Canonical Allele Identifier: CA351502312

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632415C>A (hg19) ; chr3:g.12590916C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590916C>A , CM000665.2:g.12590916C>A	GRCh38
NC_000003.11:g.12632415C>A , CM000665.1:g.12632415C>A	GRCh37
NC_000003.10:g.12607415C>A	NCBI36
NG_007467.1:g.78264G>T , LRG_413:g.78264G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*917G>T	ENSP00000401088.1:n.*917G>T
ENST00000432427.3:c.569G>T
ENST00000460610.2:n.46G>T
ENST00000465826.6:n.843G>T
ENST00000475353.2:n.1174G>T
ENST00000494557.2:n.1063G>T
ENST00000684903.1:c.*929G>T	ENSP00000508612.1:n.*929G>T
ENST00000685348.1:c.*929G>T	ENSP00000510285.1:n.*929G>T
ENST00000685437.1:c.1153G>T	ENSP00000508794.1:p.Ala385Ser
ENST00000685653.1:c.1252G>T	ENSP00000509968.1:p.Ala418Ser
ENST00000685738.1:c.*216G>T	ENSP00000510156.1:n.*216G>T
ENST00000686409.1:n.2303G>T
ENST00000686455.1:n.1615G>T
ENST00000686762.1:c.1252G>T	ENSP00000509767.1:p.Ala418Ser
ENST00000687257.1:n.1488G>T
ENST00000687326.1:c.*186G>T	ENSP00000509665.1:n.*186G>T
ENST00000687505.1:n.1370G>T
ENST00000687923.1:c.1141G>T	ENSP00000510255.1:p.Ala381Ser
ENST00000687940.1:n.1629G>T
ENST00000688269.1:n.1848G>T
ENST00000688326.1:c.685G>T
ENST00000688444.1:n.1578G>T
ENST00000688543.1:c.1153G>T	ENSP00000509612.1:p.Ala385Ser
ENST00000688625.1:c.*830G>T	ENSP00000509522.1:n.*830G>T
ENST00000688803.1:n.1483G>T
ENST00000688914.1:n.238G>T
ENST00000689097.1:c.*929G>T	ENSP00000509756.1:n.*929G>T
ENST00000689389.1:c.1193+792G>T	ENSP00000510213.1:n.1193+792G>T
ENST00000689418.1:c.*929G>T	ENSP00000509467.1:n.*929G>T
ENST00000689481.1:c.*929G>T	ENSP00000510248.1:n.*929G>T
ENST00000689540.1:n.1402G>T
ENST00000689876.1:c.1252G>T	ENSP00000508535.1:p.Ala418Ser
ENST00000689914.1:c.*186G>T	ENSP00000509847.1:n.*186G>T
ENST00000690397.1:c.1141G>T	ENSP00000508730.1:p.Ala381Ser
ENST00000690460.1:c.1240G>T	ENSP00000509106.1:p.Ala414Ser
ENST00000690585.1:c.144G>T
ENST00000690625.1:n.2288G>T
ENST00000691396.1:c.*1104G>T	ENSP00000510712.1:n.*1104G>T
ENST00000691724.1:c.*209G>T	ENSP00000509255.1:n.*209G>T
ENST00000691779.1:c.*830G>T	ENSP00000508592.1:n.*830G>T
ENST00000691888.1:c.144G>T
ENST00000691899.1:c.1252G>T	ENSP00000508763.1:p.Ala418Ser
ENST00000692069.1:n.1818G>T
ENST00000692093.1:c.1153G>T	ENSP00000509669.1:p.Ala385Ser
ENST00000692311.1:n.2076G>T
ENST00000692558.1:n.1617G>T
ENST00000692773.1:c.*989G>T	ENSP00000509055.1:n.*989G>T
ENST00000692830.1:c.*997G>T	ENSP00000509461.1:n.*997G>T
