Canonical Allele Identifier: CA432273749

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12641221A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12599722A>C , CM000665.2:g.12599722A>C	GRCh38
NC_000003.11:g.12641221A>C , CM000665.1:g.12641221A>C	GRCh37
NC_000003.10:g.12616221A>C	NCBI36
NG_007467.1:g.69458T>G , LRG_413:g.69458T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*742T>G	ENSP00000401088.1:n.*742T>G
ENST00000432427.3:c.397T>G
ENST00000465826.6:n.668T>G
ENST00000491290.2:n.1454T>G
ENST00000684903.1:c.*754T>G	ENSP00000508612.1:n.*754T>G
ENST00000685348.1:c.*754T>G	ENSP00000510285.1:n.*754T>G
ENST00000685437.1:c.978T>G	ENSP00000508794.1:p.Ser326=
ENST00000685653.1:c.1077T>G	ENSP00000509968.1:p.Ser359=
ENST00000685738.1:c.1077T>G	ENSP00000510156.1:p.Ser359=
ENST00000686409.1:n.2128T>G
ENST00000686455.1:n.1440T>G
ENST00000686479.1:n.1448T>G
ENST00000686762.1:c.1077T>G	ENSP00000509767.1:p.Ser359=
ENST00000687257.1:n.1313T>G
ENST00000687326.1:c.1077T>G	ENSP00000509665.1:p.Ser359=
ENST00000687486.1:c.269T>G
ENST00000687505.1:n.1195T>G
ENST00000687923.1:c.978T>G	ENSP00000510255.1:p.Ser326=
ENST00000687940.1:n.1454T>G
ENST00000688269.1:n.1673T>G
ENST00000688326.1:c.397T>G
ENST00000688444.1:n.1403T>G
ENST00000688543.1:c.978T>G	ENSP00000509612.1:p.Ser326=
ENST00000688625.1:c.*655T>G	ENSP00000509522.1:n.*655T>G
ENST00000688803.1:n.1308T>G
ENST00000688914.1:n.63T>G
ENST00000689097.1:c.*754T>G	ENSP00000509756.1:n.*754T>G
ENST00000689389.1:c.1077T>G	ENSP00000510213.1:p.Ser359=
ENST00000689418.1:c.*754T>G	ENSP00000509467.1:n.*754T>G
ENST00000689481.1:c.*754T>G	ENSP00000510248.1:n.*754T>G
ENST00000689540.1:n.1227T>G
ENST00000689876.1:c.1077T>G	ENSP00000508535.1:p.Ser359=
ENST00000689914.1:c.1077T>G	ENSP00000509847.1:p.Ser359=
ENST00000690397.1:c.966T>G	ENSP00000508730.1:p.Ser322=
ENST00000690460.1:c.1065T>G	ENSP00000509106.1:p.Ser355=
ENST00000690625.1:n.1380T>G
ENST00000691268.1:c.504T>G
ENST00000691396.1:c.*870T>G	ENSP00000510712.1:n.*870T>G
ENST00000691724.1:c.*34T>G	ENSP00000509255.1:n.*34T>G
ENST00000691779.1:c.*655T>G	ENSP00000508592.1:n.*655T>G
ENST00000691899.1:c.1077T>G	ENSP00000508763.1:p.Ser359=
ENST00000692069.1:n.1643T>G
ENST00000692093.1:c.978T>G	ENSP00000509669.1:p.Ser326=
ENST00000692311.1:n.1901T>G
ENST00000692558.1:n.1442T>G
ENST00000692773.1:c.*814T>G	ENSP00000509055.1:n.*814T>G
ENST00000692830.1:c.*822T>G	ENSP00000509461.1:n.*822T>G
