Canonical Allele Identifier: CA351501680

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632309G>T (hg19) ; chr3:g.12590810G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590810G>T , CM000665.2:g.12590810G>T	GRCh38
NC_000003.11:g.12632309G>T , CM000665.1:g.12632309G>T	GRCh37
NC_000003.10:g.12607309G>T	NCBI36
NG_007467.1:g.78370C>A , LRG_413:g.78370C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1023C>A	ENSP00000401088.1:n.*1023C>A
ENST00000432427.3:c.675C>A
ENST00000460610.2:n.152C>A
ENST00000465826.6:n.949C>A
ENST00000475353.2:n.1280C>A
ENST00000494557.2:n.1169C>A
ENST00000684903.1:c.*1035C>A	ENSP00000508612.1:n.*1035C>A
ENST00000685348.1:c.*1035C>A	ENSP00000510285.1:n.*1035C>A
ENST00000685437.1:c.1259C>A	ENSP00000508794.1:p.Ala420Asp
ENST00000685653.1:c.1358C>A	ENSP00000509968.1:p.Ala453Asp
ENST00000685738.1:c.*322C>A	ENSP00000510156.1:n.*322C>A
ENST00000686409.1:n.2409C>A
ENST00000686455.1:n.1721C>A
ENST00000686762.1:c.1358C>A	ENSP00000509767.1:p.Ala453Asp
ENST00000687257.1:n.1594C>A
ENST00000687326.1:c.*292C>A	ENSP00000509665.1:n.*292C>A
ENST00000687505.1:n.1476C>A
ENST00000687923.1:c.1247C>A	ENSP00000510255.1:p.Ala416Asp
ENST00000687940.1:n.1735C>A
ENST00000688269.1:n.1954C>A
ENST00000688326.1:c.791C>A
ENST00000688444.1:n.1684C>A
ENST00000688543.1:c.1259C>A	ENSP00000509612.1:p.Ala420Asp
ENST00000688625.1:c.*936C>A	ENSP00000509522.1:n.*936C>A
ENST00000688803.1:n.1589C>A
ENST00000688914.1:n.344C>A
ENST00000689097.1:c.*1035C>A	ENSP00000509756.1:n.*1035C>A
ENST00000689389.1:c.1193+898C>A	ENSP00000510213.1:n.1193+898C>A
ENST00000689418.1:c.*1035C>A	ENSP00000509467.1:n.*1035C>A
ENST00000689481.1:c.*1035C>A	ENSP00000510248.1:n.*1035C>A
ENST00000689540.1:n.1508C>A
ENST00000689876.1:c.1358C>A	ENSP00000508535.1:p.Ala453Asp
ENST00000689914.1:c.*292C>A	ENSP00000509847.1:n.*292C>A
ENST00000690397.1:c.1247C>A	ENSP00000508730.1:p.Ala416Asp
ENST00000690460.1:c.1346C>A	ENSP00000509106.1:p.Ala449Asp
ENST00000690585.1:c.250C>A
ENST00000690625.1:n.2394C>A
ENST00000691396.1:c.*1210C>A	ENSP00000510712.1:n.*1210C>A
ENST00000691724.1:c.*315C>A	ENSP00000509255.1:n.*315C>A
ENST00000691779.1:c.*936C>A	ENSP00000508592.1:n.*936C>A
ENST00000691888.1:c.250C>A
ENST00000691899.1:c.1358C>A	ENSP00000508763.1:p.Ala453Asp
ENST00000692069.1:n.1924C>A
ENST00000692093.1:c.1259C>A	ENSP00000509669.1:p.Ala420Asp
ENST00000692311.1:n.2182C>A
ENST00000692558.1:n.1723C>A
ENST00000692773.1:c.*1095C>A	ENSP00000509055.1:n.*1095C>A
ENST00000692830.1:c.*1103C>A	ENSP00000509461.1:n.*1103C>A
