Canonical Allele Identifier: CA351508971

Gene: RAF1

Linked Data

• dbSNP Id: rs2125380554
• MyVariant Identifiers: chr3:g.12641722G>A (hg19) ; chr3:g.12600223G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12600223G>A , CM000665.2:g.12600223G>A	GRCh38
NC_000003.11:g.12641722G>A , CM000665.1:g.12641722G>A	GRCh37
NC_000003.10:g.12616722G>A	NCBI36
NG_007467.1:g.68957C>T , LRG_413:g.68957C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*584C>T	ENSP00000401088.1:n.*584C>T
ENST00000432427.3:c.239C>T
ENST00000465826.6:n.510C>T
ENST00000491290.2:n.1296C>T
ENST00000684903.1:c.*596C>T	ENSP00000508612.1:n.*596C>T
ENST00000685348.1:c.*596C>T	ENSP00000510285.1:n.*596C>T
ENST00000685437.1:c.820C>T	ENSP00000508794.1:p.Gln274Ter
ENST00000685438.1:n.683C>T
ENST00000685653.1:c.919C>T	ENSP00000509968.1:p.Gln307Ter
ENST00000685738.1:c.919C>T	ENSP00000510156.1:p.Gln307Ter
ENST00000686409.1:n.1627C>T
ENST00000686455.1:n.1282C>T
ENST00000686479.1:n.1290C>T
ENST00000686762.1:c.919C>T	ENSP00000509767.1:p.Gln307Ter
ENST00000687257.1:n.1155C>T
ENST00000687326.1:c.919C>T	ENSP00000509665.1:p.Gln307Ter
ENST00000687486.1:c.182+165C>T
ENST00000687505.1:n.1037C>T
ENST00000687923.1:c.820C>T	ENSP00000510255.1:p.Gln274Ter
ENST00000687940.1:n.1296C>T
ENST00000688269.1:n.1515C>T
ENST00000688326.1:c.239C>T
ENST00000688444.1:n.1245C>T
ENST00000688543.1:c.820C>T	ENSP00000509612.1:p.Gln274Ter
ENST00000688625.1:c.*497C>T	ENSP00000509522.1:n.*497C>T
ENST00000688803.1:n.1150C>T
ENST00000689097.1:c.*596C>T	ENSP00000509756.1:n.*596C>T
ENST00000689389.1:c.919C>T	ENSP00000510213.1:p.Gln307Ter
ENST00000689418.1:c.*596C>T	ENSP00000509467.1:n.*596C>T
ENST00000689481.1:c.*596C>T	ENSP00000510248.1:n.*596C>T
ENST00000689540.1:n.1069C>T
ENST00000689876.1:c.919C>T	ENSP00000508535.1:p.Gln307Ter
ENST00000689914.1:c.919C>T	ENSP00000509847.1:p.Gln307Ter
ENST00000690397.1:c.808C>T	ENSP00000508730.1:p.Gln270Ter
ENST00000690460.1:c.907C>T	ENSP00000509106.1:p.Gln303Ter
ENST00000690625.1:n.1222C>T
ENST00000691268.1:c.346C>T
ENST00000691396.1:c.*712C>T	ENSP00000510712.1:n.*712C>T
ENST00000691724.1:c.919C>T	ENSP00000509255.1:p.Gln307Ter
ENST00000691779.1:c.*497C>T	ENSP00000508592.1:n.*497C>T
ENST00000691899.1:c.919C>T	ENSP00000508763.1:p.Gln307Ter
ENST00000692069.1:n.1142C>T
ENST00000692093.1:c.820C>T	ENSP00000509669.1:p.Gln274Ter
ENST00000692311.1:n.1400C>T
ENST00000692558.1:n.1284C>T
ENST00000692773.1:c.*656C>T	ENSP00000509055.1:n.*656C>T
ENST00000692830.1:c.*664C>T	ENSP00000509461.1:n.*664C>T
