Canonical Allele Identifier: CA351509472

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12641757C>A (hg19) ; chr3:g.12600258C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12600258C>A , CM000665.2:g.12600258C>A	GRCh38
NC_000003.11:g.12641757C>A , CM000665.1:g.12641757C>A	GRCh37
NC_000003.10:g.12616757C>A	NCBI36
NG_007467.1:g.68922G>T , LRG_413:g.68922G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*549G>T	ENSP00000401088.1:n.*549G>T
ENST00000432427.3:c.204G>T
ENST00000465826.6:n.475G>T
ENST00000491290.2:n.1261G>T
ENST00000684903.1:c.*561G>T	ENSP00000508612.1:n.*561G>T
ENST00000685348.1:c.*561G>T	ENSP00000510285.1:n.*561G>T
ENST00000685437.1:c.785G>T	ENSP00000508794.1:p.Ser262Ile
ENST00000685438.1:n.648G>T
ENST00000685653.1:c.884G>T	ENSP00000509968.1:p.Ser295Ile
ENST00000685738.1:c.884G>T	ENSP00000510156.1:p.Ser295Ile
ENST00000686409.1:n.1592G>T
ENST00000686455.1:n.1247G>T
ENST00000686479.1:n.1255G>T
ENST00000686762.1:c.884G>T	ENSP00000509767.1:p.Ser295Ile
ENST00000687257.1:n.1120G>T
ENST00000687326.1:c.884G>T	ENSP00000509665.1:p.Ser295Ile
ENST00000687486.1:c.182+130G>T
ENST00000687505.1:n.1002G>T
ENST00000687923.1:c.785G>T	ENSP00000510255.1:p.Ser262Ile
ENST00000687940.1:n.1261G>T
ENST00000688269.1:n.1480G>T
ENST00000688326.1:c.204G>T
ENST00000688444.1:n.1210G>T
ENST00000688543.1:c.785G>T	ENSP00000509612.1:p.Ser262Ile
ENST00000688625.1:c.*462G>T	ENSP00000509522.1:n.*462G>T
ENST00000688803.1:n.1115G>T
ENST00000689097.1:c.*561G>T	ENSP00000509756.1:n.*561G>T
ENST00000689389.1:c.884G>T	ENSP00000510213.1:p.Ser295Ile
ENST00000689418.1:c.*561G>T	ENSP00000509467.1:n.*561G>T
ENST00000689481.1:c.*561G>T	ENSP00000510248.1:n.*561G>T
ENST00000689540.1:n.1034G>T
ENST00000689876.1:c.884G>T	ENSP00000508535.1:p.Ser295Ile
ENST00000689914.1:c.884G>T	ENSP00000509847.1:p.Ser295Ile
ENST00000690397.1:c.773G>T	ENSP00000508730.1:p.Ser258Ile
ENST00000690460.1:c.872G>T	ENSP00000509106.1:p.Ser291Ile
ENST00000690625.1:n.1187G>T
ENST00000691268.1:c.311G>T
ENST00000691396.1:c.*677G>T	ENSP00000510712.1:n.*677G>T
ENST00000691724.1:c.884G>T	ENSP00000509255.1:p.Ser295Ile
ENST00000691779.1:c.*462G>T	ENSP00000508592.1:n.*462G>T
ENST00000691899.1:c.884G>T	ENSP00000508763.1:p.Ser295Ile
ENST00000692069.1:n.1107G>T
ENST00000692093.1:c.785G>T	ENSP00000509669.1:p.Ser262Ile
ENST00000692311.1:n.1365G>T
ENST00000692558.1:n.1249G>T
ENST00000692773.1:c.*621G>T	ENSP00000509055.1:n.*621G>T
ENST00000692830.1:c.*629G>T	ENSP00000509461.1:n.*629G>T