ENST00000693069.1:c.*292C>A	ENSP00000510072.1:n.*292C>A
ENST00000693312.1:c.1133C>A	ENSP00000508686.1:p.Ala378Asp
ENST00000693664.1:c.1358C>A	ENSP00000509614.1:p.Ala453Asp
ENST00000693705.1:c.*1035C>A	ENSP00000510697.1:n.*1035C>A
ENST00000251849.9:c.1358C>A MANE Select	ENSP00000251849.4:p.Ala453Asp
ENST00000442415.7:c.1418C>A	ENSP00000401888.2:p.Ala473Asp
ENST00000251849.8:c.1358C>A	ENSP00000251849.4:p.Ala453Asp
ENST00000423275.5:c.*1035C>A	ENSP00000401088.1:n.*1035C>A
ENST00000432427.2:c.995C>A	ENSP00000398591.2:p.Ala332Asp
ENST00000442415.6:c.1418C>A	ENSP00000401888.2:p.Ala473Asp
ENST00000460610.1:n.315C>A
ENST00000465826.5:n.715C>A
ENST00000475353.1:n.526C>A
ENST00000494557.1:n.374C>A
NM_002880.3:c.1358C>A , LRG_413t1:c.1358C>A	NP_002871.1:p.Ala453Asp
XM_005265355.1:c.1358C>A	XP_005265412.1:p.Ala453Asp
XM_005265357.1:c.1259C>A	XP_005265414.1:p.Ala420Asp
XM_005265358.3:c.1115C>A	XP_005265415.1:p.Ala372Asp
XM_005265359.3:c.1016C>A	XP_005265416.1:p.Ala339Asp
XM_005265360.1:c.1358C>A	XP_005265417.1:p.Ala453Asp
XM_011533974.1:c.1358C>A	XP_011532276.1:p.Ala453Asp
XM_011533975.1:c.1115C>A	XP_011532277.1:p.Ala372Asp
NM_001354689.1:c.1418C>A	NP_001341618.1:p.Ala473Asp
NM_001354690.1:c.1358C>A	NP_001341619.1:p.Ala453Asp
NM_001354691.1:c.1115C>A	NP_001341620.1:p.Ala372Asp
NM_001354692.1:c.1115C>A	NP_001341621.1:p.Ala372Asp
NM_001354693.1:c.1259C>A	NP_001341622.1:p.Ala420Asp
NM_001354694.1:c.1175C>A	NP_001341623.1:p.Ala392Asp
NM_001354695.1:c.1016C>A	NP_001341624.1:p.Ala339Asp
NR_148940.1:n.1886C>A
NR_148941.1:n.1832C>A
NR_148942.1:n.1771C>A
XM_011533974.3:c.1358C>A	XP_011532276.1:p.Ala453Asp
XM_017006966.1:c.1259C>A	XP_016862455.1:p.Ala420Asp
NM_001354689.3:c.1418C>A	NP_001341618.1:p.Ala473Asp
NM_001354690.2:c.1358C>A	NP_001341619.1:p.Ala453Asp
NM_001354691.2:c.1115C>A	NP_001341620.1:p.Ala372Asp
NM_001354692.2:c.1115C>A	NP_001341621.1:p.Ala372Asp
NM_001354693.2:c.1259C>A	NP_001341622.1:p.Ala420Asp
NM_001354694.2:c.1175C>A	NP_001341623.1:p.Ala392Asp
NM_001354695.2:c.1016C>A	NP_001341624.1:p.Ala339Asp
NR_148940.2:n.1802C>A
NR_148941.2:n.1748C>A
NR_148942.2:n.1687C>A
NM_001354690.3:c.1358C>A	NP_001341619.1:p.Ala453Asp
NM_001354691.3:c.1115C>A	NP_001341620.1:p.Ala372Asp
NM_001354692.3:c.1115C>A	NP_001341621.1:p.Ala372Asp
NM_001354693.3:c.1259C>A	NP_001341622.1:p.Ala420Asp
NM_001354694.3:c.1175C>A	NP_001341623.1:p.Ala392Asp
NM_001354695.3:c.1016C>A	NP_001341624.1:p.Ala339Asp
NM_002880.4:c.1358C>A MANE Select	NP_002871.1:p.Ala453Asp
NR_148940.3:n.1802C>A
NR_148941.3:n.1748C>A
NR_148942.3:n.1687C>A