Canonical Allele Identifier: CA351502179

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632395G>T (hg19) ; chr3:g.12590896G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590896G>T , CM000665.2:g.12590896G>T	GRCh38
NC_000003.11:g.12632395G>T , CM000665.1:g.12632395G>T	GRCh37
NC_000003.10:g.12607395G>T	NCBI36
NG_007467.1:g.78284C>A , LRG_413:g.78284C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*937C>A	ENSP00000401088.1:n.*937C>A
ENST00000432427.3:c.589C>A
ENST00000460610.2:n.66C>A
ENST00000465826.6:n.863C>A
ENST00000475353.2:n.1194C>A
ENST00000494557.2:n.1083C>A
ENST00000684903.1:c.*949C>A	ENSP00000508612.1:n.*949C>A
ENST00000685348.1:c.*949C>A	ENSP00000510285.1:n.*949C>A
ENST00000685437.1:c.1173C>A	ENSP00000508794.1:p.Cys391Ter
ENST00000685653.1:c.1272C>A	ENSP00000509968.1:p.Cys424Ter
ENST00000685738.1:c.*236C>A	ENSP00000510156.1:n.*236C>A
ENST00000686409.1:n.2323C>A
ENST00000686455.1:n.1635C>A
ENST00000686762.1:c.1272C>A	ENSP00000509767.1:p.Cys424Ter
ENST00000687257.1:n.1508C>A
ENST00000687326.1:c.*206C>A	ENSP00000509665.1:n.*206C>A
ENST00000687505.1:n.1390C>A
ENST00000687923.1:c.1161C>A	ENSP00000510255.1:p.Cys387Ter
ENST00000687940.1:n.1649C>A
ENST00000688269.1:n.1868C>A
ENST00000688326.1:c.705C>A
ENST00000688444.1:n.1598C>A
ENST00000688543.1:c.1173C>A	ENSP00000509612.1:p.Cys391Ter
ENST00000688625.1:c.*850C>A	ENSP00000509522.1:n.*850C>A
ENST00000688803.1:n.1503C>A
ENST00000688914.1:n.258C>A
ENST00000689097.1:c.*949C>A	ENSP00000509756.1:n.*949C>A
ENST00000689389.1:c.1193+812C>A	ENSP00000510213.1:n.1193+812C>A
ENST00000689418.1:c.*949C>A	ENSP00000509467.1:n.*949C>A
ENST00000689481.1:c.*949C>A	ENSP00000510248.1:n.*949C>A
ENST00000689540.1:n.1422C>A
ENST00000689876.1:c.1272C>A	ENSP00000508535.1:p.Cys424Ter
ENST00000689914.1:c.*206C>A	ENSP00000509847.1:n.*206C>A
ENST00000690397.1:c.1161C>A	ENSP00000508730.1:p.Cys387Ter
ENST00000690460.1:c.1260C>A	ENSP00000509106.1:p.Cys420Ter
ENST00000690585.1:c.164C>A
ENST00000690625.1:n.2308C>A
ENST00000691396.1:c.*1124C>A	ENSP00000510712.1:n.*1124C>A
ENST00000691724.1:c.*229C>A	ENSP00000509255.1:n.*229C>A
ENST00000691779.1:c.*850C>A	ENSP00000508592.1:n.*850C>A
ENST00000691888.1:c.164C>A
ENST00000691899.1:c.1272C>A	ENSP00000508763.1:p.Cys424Ter
ENST00000692069.1:n.1838C>A
ENST00000692093.1:c.1173C>A	ENSP00000509669.1:p.Cys391Ter
ENST00000692311.1:n.2096C>A
ENST00000692558.1:n.1637C>A
ENST00000692773.1:c.*1009C>A	ENSP00000509055.1:n.*1009C>A
ENST00000692830.1:c.*1017C>A	ENSP00000509461.1:n.*1017C>A