ENST00000693069.1:c.820C>T	ENSP00000510072.1:p.Gln274Ter
ENST00000693312.1:c.694C>T	ENSP00000508686.1:p.Gln232Ter
ENST00000693664.1:c.919C>T	ENSP00000509614.1:p.Gln307Ter
ENST00000693705.1:c.*596C>T	ENSP00000510697.1:n.*596C>T
ENST00000251849.9:c.919C>T MANE Select	ENSP00000251849.4:p.Gln307Ter
ENST00000442415.7:c.979C>T	ENSP00000401888.2:p.Gln327Ter
ENST00000251849.8:c.919C>T	ENSP00000251849.4:p.Gln307Ter
ENST00000423275.5:c.*596C>T	ENSP00000401088.1:n.*596C>T
ENST00000432427.2:c.556C>T	ENSP00000398591.2:p.Gln186Ter
ENST00000442415.6:c.979C>T	ENSP00000401888.2:p.Gln327Ter
ENST00000465826.5:n.163C>T
ENST00000491290.1:n.548C>T
NM_002880.3:c.919C>T , LRG_413t1:c.919C>T	NP_002871.1:p.Gln307Ter
XM_005265355.1:c.919C>T	XP_005265412.1:p.Gln307Ter
XM_005265357.1:c.820C>T	XP_005265414.1:p.Gln274Ter
XM_005265358.3:c.676C>T	XP_005265415.1:p.Gln226Ter
XM_005265359.3:c.577C>T	XP_005265416.1:p.Gln193Ter
XM_005265360.1:c.919C>T	XP_005265417.1:p.Gln307Ter
XM_011533974.1:c.919C>T	XP_011532276.1:p.Gln307Ter
XM_011533975.1:c.676C>T	XP_011532277.1:p.Gln226Ter
NM_001354689.1:c.979C>T	NP_001341618.1:p.Gln327Ter
NM_001354690.1:c.919C>T	NP_001341619.1:p.Gln307Ter
NM_001354691.1:c.676C>T	NP_001341620.1:p.Gln226Ter
NM_001354692.1:c.676C>T	NP_001341621.1:p.Gln226Ter
NM_001354693.1:c.820C>T	NP_001341622.1:p.Gln274Ter
NM_001354694.1:c.736C>T	NP_001341623.1:p.Gln246Ter
NM_001354695.1:c.577C>T	NP_001341624.1:p.Gln193Ter
NR_148940.1:n.1334C>T
NR_148941.1:n.1334C>T
NR_148942.1:n.1334C>T
XM_011533974.3:c.919C>T	XP_011532276.1:p.Gln307Ter
XM_017006966.1:c.820C>T	XP_016862455.1:p.Gln274Ter
XR_001740227.1:n.1151C>T
NM_001354689.3:c.979C>T	NP_001341618.1:p.Gln327Ter
NM_001354690.2:c.919C>T	NP_001341619.1:p.Gln307Ter
NM_001354691.2:c.676C>T	NP_001341620.1:p.Gln226Ter
NM_001354692.2:c.676C>T	NP_001341621.1:p.Gln226Ter
NM_001354693.2:c.820C>T	NP_001341622.1:p.Gln274Ter
NM_001354694.2:c.736C>T	NP_001341623.1:p.Gln246Ter
NM_001354695.2:c.577C>T	NP_001341624.1:p.Gln193Ter
NR_148940.2:n.1250C>T
NR_148941.2:n.1250C>T
NR_148942.2:n.1250C>T
NM_001354690.3:c.919C>T	NP_001341619.1:p.Gln307Ter
NM_001354691.3:c.676C>T	NP_001341620.1:p.Gln226Ter
NM_001354692.3:c.676C>T	NP_001341621.1:p.Gln226Ter
NM_001354693.3:c.820C>T	NP_001341622.1:p.Gln274Ter
NM_001354694.3:c.736C>T	NP_001341623.1:p.Gln246Ter
NM_001354695.3:c.577C>T	NP_001341624.1:p.Gln193Ter
NM_002880.4:c.919C>T MANE Select	NP_002871.1:p.Gln307Ter
NR_148940.3:n.1250C>T
NR_148941.3:n.1250C>T
NR_148942.3:n.1250C>T