Canonical Allele Identifier: CA432274283
Gene: RAF1 HGNC NCBI

Linked Data

dbSNP Id: rs2125397271
MyVariant Identifiers: chr3:g.12645665G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12604166G>A , CM000665.2:g.12604166G>A GRCh38
NC_000003.11:g.12645665G>A , CM000665.1:g.12645665G>A GRCh37
NC_000003.10:g.12620665G>A NCBI36
NG_007467.1:g.65014C>T , LRG_413:g.65014C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000416093.2:c.*481C>T ENSP00000391265.2:n.*481C>T
ENST00000423275.6:c.*481C>T ENSP00000401088.1:n.*481C>T
ENST00000432427.3:c.124C>T
ENST00000465826.6:n.395C>T
ENST00000491290.2:n.1181C>T
ENST00000684903.1:c.*481C>T ENSP00000508612.1:n.*481C>T
ENST00000685348.1:c.*481C>T ENSP00000510285.1:n.*481C>T
ENST00000685437.1:c.705C>T ENSP00000508794.1:p.Thr235=
ENST00000685653.1:c.804C>T ENSP00000509968.1:p.Thr268=
ENST00000685738.1:c.804C>T ENSP00000510156.1:p.Thr268=
ENST00000685959.1:c.804C>T ENSP00000510452.1:p.Thr268=
ENST00000686409.1:n.1404C>T
ENST00000686455.1:n.1167C>T
ENST00000686479.1:n.1175C>T
ENST00000686762.1:c.804C>T ENSP00000509767.1:p.Thr268=
ENST00000687257.1:n.1040C>T
ENST00000687326.1:c.804C>T ENSP00000509665.1:p.Thr268=
ENST00000687486.1:c.124C>T
ENST00000687505.1:n.922C>T
ENST00000687923.1:c.705C>T ENSP00000510255.1:p.Thr235=
ENST00000687940.1:n.1181C>T
ENST00000688269.1:n.1412C>T
ENST00000688326.1:c.124C>T
ENST00000688444.1:n.1130C>T
ENST00000688543.1:c.705C>T ENSP00000509612.1:p.Thr235=
ENST00000688625.1:c.*382C>T ENSP00000509522.1:n.*382C>T
ENST00000688803.1:n.1035C>T
ENST00000689033.1:c.804C>T ENSP00000508983.1:p.Thr268=
ENST00000689097.1:c.*481C>T ENSP00000509756.1:n.*481C>T
ENST00000689389.1:c.804C>T ENSP00000510213.1:p.Thr268=
ENST00000689418.1:c.*481C>T ENSP00000509467.1:n.*481C>T
ENST00000689481.1:c.*481C>T ENSP00000510248.1:n.*481C>T
ENST00000689540.1:n.954C>T
ENST00000689876.1:c.804C>T ENSP00000508535.1:p.Thr268=
ENST00000689914.1:c.804C>T ENSP00000509847.1:p.Thr268=
ENST00000690397.1:c.705C>T ENSP00000508730.1:p.Thr235=
ENST00000690460.1:c.804C>T ENSP00000509106.1:p.Thr268=
ENST00000690625.1:n.1107C>T
ENST00000691268.1:c.262-3751C>T
ENST00000691396.1:c.*597C>T ENSP00000510712.1:n.*597C>T
ENST00000691724.1:c.804C>T ENSP00000509255.1:p.Thr268=
ENST00000691779.1:c.*382C>T ENSP00000508592.1:n.*382C>T
ENST00000691899.1:c.804C>T ENSP00000508763.1:p.Thr268=
ENST00000692093.1:c.705C>T ENSP00000509669.1:p.Thr235=
ENST00000692311.1:n.1177C>T
ENST00000692558.1:n.1169C>T
ENST00000692773.1:c.*481C>T ENSP00000509055.1:n.*481C>T
