Canonical Allele Identifier: CA351501794

Gene: RAF1

Linked Data

• dbSNP Id: rs757591797
• MyVariant Identifiers: chr3:g.12632333A>T (hg19) ; chr3:g.12590834A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590834A>T , CM000665.2:g.12590834A>T	GRCh38
NC_000003.11:g.12632333A>T , CM000665.1:g.12632333A>T	GRCh37
NC_000003.10:g.12607333A>T	NCBI36
NG_007467.1:g.78346T>A , LRG_413:g.78346T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*999T>A	ENSP00000401088.1:n.*999T>A
ENST00000432427.3:c.651T>A
ENST00000460610.2:n.128T>A
ENST00000465826.6:n.925T>A
ENST00000475353.2:n.1256T>A
ENST00000494557.2:n.1145T>A
ENST00000684903.1:c.*1011T>A	ENSP00000508612.1:n.*1011T>A
ENST00000685348.1:c.*1011T>A	ENSP00000510285.1:n.*1011T>A
ENST00000685437.1:c.1235T>A	ENSP00000508794.1:p.Leu412Gln
ENST00000685653.1:c.1334T>A	ENSP00000509968.1:p.Leu445Gln
ENST00000685738.1:c.*298T>A	ENSP00000510156.1:n.*298T>A
ENST00000686409.1:n.2385T>A
ENST00000686455.1:n.1697T>A
ENST00000686762.1:c.1334T>A	ENSP00000509767.1:p.Leu445Gln
ENST00000687257.1:n.1570T>A
ENST00000687326.1:c.*268T>A	ENSP00000509665.1:n.*268T>A
ENST00000687505.1:n.1452T>A
ENST00000687923.1:c.1223T>A	ENSP00000510255.1:p.Leu408Gln
ENST00000687940.1:n.1711T>A
ENST00000688269.1:n.1930T>A
ENST00000688326.1:c.767T>A
ENST00000688444.1:n.1660T>A
ENST00000688543.1:c.1235T>A	ENSP00000509612.1:p.Leu412Gln
ENST00000688625.1:c.*912T>A	ENSP00000509522.1:n.*912T>A
ENST00000688803.1:n.1565T>A
ENST00000688914.1:n.320T>A
ENST00000689097.1:c.*1011T>A	ENSP00000509756.1:n.*1011T>A
ENST00000689389.1:c.1193+874T>A	ENSP00000510213.1:n.1193+874T>A
ENST00000689418.1:c.*1011T>A	ENSP00000509467.1:n.*1011T>A
ENST00000689481.1:c.*1011T>A	ENSP00000510248.1:n.*1011T>A
ENST00000689540.1:n.1484T>A
ENST00000689876.1:c.1334T>A	ENSP00000508535.1:p.Leu445Gln
ENST00000689914.1:c.*268T>A	ENSP00000509847.1:n.*268T>A
ENST00000690397.1:c.1223T>A	ENSP00000508730.1:p.Leu408Gln
ENST00000690460.1:c.1322T>A	ENSP00000509106.1:p.Leu441Gln
ENST00000690585.1:c.226T>A
ENST00000690625.1:n.2370T>A
ENST00000691396.1:c.*1186T>A	ENSP00000510712.1:n.*1186T>A
ENST00000691724.1:c.*291T>A	ENSP00000509255.1:n.*291T>A
ENST00000691779.1:c.*912T>A	ENSP00000508592.1:n.*912T>A
ENST00000691888.1:c.226T>A
ENST00000691899.1:c.1334T>A	ENSP00000508763.1:p.Leu445Gln
ENST00000692069.1:n.1900T>A
ENST00000692093.1:c.1235T>A	ENSP00000509669.1:p.Leu412Gln
ENST00000692311.1:n.2158T>A
ENST00000692558.1:n.1699T>A
ENST00000692773.1:c.*1071T>A	ENSP00000509055.1:n.*1071T>A
ENST00000692830.1:c.*1079T>A	ENSP00000509461.1:n.*1079T>A