ENST00000693069.1:c.978T>G	ENSP00000510072.1:p.Ser326=
ENST00000693312.1:c.852T>G	ENSP00000508686.1:p.Ser284=
ENST00000693664.1:c.1077T>G	ENSP00000509614.1:p.Ser359=
ENST00000693705.1:c.*754T>G	ENSP00000510697.1:n.*754T>G
ENST00000251849.9:c.1077T>G MANE Select	ENSP00000251849.4:p.Ser359=
ENST00000442415.7:c.1137T>G	ENSP00000401888.2:p.Ser379=
ENST00000251849.8:c.1077T>G	ENSP00000251849.4:p.Ser359=
ENST00000423275.5:c.*754T>G	ENSP00000401088.1:n.*754T>G
ENST00000432427.2:c.714T>G	ENSP00000398591.2:p.Ser238=
ENST00000442415.6:c.1137T>G	ENSP00000401888.2:p.Ser379=
ENST00000460610.1:n.34T>G
ENST00000465826.5:n.321T>G
NM_002880.3:c.1077T>G , LRG_413t1:c.1077T>G	NP_002871.1:p.Ser359=
XM_005265355.1:c.1077T>G	XP_005265412.1:p.Ser359=
XM_005265357.1:c.978T>G	XP_005265414.1:p.Ser326=
XM_005265358.3:c.834T>G	XP_005265415.1:p.Ser278=
XM_005265359.3:c.735T>G	XP_005265416.1:p.Ser245=
XM_005265360.1:c.1077T>G	XP_005265417.1:p.Ser359=
XM_011533974.1:c.1077T>G	XP_011532276.1:p.Ser359=
XM_011533975.1:c.834T>G	XP_011532277.1:p.Ser278=
NM_001354689.1:c.1137T>G	NP_001341618.1:p.Ser379=
NM_001354690.1:c.1077T>G	NP_001341619.1:p.Ser359=
NM_001354691.1:c.834T>G	NP_001341620.1:p.Ser278=
NM_001354692.1:c.834T>G	NP_001341621.1:p.Ser278=
NM_001354693.1:c.978T>G	NP_001341622.1:p.Ser326=
NM_001354694.1:c.894T>G	NP_001341623.1:p.Ser298=
NM_001354695.1:c.735T>G	NP_001341624.1:p.Ser245=
NR_148940.1:n.1492T>G
NR_148941.1:n.1492T>G
NR_148942.1:n.1490T>G
XM_011533974.3:c.1077T>G	XP_011532276.1:p.Ser359=
XM_017006966.1:c.978T>G	XP_016862455.1:p.Ser326=
XR_001740227.1:n.1309T>G
NM_001354689.3:c.1137T>G	NP_001341618.1:p.Ser379=
NM_001354690.2:c.1077T>G	NP_001341619.1:p.Ser359=
NM_001354691.2:c.834T>G	NP_001341620.1:p.Ser278=
NM_001354692.2:c.834T>G	NP_001341621.1:p.Ser278=
NM_001354693.2:c.978T>G	NP_001341622.1:p.Ser326=
NM_001354694.2:c.894T>G	NP_001341623.1:p.Ser298=
NM_001354695.2:c.735T>G	NP_001341624.1:p.Ser245=
NR_148940.2:n.1408T>G
NR_148941.2:n.1408T>G
NR_148942.2:n.1406T>G
NM_001354690.3:c.1077T>G	NP_001341619.1:p.Ser359=
NM_001354691.3:c.834T>G	NP_001341620.1:p.Ser278=
NM_001354692.3:c.834T>G	NP_001341621.1:p.Ser278=
NM_001354693.3:c.978T>G	NP_001341622.1:p.Ser326=
NM_001354694.3:c.894T>G	NP_001341623.1:p.Ser298=
NM_001354695.3:c.735T>G	NP_001341624.1:p.Ser245=
NM_002880.4:c.1077T>G MANE Select	NP_002871.1:p.Ser359=
NR_148940.3:n.1408T>G
NR_148941.3:n.1408T>G
NR_148942.3:n.1406T>G