Canonical Allele Identifier: CA432274003

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12641756A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12600257A>G , CM000665.2:g.12600257A>G	GRCh38
NC_000003.11:g.12641756A>G , CM000665.1:g.12641756A>G	GRCh37
NC_000003.10:g.12616756A>G	NCBI36
NG_007467.1:g.68923T>C , LRG_413:g.68923T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*550T>C	ENSP00000401088.1:n.*550T>C
ENST00000432427.3:c.205T>C
ENST00000465826.6:n.476T>C
ENST00000491290.2:n.1262T>C
ENST00000684903.1:c.*562T>C	ENSP00000508612.1:n.*562T>C
ENST00000685348.1:c.*562T>C	ENSP00000510285.1:n.*562T>C
ENST00000685437.1:c.786T>C	ENSP00000508794.1:p.Ser262=
ENST00000685438.1:n.649T>C
ENST00000685653.1:c.885T>C	ENSP00000509968.1:p.Ser295=
ENST00000685738.1:c.885T>C	ENSP00000510156.1:p.Ser295=
ENST00000686409.1:n.1593T>C
ENST00000686455.1:n.1248T>C
ENST00000686479.1:n.1256T>C
ENST00000686762.1:c.885T>C	ENSP00000509767.1:p.Ser295=
ENST00000687257.1:n.1121T>C
ENST00000687326.1:c.885T>C	ENSP00000509665.1:p.Ser295=
ENST00000687486.1:c.182+131T>C
ENST00000687505.1:n.1003T>C
ENST00000687923.1:c.786T>C	ENSP00000510255.1:p.Ser262=
ENST00000687940.1:n.1262T>C
ENST00000688269.1:n.1481T>C
ENST00000688326.1:c.205T>C
ENST00000688444.1:n.1211T>C
ENST00000688543.1:c.786T>C	ENSP00000509612.1:p.Ser262=
ENST00000688625.1:c.*463T>C	ENSP00000509522.1:n.*463T>C
ENST00000688803.1:n.1116T>C
ENST00000689097.1:c.*562T>C	ENSP00000509756.1:n.*562T>C
ENST00000689389.1:c.885T>C	ENSP00000510213.1:p.Ser295=
ENST00000689418.1:c.*562T>C	ENSP00000509467.1:n.*562T>C
ENST00000689481.1:c.*562T>C	ENSP00000510248.1:n.*562T>C
ENST00000689540.1:n.1035T>C
ENST00000689876.1:c.885T>C	ENSP00000508535.1:p.Ser295=
ENST00000689914.1:c.885T>C	ENSP00000509847.1:p.Ser295=
ENST00000690397.1:c.774T>C	ENSP00000508730.1:p.Ser258=
ENST00000690460.1:c.873T>C	ENSP00000509106.1:p.Ser291=
ENST00000690625.1:n.1188T>C
ENST00000691268.1:c.312T>C
ENST00000691396.1:c.*678T>C	ENSP00000510712.1:n.*678T>C
ENST00000691724.1:c.885T>C	ENSP00000509255.1:p.Ser295=
ENST00000691779.1:c.*463T>C	ENSP00000508592.1:n.*463T>C
ENST00000691899.1:c.885T>C	ENSP00000508763.1:p.Ser295=
ENST00000692069.1:n.1108T>C
ENST00000692093.1:c.786T>C	ENSP00000509669.1:p.Ser262=
ENST00000692311.1:n.1366T>C
ENST00000692558.1:n.1250T>C
ENST00000692773.1:c.*622T>C	ENSP00000509055.1:n.*622T>C
ENST00000692830.1:c.*630T>C	ENSP00000509461.1:n.*630T>C
ENST00000693069.1:c.786T>C	ENSP00000510072.1:p.Ser262=
ENST00000693312.1:c.660T>C	ENSP00000508686.1:p.Ser220=
ENST00000693664.1:c.885T>C	ENSP00000509614.1:p.Ser295=
ENST00000693705.1:c.*562T>C	ENSP00000510697.1:n.*562T>C
ENST00000251849.9:c.885T>C MANE Select	ENSP00000251849.4:p.Ser295=
ENST00000442415.7:c.945T>C	ENSP00000401888.2:p.Ser315=
ENST00000251849.8:c.885T>C	ENSP00000251849.4:p.Ser295=
ENST00000423275.5:c.*562T>C	ENSP00000401088.1:n.*562T>C
ENST00000432427.2:c.522T>C	ENSP00000398591.2:p.Ser174=
ENST00000442415.6:c.945T>C	ENSP00000401888.2:p.Ser315=
ENST00000465826.5:n.129T>C
ENST00000491290.1:n.514T>C
NM_002880.3:c.885T>C , LRG_413t1:c.885T>C	NP_002871.1:p.Ser295=
XM_005265355.1:c.885T>C	XP_005265412.1:p.Ser295=
XM_005265357.1:c.786T>C	XP_005265414.1:p.Ser262=
XM_005265358.3:c.642T>C	XP_005265415.1:p.Ser214=
XM_005265359.3:c.543T>C	XP_005265416.1:p.Ser181=
XM_005265360.1:c.885T>C	XP_005265417.1:p.Ser295=
XM_011533974.1:c.885T>C	XP_011532276.1:p.Ser295=
XM_011533975.1:c.642T>C	XP_011532277.1:p.Ser214=
NM_001354689.1:c.945T>C	NP_001341618.1:p.Ser315=
NM_001354690.1:c.885T>C	NP_001341619.1:p.Ser295=
NM_001354691.1:c.642T>C	NP_001341620.1:p.Ser214=
NM_001354692.1:c.642T>C	NP_001341621.1:p.Ser214=
NM_001354693.1:c.786T>C	NP_001341622.1:p.Ser262=
NM_001354694.1:c.702T>C	NP_001341623.1:p.Ser234=
NM_001354695.1:c.543T>C	NP_001341624.1:p.Ser181=
NR_148940.1:n.1300T>C
NR_148941.1:n.1300T>C
NR_148942.1:n.1300T>C
XM_011533974.3:c.885T>C	XP_011532276.1:p.Ser295=
XM_017006966.1:c.786T>C	XP_016862455.1:p.Ser262=
XR_001740227.1:n.1117T>C
NM_001354689.3:c.945T>C	NP_001341618.1:p.Ser315=
NM_001354690.2:c.885T>C	NP_001341619.1:p.Ser295=
NM_001354691.2:c.642T>C	NP_001341620.1:p.Ser214=
NM_001354692.2:c.642T>C	NP_001341621.1:p.Ser214=
NM_001354693.2:c.786T>C	NP_001341622.1:p.Ser262=
NM_001354694.2:c.702T>C	NP_001341623.1:p.Ser234=
NM_001354695.2:c.543T>C	NP_001341624.1:p.Ser181=
NR_148940.2:n.1216T>C
NR_148941.2:n.1216T>C
NR_148942.2:n.1216T>C
NM_001354690.3:c.885T>C	NP_001341619.1:p.Ser295=
NM_001354691.3:c.642T>C	NP_001341620.1:p.Ser214=
NM_001354692.3:c.642T>C	NP_001341621.1:p.Ser214=
NM_001354693.3:c.786T>C	NP_001341622.1:p.Ser262=
NM_001354694.3:c.702T>C	NP_001341623.1:p.Ser234=
NM_001354695.3:c.543T>C	NP_001341624.1:p.Ser181=
NM_002880.4:c.885T>C MANE Select	NP_002871.1:p.Ser295=
NR_148940.3:n.1216T>C
NR_148941.3:n.1216T>C
NR_148942.3:n.1216T>C