1164C>T NP_001341622.1:p.Thr388=
NM_001354694.3:c.1080C>T NP_001341623.1:p.Thr360=
NM_001354695.3:c.921C>T NP_001341624.1:p.Thr307=
NM_002880.4:c.1263C>T MANE Select NP_002871.1:p.Thr421=
NR_148940.3:n.1707C>T
NR_148941.3:n.1653C>T
NR_148942.3:n.1592C>T