ENST00000693069.1:c.*206C>A	ENSP00000510072.1:n.*206C>A
ENST00000693312.1:c.1047C>A	ENSP00000508686.1:p.Cys349Ter
ENST00000693664.1:c.1272C>A	ENSP00000509614.1:p.Cys424Ter
ENST00000693705.1:c.*949C>A	ENSP00000510697.1:n.*949C>A
ENST00000251849.9:c.1272C>A MANE Select	ENSP00000251849.4:p.Cys424Ter
ENST00000442415.7:c.1332C>A	ENSP00000401888.2:p.Cys444Ter
ENST00000251849.8:c.1272C>A	ENSP00000251849.4:p.Cys424Ter
ENST00000423275.5:c.*949C>A	ENSP00000401088.1:n.*949C>A
ENST00000432427.2:c.909C>A	ENSP00000398591.2:p.Cys303Ter
ENST00000442415.6:c.1332C>A	ENSP00000401888.2:p.Cys444Ter
ENST00000460610.1:n.229C>A
ENST00000465826.5:n.629C>A
ENST00000475353.1:n.440C>A
ENST00000494557.1:n.288C>A
NM_002880.3:c.1272C>A , LRG_413t1:c.1272C>A	NP_002871.1:p.Cys424Ter
XM_005265355.1:c.1272C>A	XP_005265412.1:p.Cys424Ter
XM_005265357.1:c.1173C>A	XP_005265414.1:p.Cys391Ter
XM_005265358.3:c.1029C>A	XP_005265415.1:p.Cys343Ter
XM_005265359.3:c.930C>A	XP_005265416.1:p.Cys310Ter
XM_005265360.1:c.1272C>A	XP_005265417.1:p.Cys424Ter
XM_011533974.1:c.1272C>A	XP_011532276.1:p.Cys424Ter
XM_011533975.1:c.1029C>A	XP_011532277.1:p.Cys343Ter
NM_001354689.1:c.1332C>A	NP_001341618.1:p.Cys444Ter
NM_001354690.1:c.1272C>A	NP_001341619.1:p.Cys424Ter
NM_001354691.1:c.1029C>A	NP_001341620.1:p.Cys343Ter
NM_001354692.1:c.1029C>A	NP_001341621.1:p.Cys343Ter
NM_001354693.1:c.1173C>A	NP_001341622.1:p.Cys391Ter
NM_001354694.1:c.1089C>A	NP_001341623.1:p.Cys363Ter
NM_001354695.1:c.930C>A	NP_001341624.1:p.Cys310Ter
NR_148940.1:n.1800C>A
NR_148941.1:n.1746C>A
NR_148942.1:n.1685C>A
XM_011533974.3:c.1272C>A	XP_011532276.1:p.Cys424Ter
XM_017006966.1:c.1173C>A	XP_016862455.1:p.Cys391Ter
NM_001354689.3:c.1332C>A	NP_001341618.1:p.Cys444Ter
NM_001354690.2:c.1272C>A	NP_001341619.1:p.Cys424Ter
NM_001354691.2:c.1029C>A	NP_001341620.1:p.Cys343Ter
NM_001354692.2:c.1029C>A	NP_001341621.1:p.Cys343Ter
NM_001354693.2:c.1173C>A	NP_001341622.1:p.Cys391Ter
NM_001354694.2:c.1089C>A	NP_001341623.1:p.Cys363Ter
NM_001354695.2:c.930C>A	NP_001341624.1:p.Cys310Ter
NR_148940.2:n.1716C>A
NR_148941.2:n.1662C>A
NR_148942.2:n.1601C>A
NM_001354690.3:c.1272C>A	NP_001341619.1:p.Cys424Ter
NM_001354691.3:c.1029C>A	NP_001341620.1:p.Cys343Ter
NM_001354692.3:c.1029C>A	NP_001341621.1:p.Cys343Ter
NM_001354693.3:c.1173C>A	NP_001341622.1:p.Cys391Ter
NM_001354694.3:c.1089C>A	NP_001341623.1:p.Cys363Ter
NM_001354695.3:c.930C>A	NP_001341624.1:p.Cys310Ter
NM_002880.4:c.1272C>A MANE Select	NP_002871.1:p.Cys424Ter
NR_148940.3:n.1716C>A
NR_148941.3:n.1662C>A
NR_148942.3:n.1601C>A