Canonical Allele Identifier: CA69616837

Gene: RAF1

Linked Data

• dbSNP Id: rs760136925
• gnomAD v3: 3-12600230-G-A
• gnomAD v4: 3-12600230-G-A
• MyVariant Identifiers: chr3:g.12641729G>A (hg19) ; chr3:g.12600230G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12600230G>A , CM000665.2:g.12600230G>A	GRCh38
NC_000003.11:g.12641729G>A , CM000665.1:g.12641729G>A	GRCh37
NC_000003.10:g.12616729G>A	NCBI36
NG_007467.1:g.68950C>T , LRG_413:g.68950C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*577C>T	ENSP00000401088.1:n.*577C>T
ENST00000432427.3:c.232C>T
ENST00000465826.6:n.503C>T
ENST00000491290.2:n.1289C>T
ENST00000684903.1:c.*589C>T	ENSP00000508612.1:n.*589C>T
ENST00000685348.1:c.*589C>T	ENSP00000510285.1:n.*589C>T
ENST00000685437.1:c.813C>T	ENSP00000508794.1:p.Gly271=
ENST00000685438.1:n.676C>T
ENST00000685653.1:c.912C>T	ENSP00000509968.1:p.Gly304=
ENST00000685738.1:c.912C>T	ENSP00000510156.1:p.Gly304=
ENST00000686409.1:n.1620C>T
ENST00000686455.1:n.1275C>T
ENST00000686479.1:n.1283C>T
ENST00000686762.1:c.912C>T	ENSP00000509767.1:p.Gly304=
ENST00000687257.1:n.1148C>T
ENST00000687326.1:c.912C>T	ENSP00000509665.1:p.Gly304=
ENST00000687486.1:c.182+158C>T
ENST00000687505.1:n.1030C>T
ENST00000687923.1:c.813C>T	ENSP00000510255.1:p.Gly271=
ENST00000687940.1:n.1289C>T
ENST00000688269.1:n.1508C>T
ENST00000688326.1:c.232C>T
ENST00000688444.1:n.1238C>T
ENST00000688543.1:c.813C>T	ENSP00000509612.1:p.Gly271=
ENST00000688625.1:c.*490C>T	ENSP00000509522.1:n.*490C>T
ENST00000688803.1:n.1143C>T
ENST00000689097.1:c.*589C>T	ENSP00000509756.1:n.*589C>T
ENST00000689389.1:c.912C>T	ENSP00000510213.1:p.Gly304=
ENST00000689418.1:c.*589C>T	ENSP00000509467.1:n.*589C>T
ENST00000689481.1:c.*589C>T	ENSP00000510248.1:n.*589C>T
ENST00000689540.1:n.1062C>T
ENST00000689876.1:c.912C>T	ENSP00000508535.1:p.Gly304=
ENST00000689914.1:c.912C>T	ENSP00000509847.1:p.Gly304=
ENST00000690397.1:c.801C>T	ENSP00000508730.1:p.Gly267=
ENST00000690460.1:c.900C>T	ENSP00000509106.1:p.Gly300=
ENST00000690625.1:n.1215C>T
ENST00000691268.1:c.339C>T
ENST00000691396.1:c.*705C>T	ENSP00000510712.1:n.*705C>T
ENST00000691724.1:c.912C>T	ENSP00000509255.1:p.Gly304=
ENST00000691779.1:c.*490C>T	ENSP00000508592.1:n.*490C>T
ENST00000691899.1:c.912C>T	ENSP00000508763.1:p.Gly304=
ENST00000692069.1:n.1135C>T
ENST00000692093.1:c.813C>T	ENSP00000509669.1:p.Gly271=
ENST00000692311.1:n.1393C>T
ENST00000692558.1:n.1277C>T
ENST00000692773.1:c.*649C>T	ENSP00000509055.1:n.*649C>T