ENST00000693069.1:c.*186G>T	ENSP00000510072.1:n.*186G>T
ENST00000693312.1:c.1027G>T	ENSP00000508686.1:p.Ala343Ser
ENST00000693664.1:c.1252G>T	ENSP00000509614.1:p.Ala418Ser
ENST00000693705.1:c.*929G>T	ENSP00000510697.1:n.*929G>T
ENST00000251849.9:c.1252G>T MANE Select	ENSP00000251849.4:p.Ala418Ser
ENST00000442415.7:c.1312G>T	ENSP00000401888.2:p.Ala438Ser
ENST00000251849.8:c.1252G>T	ENSP00000251849.4:p.Ala418Ser
ENST00000423275.5:c.*929G>T	ENSP00000401088.1:n.*929G>T
ENST00000432427.2:c.889G>T	ENSP00000398591.2:p.Ala297Ser
ENST00000442415.6:c.1312G>T	ENSP00000401888.2:p.Ala438Ser
ENST00000460610.1:n.209G>T
ENST00000465826.5:n.609G>T
ENST00000475353.1:n.420G>T
ENST00000494557.1:n.268G>T
NM_002880.3:c.1252G>T , LRG_413t1:c.1252G>T	NP_002871.1:p.Ala418Ser
XM_005265355.1:c.1252G>T	XP_005265412.1:p.Ala418Ser
XM_005265357.1:c.1153G>T	XP_005265414.1:p.Ala385Ser
XM_005265358.3:c.1009G>T	XP_005265415.1:p.Ala337Ser
XM_005265359.3:c.910G>T	XP_005265416.1:p.Ala304Ser
XM_005265360.1:c.1252G>T	XP_005265417.1:p.Ala418Ser
XM_011533974.1:c.1252G>T	XP_011532276.1:p.Ala418Ser
XM_011533975.1:c.1009G>T	XP_011532277.1:p.Ala337Ser
NM_001354689.1:c.1312G>T	NP_001341618.1:p.Ala438Ser
NM_001354690.1:c.1252G>T	NP_001341619.1:p.Ala418Ser
NM_001354691.1:c.1009G>T	NP_001341620.1:p.Ala337Ser
NM_001354692.1:c.1009G>T	NP_001341621.1:p.Ala337Ser
NM_001354693.1:c.1153G>T	NP_001341622.1:p.Ala385Ser
NM_001354694.1:c.1069G>T	NP_001341623.1:p.Ala357Ser
NM_001354695.1:c.910G>T	NP_001341624.1:p.Ala304Ser
NR_148940.1:n.1780G>T
NR_148941.1:n.1726G>T
NR_148942.1:n.1665G>T
XM_011533974.3:c.1252G>T	XP_011532276.1:p.Ala418Ser
XM_017006966.1:c.1153G>T	XP_016862455.1:p.Ala385Ser
NM_001354689.3:c.1312G>T	NP_001341618.1:p.Ala438Ser
NM_001354690.2:c.1252G>T	NP_001341619.1:p.Ala418Ser
NM_001354691.2:c.1009G>T	NP_001341620.1:p.Ala337Ser
NM_001354692.2:c.1009G>T	NP_001341621.1:p.Ala337Ser
NM_001354693.2:c.1153G>T	NP_001341622.1:p.Ala385Ser
NM_001354694.2:c.1069G>T	NP_001341623.1:p.Ala357Ser
NM_001354695.2:c.910G>T	NP_001341624.1:p.Ala304Ser
NR_148940.2:n.1696G>T
NR_148941.2:n.1642G>T
NR_148942.2:n.1581G>T
NM_001354690.3:c.1252G>T	NP_001341619.1:p.Ala418Ser
NM_001354691.3:c.1009G>T	NP_001341620.1:p.Ala337Ser
NM_001354692.3:c.1009G>T	NP_001341621.1:p.Ala337Ser
NM_001354693.3:c.1153G>T	NP_001341622.1:p.Ala385Ser
NM_001354694.3:c.1069G>T	NP_001341623.1:p.Ala357Ser
NM_001354695.3:c.910G>T	NP_001341624.1:p.Ala304Ser
NM_002880.4:c.1252G>T MANE Select	NP_002871.1:p.Ala418Ser
NR_148940.3:n.1696G>T
NR_148941.3:n.1642G>T
NR_148942.3:n.1581G>T