ENST00000693069.1:c.*268T>A	ENSP00000510072.1:n.*268T>A
ENST00000693312.1:c.1109T>A	ENSP00000508686.1:p.Leu370Gln
ENST00000693664.1:c.1334T>A	ENSP00000509614.1:p.Leu445Gln
ENST00000693705.1:c.*1011T>A	ENSP00000510697.1:n.*1011T>A
ENST00000251849.9:c.1334T>A MANE Select	ENSP00000251849.4:p.Leu445Gln
ENST00000442415.7:c.1394T>A	ENSP00000401888.2:p.Leu465Gln
ENST00000251849.8:c.1334T>A	ENSP00000251849.4:p.Leu445Gln
ENST00000423275.5:c.*1011T>A	ENSP00000401088.1:n.*1011T>A
ENST00000432427.2:c.971T>A	ENSP00000398591.2:p.Leu324Gln
ENST00000442415.6:c.1394T>A	ENSP00000401888.2:p.Leu465Gln
ENST00000460610.1:n.291T>A
ENST00000465826.5:n.691T>A
ENST00000475353.1:n.502T>A
ENST00000494557.1:n.350T>A
NM_002880.3:c.1334T>A , LRG_413t1:c.1334T>A	NP_002871.1:p.Leu445Gln
XM_005265355.1:c.1334T>A	XP_005265412.1:p.Leu445Gln
XM_005265357.1:c.1235T>A	XP_005265414.1:p.Leu412Gln
XM_005265358.3:c.1091T>A	XP_005265415.1:p.Leu364Gln
XM_005265359.3:c.992T>A	XP_005265416.1:p.Leu331Gln
XM_005265360.1:c.1334T>A	XP_005265417.1:p.Leu445Gln
XM_011533974.1:c.1334T>A	XP_011532276.1:p.Leu445Gln
XM_011533975.1:c.1091T>A	XP_011532277.1:p.Leu364Gln
NM_001354689.1:c.1394T>A	NP_001341618.1:p.Leu465Gln
NM_001354690.1:c.1334T>A	NP_001341619.1:p.Leu445Gln
NM_001354691.1:c.1091T>A	NP_001341620.1:p.Leu364Gln
NM_001354692.1:c.1091T>A	NP_001341621.1:p.Leu364Gln
NM_001354693.1:c.1235T>A	NP_001341622.1:p.Leu412Gln
NM_001354694.1:c.1151T>A	NP_001341623.1:p.Leu384Gln
NM_001354695.1:c.992T>A	NP_001341624.1:p.Leu331Gln
NR_148940.1:n.1862T>A
NR_148941.1:n.1808T>A
NR_148942.1:n.1747T>A
XM_011533974.3:c.1334T>A	XP_011532276.1:p.Leu445Gln
XM_017006966.1:c.1235T>A	XP_016862455.1:p.Leu412Gln
NM_001354689.3:c.1394T>A	NP_001341618.1:p.Leu465Gln
NM_001354690.2:c.1334T>A	NP_001341619.1:p.Leu445Gln
NM_001354691.2:c.1091T>A	NP_001341620.1:p.Leu364Gln
NM_001354692.2:c.1091T>A	NP_001341621.1:p.Leu364Gln
NM_001354693.2:c.1235T>A	NP_001341622.1:p.Leu412Gln
NM_001354694.2:c.1151T>A	NP_001341623.1:p.Leu384Gln
NM_001354695.2:c.992T>A	NP_001341624.1:p.Leu331Gln
NR_148940.2:n.1778T>A
NR_148941.2:n.1724T>A
NR_148942.2:n.1663T>A
NM_001354690.3:c.1334T>A	NP_001341619.1:p.Leu445Gln
NM_001354691.3:c.1091T>A	NP_001341620.1:p.Leu364Gln
NM_001354692.3:c.1091T>A	NP_001341621.1:p.Leu364Gln
NM_001354693.3:c.1235T>A	NP_001341622.1:p.Leu412Gln
NM_001354694.3:c.1151T>A	NP_001341623.1:p.Leu384Gln
NM_001354695.3:c.992T>A	NP_001341624.1:p.Leu331Gln
NM_002880.4:c.1334T>A MANE Select	NP_002871.1:p.Leu445Gln
NR_148940.3:n.1778T>A
NR_148941.3:n.1724T>A
NR_148942.3:n.1663T>A