Canonical Allele Identifier: CA432273983

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12641741C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12600242C>A , CM000665.2:g.12600242C>A	GRCh38
NC_000003.11:g.12641741C>A , CM000665.1:g.12641741C>A	GRCh37
NC_000003.10:g.12616741C>A	NCBI36
NG_007467.1:g.68938G>T , LRG_413:g.68938G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*565G>T	ENSP00000401088.1:n.*565G>T
ENST00000432427.3:c.220G>T
ENST00000465826.6:n.491G>T
ENST00000491290.2:n.1277G>T
ENST00000684903.1:c.*577G>T	ENSP00000508612.1:n.*577G>T
ENST00000685348.1:c.*577G>T	ENSP00000510285.1:n.*577G>T
ENST00000685437.1:c.801G>T	ENSP00000508794.1:p.Leu267=
ENST00000685438.1:n.664G>T
ENST00000685653.1:c.900G>T	ENSP00000509968.1:p.Leu300=
ENST00000685738.1:c.900G>T	ENSP00000510156.1:p.Leu300=
ENST00000686409.1:n.1608G>T
ENST00000686455.1:n.1263G>T
ENST00000686479.1:n.1271G>T
ENST00000686762.1:c.900G>T	ENSP00000509767.1:p.Leu300=
ENST00000687257.1:n.1136G>T
ENST00000687326.1:c.900G>T	ENSP00000509665.1:p.Leu300=
ENST00000687486.1:c.182+146G>T
ENST00000687505.1:n.1018G>T
ENST00000687923.1:c.801G>T	ENSP00000510255.1:p.Leu267=
ENST00000687940.1:n.1277G>T
ENST00000688269.1:n.1496G>T
ENST00000688326.1:c.220G>T
ENST00000688444.1:n.1226G>T
ENST00000688543.1:c.801G>T	ENSP00000509612.1:p.Leu267=
ENST00000688625.1:c.*478G>T	ENSP00000509522.1:n.*478G>T
ENST00000688803.1:n.1131G>T
ENST00000689097.1:c.*577G>T	ENSP00000509756.1:n.*577G>T
ENST00000689389.1:c.900G>T	ENSP00000510213.1:p.Leu300=
ENST00000689418.1:c.*577G>T	ENSP00000509467.1:n.*577G>T
ENST00000689481.1:c.*577G>T	ENSP00000510248.1:n.*577G>T
ENST00000689540.1:n.1050G>T
ENST00000689876.1:c.900G>T	ENSP00000508535.1:p.Leu300=
ENST00000689914.1:c.900G>T	ENSP00000509847.1:p.Leu300=
ENST00000690397.1:c.789G>T	ENSP00000508730.1:p.Leu263=
ENST00000690460.1:c.888G>T	ENSP00000509106.1:p.Leu296=
ENST00000690625.1:n.1203G>T
ENST00000691268.1:c.327G>T
ENST00000691396.1:c.*693G>T	ENSP00000510712.1:n.*693G>T
ENST00000691724.1:c.900G>T	ENSP00000509255.1:p.Leu300=
ENST00000691779.1:c.*478G>T	ENSP00000508592.1:n.*478G>T
ENST00000691899.1:c.900G>T	ENSP00000508763.1:p.Leu300=
ENST00000692069.1:n.1123G>T
ENST00000692093.1:c.801G>T	ENSP00000509669.1:p.Leu267=
ENST00000692311.1:n.1381G>T
ENST00000692558.1:n.1265G>T
ENST00000692773.1:c.*637G>T	ENSP00000509055.1:n.*637G>T
ENST00000692830.1:c.*645G>T	ENSP00000509461.1:n.*645G>T
ENST00000693069.1:c.801G>T	ENSP00000510072.1:p.Leu267=
ENST00000693312.1:c.675G>T	ENSP00000508686.1:p.Leu225=
ENST00000693664.1:c.900G>T	ENSP00000509614.1:p.Leu300=
ENST00000693705.1:c.*577G>T	ENSP00000510697.1:n.*577G>T
ENST00000251849.9:c.900G>T MANE Select	ENSP00000251849.4:p.Leu300=
ENST00000442415.7:c.960G>T	ENSP00000401888.2:p.Leu320=
ENST00000251849.8:c.900G>T	ENSP00000251849.4:p.Leu300=
ENST00000423275.5:c.*577G>T	ENSP00000401088.1:n.*577G>T
ENST00000432427.2:c.537G>T	ENSP00000398591.2:p.Leu179=
ENST00000442415.6:c.960G>T	ENSP00000401888.2:p.Leu320=
ENST00000465826.5:n.144G>T
ENST00000491290.1:n.529G>T
NM_002880.3:c.900G>T , LRG_413t1:c.900G>T	NP_002871.1:p.Leu300=
XM_005265355.1:c.900G>T	XP_005265412.1:p.Leu300=
XM_005265357.1:c.801G>T	XP_005265414.1:p.Leu267=
XM_005265358.3:c.657G>T	XP_005265415.1:p.Leu219=
XM_005265359.3:c.558G>T	XP_005265416.1:p.Leu186=
XM_005265360.1:c.900G>T	XP_005265417.1:p.Leu300=
XM_011533974.1:c.900G>T	XP_011532276.1:p.Leu300=
XM_011533975.1:c.657G>T	XP_011532277.1:p.Leu219=
NM_001354689.1:c.960G>T	NP_001341618.1:p.Leu320=
NM_001354690.1:c.900G>T	NP_001341619.1:p.Leu300=
NM_001354691.1:c.657G>T	NP_001341620.1:p.Leu219=
NM_001354692.1:c.657G>T	NP_001341621.1:p.Leu219=
NM_001354693.1:c.801G>T	NP_001341622.1:p.Leu267=
NM_001354694.1:c.717G>T	NP_001341623.1:p.Leu239=
NM_001354695.1:c.558G>T	NP_001341624.1:p.Leu186=
NR_148940.1:n.1315G>T
NR_148941.1:n.1315G>T
NR_148942.1:n.1315G>T
XM_011533974.3:c.900G>T	XP_011532276.1:p.Leu300=
XM_017006966.1:c.801G>T	XP_016862455.1:p.Leu267=
XR_001740227.1:n.1132G>T
NM_001354689.3:c.960G>T	NP_001341618.1:p.Leu320=
NM_001354690.2:c.900G>T	NP_001341619.1:p.Leu300=
NM_001354691.2:c.657G>T	NP_001341620.1:p.Leu219=
NM_001354692.2:c.657G>T	NP_001341621.1:p.Leu219=
NM_001354693.2:c.801G>T	NP_001341622.1:p.Leu267=
NM_001354694.2:c.717G>T	NP_001341623.1:p.Leu239=
NM_001354695.2:c.558G>T	NP_001341624.1:p.Leu186=
NR_148940.2:n.1231G>T
NR_148941.2:n.1231G>T
NR_148942.2:n.1231G>T
NM_001354690.3:c.900G>T	NP_001341619.1:p.Leu300=
NM_001354691.3:c.657G>T	NP_001341620.1:p.Leu219=
NM_001354692.3:c.657G>T	NP_001341621.1:p.Leu219=
NM_001354693.3:c.801G>T	NP_001341622.1:p.Leu267=
NM_001354694.3:c.717G>T	NP_001341623.1:p.Leu239=
NM_001354695.3:c.558G>T	NP_001341624.1:p.Leu186=
NM_002880.4:c.900G>T MANE Select	NP_002871.1:p.Leu300=
NR_148940.3:n.1231G>T
NR_148941.3:n.1231G>T
NR_148942.3:n.1231G>T