ENST00000692830.1:c.*657C>T	ENSP00000509461.1:n.*657C>T
ENST00000693069.1:c.813C>T	ENSP00000510072.1:p.Gly271=
ENST00000693312.1:c.687C>T	ENSP00000508686.1:p.Gly229=
ENST00000693664.1:c.912C>T	ENSP00000509614.1:p.Gly304=
ENST00000693705.1:c.*589C>T	ENSP00000510697.1:n.*589C>T
ENST00000251849.9:c.912C>T MANE Select	ENSP00000251849.4:p.Gly304=
ENST00000442415.7:c.972C>T	ENSP00000401888.2:p.Gly324=
ENST00000251849.8:c.912C>T	ENSP00000251849.4:p.Gly304=
ENST00000423275.5:c.*589C>T	ENSP00000401088.1:n.*589C>T
ENST00000432427.2:c.549C>T	ENSP00000398591.2:p.Gly183=
ENST00000442415.6:c.972C>T	ENSP00000401888.2:p.Gly324=
ENST00000465826.5:n.156C>T
ENST00000491290.1:n.541C>T
NM_002880.3:c.912C>T , LRG_413t1:c.912C>T	NP_002871.1:p.Gly304=
XM_005265355.1:c.912C>T	XP_005265412.1:p.Gly304=
XM_005265357.1:c.813C>T	XP_005265414.1:p.Gly271=
XM_005265358.3:c.669C>T	XP_005265415.1:p.Gly223=
XM_005265359.3:c.570C>T	XP_005265416.1:p.Gly190=
XM_005265360.1:c.912C>T	XP_005265417.1:p.Gly304=
XM_011533974.1:c.912C>T	XP_011532276.1:p.Gly304=
XM_011533975.1:c.669C>T	XP_011532277.1:p.Gly223=
NM_001354689.1:c.972C>T	NP_001341618.1:p.Gly324=
NM_001354690.1:c.912C>T	NP_001341619.1:p.Gly304=
NM_001354691.1:c.669C>T	NP_001341620.1:p.Gly223=
NM_001354692.1:c.669C>T	NP_001341621.1:p.Gly223=
NM_001354693.1:c.813C>T	NP_001341622.1:p.Gly271=
NM_001354694.1:c.729C>T	NP_001341623.1:p.Gly243=
NM_001354695.1:c.570C>T	NP_001341624.1:p.Gly190=
NR_148940.1:n.1327C>T
NR_148941.1:n.1327C>T
NR_148942.1:n.1327C>T
XM_011533974.3:c.912C>T	XP_011532276.1:p.Gly304=
XM_017006966.1:c.813C>T	XP_016862455.1:p.Gly271=
XR_001740227.1:n.1144C>T
NM_001354689.3:c.972C>T	NP_001341618.1:p.Gly324=
NM_001354690.2:c.912C>T	NP_001341619.1:p.Gly304=
NM_001354691.2:c.669C>T	NP_001341620.1:p.Gly223=
NM_001354692.2:c.669C>T	NP_001341621.1:p.Gly223=
NM_001354693.2:c.813C>T	NP_001341622.1:p.Gly271=
NM_001354694.2:c.729C>T	NP_001341623.1:p.Gly243=
NM_001354695.2:c.570C>T	NP_001341624.1:p.Gly190=
NR_148940.2:n.1243C>T
NR_148941.2:n.1243C>T
NR_148942.2:n.1243C>T
NM_001354690.3:c.912C>T	NP_001341619.1:p.Gly304=
NM_001354691.3:c.669C>T	NP_001341620.1:p.Gly223=
NM_001354692.3:c.669C>T	NP_001341621.1:p.Gly223=
NM_001354693.3:c.813C>T	NP_001341622.1:p.Gly271=
NM_001354694.3:c.729C>T	NP_001341623.1:p.Gly243=
NM_001354695.3:c.570C>T	NP_001341624.1:p.Gly190=
NM_002880.4:c.912C>T MANE Select	NP_002871.1:p.Gly304=
NR_148940.3:n.1243C>T
NR_148941.3:n.1243C>T
NR_148942.3:n.1243C>T