ENST00000693069.1:c.785G>T	ENSP00000510072.1:p.Ser262Ile
ENST00000693312.1:c.659G>T	ENSP00000508686.1:p.Ser220Ile
ENST00000693664.1:c.884G>T	ENSP00000509614.1:p.Ser295Ile
ENST00000693705.1:c.*561G>T	ENSP00000510697.1:n.*561G>T
ENST00000251849.9:c.884G>T MANE Select	ENSP00000251849.4:p.Ser295Ile
ENST00000442415.7:c.944G>T	ENSP00000401888.2:p.Ser315Ile
ENST00000251849.8:c.884G>T	ENSP00000251849.4:p.Ser295Ile
ENST00000423275.5:c.*561G>T	ENSP00000401088.1:n.*561G>T
ENST00000432427.2:c.521G>T	ENSP00000398591.2:p.Ser174Ile
ENST00000442415.6:c.944G>T	ENSP00000401888.2:p.Ser315Ile
ENST00000465826.5:n.128G>T
ENST00000491290.1:n.513G>T
NM_002880.3:c.884G>T , LRG_413t1:c.884G>T	NP_002871.1:p.Ser295Ile
XM_005265355.1:c.884G>T	XP_005265412.1:p.Ser295Ile
XM_005265357.1:c.785G>T	XP_005265414.1:p.Ser262Ile
XM_005265358.3:c.641G>T	XP_005265415.1:p.Ser214Ile
XM_005265359.3:c.542G>T	XP_005265416.1:p.Ser181Ile
XM_005265360.1:c.884G>T	XP_005265417.1:p.Ser295Ile
XM_011533974.1:c.884G>T	XP_011532276.1:p.Ser295Ile
XM_011533975.1:c.641G>T	XP_011532277.1:p.Ser214Ile
NM_001354689.1:c.944G>T	NP_001341618.1:p.Ser315Ile
NM_001354690.1:c.884G>T	NP_001341619.1:p.Ser295Ile
NM_001354691.1:c.641G>T	NP_001341620.1:p.Ser214Ile
NM_001354692.1:c.641G>T	NP_001341621.1:p.Ser214Ile
NM_001354693.1:c.785G>T	NP_001341622.1:p.Ser262Ile
NM_001354694.1:c.701G>T	NP_001341623.1:p.Ser234Ile
NM_001354695.1:c.542G>T	NP_001341624.1:p.Ser181Ile
NR_148940.1:n.1299G>T
NR_148941.1:n.1299G>T
NR_148942.1:n.1299G>T
XM_011533974.3:c.884G>T	XP_011532276.1:p.Ser295Ile
XM_017006966.1:c.785G>T	XP_016862455.1:p.Ser262Ile
XR_001740227.1:n.1116G>T
NM_001354689.3:c.944G>T	NP_001341618.1:p.Ser315Ile
NM_001354690.2:c.884G>T	NP_001341619.1:p.Ser295Ile
NM_001354691.2:c.641G>T	NP_001341620.1:p.Ser214Ile
NM_001354692.2:c.641G>T	NP_001341621.1:p.Ser214Ile
NM_001354693.2:c.785G>T	NP_001341622.1:p.Ser262Ile
NM_001354694.2:c.701G>T	NP_001341623.1:p.Ser234Ile
NM_001354695.2:c.542G>T	NP_001341624.1:p.Ser181Ile
NR_148940.2:n.1215G>T
NR_148941.2:n.1215G>T
NR_148942.2:n.1215G>T
NM_001354690.3:c.884G>T	NP_001341619.1:p.Ser295Ile
NM_001354691.3:c.641G>T	NP_001341620.1:p.Ser214Ile
NM_001354692.3:c.641G>T	NP_001341621.1:p.Ser214Ile
NM_001354693.3:c.785G>T	NP_001341622.1:p.Ser262Ile
NM_001354694.3:c.701G>T	NP_001341623.1:p.Ser234Ile
NM_001354695.3:c.542G>T	NP_001341624.1:p.Ser181Ile
NM_002880.4:c.884G>T MANE Select	NP_002871.1:p.Ser295Ile
NR_148940.3:n.1215G>T
NR_148941.3:n.1215G>T
NR_148942.3:n.1215G>T