ENST00000692830.1:c.*549C>T ENSP00000509461.1:n.*549C>T
ENST00000693069.1:c.705C>T ENSP00000510072.1:p.Thr235=
ENST00000693312.1:c.579C>T ENSP00000508686.1:p.Thr193=
ENST00000693664.1:c.804C>T ENSP00000509614.1:p.Thr268=
ENST00000693705.1:c.*481C>T ENSP00000510697.1:n.*481C>T
ENST00000251849.9:c.804C>T MANE Select ENSP00000251849.4:p.Thr268=
ENST00000442415.7:c.804C>T ENSP00000401888.2:p.Thr268=
ENST00000251849.8:c.804C>T ENSP00000251849.4:p.Thr268=
ENST00000416093.1:c.*382C>T ENSP00000391265.1:n.*382C>T
ENST00000423275.5:c.*481C>T ENSP00000401088.1:n.*481C>T
ENST00000432427.2:c.441C>T ENSP00000398591.2:p.Thr147=
ENST00000442415.6:c.804C>T ENSP00000401888.2:p.Thr268=
ENST00000465826.5:n.48C>T
ENST00000491290.1:n.325C>T
NM_002880.3:c.804C>T , LRG_413t1:c.804C>T NP_002871.1:p.Thr268=
XM_005265355.1:c.804C>T XP_005265412.1:p.Thr268=
XM_005265357.1:c.705C>T XP_005265414.1:p.Thr235=
XM_005265358.3:c.561C>T XP_005265415.1:p.Thr187=
XM_005265359.3:c.462C>T XP_005265416.1:p.Thr154=
XM_005265360.1:c.804C>T XP_005265417.1:p.Thr268=
XM_011533974.1:c.804C>T XP_011532276.1:p.Thr268=
XM_011533975.1:c.561C>T XP_011532277.1:p.Thr187=
NM_001354689.1:c.804C>T NP_001341618.1:p.Thr268=
NM_001354690.1:c.804C>T NP_001341619.1:p.Thr268=
NM_001354691.1:c.561C>T NP_001341620.1:p.Thr187=
NM_001354692.1:c.561C>T NP_001341621.1:p.Thr187=
NM_001354693.1:c.705C>T NP_001341622.1:p.Thr235=
NM_001354694.1:c.561C>T NP_001341623.1:p.Thr187=
NM_001354695.1:c.462C>T NP_001341624.1:p.Thr154=
NR_148940.1:n.1219C>T
NR_148941.1:n.1219C>T
NR_148942.1:n.1219C>T
XM_011533974.3:c.804C>T XP_011532276.1:p.Thr268=
XM_017006966.1:c.705C>T XP_016862455.1:p.Thr235=
XR_001740227.1:n.1036C>T
NM_001354689.3:c.804C>T NP_001341618.1:p.Thr268=
NM_001354690.2:c.804C>T NP_001341619.1:p.Thr268=
NM_001354691.2:c.561C>T NP_001341620.1:p.Thr187=
NM_001354692.2:c.561C>T NP_001341621.1:p.Thr187=
NM_001354693.2:c.705C>T NP_001341622.1:p.Thr235=
NM_001354694.2:c.561C>T NP_001341623.1:p.Thr187=
NM_001354695.2:c.462C>T NP_001341624.1:p.Thr154=
NR_148940.2:n.1135C>T
NR_148941.2:n.1135C>T
NR_148942.2:n.1135C>T
NM_001354690.3:c.804C>T NP_001341619.1:p.Thr268=
NM_001354691.3:c.561C>T NP_001341620.1:p.Thr187=
NM_001354692.3:c.561C>T NP_001341621.1:p.Thr187=
NM_001354693.3:c.705C>T NP_001341622.1:p.Thr235=
NM_001354694.3:c.561C>T NP_001341623.1:p.Thr187=
NM_001354695.3:c.462C>T NP_001341624.1:p.Thr154=
NM_002880.4:c.804C>T MANE Select NP_002871.1:p.Thr268=
NR_148940.3:n.1135C>T
NR_148941.3:n.1135C>T
NR_148942.3:n.1135C>T