Canonical Allele Identifier: CA351501891

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632350C>A (hg19) ; chr3:g.12590851C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590851C>A , CM000665.2:g.12590851C>A	GRCh38
NC_000003.11:g.12632350C>A , CM000665.1:g.12632350C>A	GRCh37
NC_000003.10:g.12607350C>A	NCBI36
NG_007467.1:g.78329G>T , LRG_413:g.78329G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*982G>T	ENSP00000401088.1:n.*982G>T
ENST00000432427.3:c.634G>T
ENST00000460610.2:n.111G>T
ENST00000465826.6:n.908G>T
ENST00000475353.2:n.1239G>T
ENST00000494557.2:n.1128G>T
ENST00000684903.1:c.*994G>T	ENSP00000508612.1:n.*994G>T
ENST00000685348.1:c.*994G>T	ENSP00000510285.1:n.*994G>T
ENST00000685437.1:c.1218G>T	ENSP00000508794.1:p.Lys406Asn
ENST00000685653.1:c.1317G>T	ENSP00000509968.1:p.Lys439Asn
ENST00000685738.1:c.*281G>T	ENSP00000510156.1:n.*281G>T
ENST00000686409.1:n.2368G>T
ENST00000686455.1:n.1680G>T
ENST00000686762.1:c.1317G>T	ENSP00000509767.1:p.Lys439Asn
ENST00000687257.1:n.1553G>T
ENST00000687326.1:c.*251G>T	ENSP00000509665.1:n.*251G>T
ENST00000687505.1:n.1435G>T
ENST00000687923.1:c.1206G>T	ENSP00000510255.1:p.Lys402Asn
ENST00000687940.1:n.1694G>T
ENST00000688269.1:n.1913G>T
ENST00000688326.1:c.750G>T
ENST00000688444.1:n.1643G>T
ENST00000688543.1:c.1218G>T	ENSP00000509612.1:p.Lys406Asn
ENST00000688625.1:c.*895G>T	ENSP00000509522.1:n.*895G>T
ENST00000688803.1:n.1548G>T
ENST00000688914.1:n.303G>T
ENST00000689097.1:c.*994G>T	ENSP00000509756.1:n.*994G>T
ENST00000689389.1:c.1193+857G>T	ENSP00000510213.1:n.1193+857G>T
ENST00000689418.1:c.*994G>T	ENSP00000509467.1:n.*994G>T
ENST00000689481.1:c.*994G>T	ENSP00000510248.1:n.*994G>T
ENST00000689540.1:n.1467G>T
ENST00000689876.1:c.1317G>T	ENSP00000508535.1:p.Lys439Asn
ENST00000689914.1:c.*251G>T	ENSP00000509847.1:n.*251G>T
ENST00000690397.1:c.1206G>T	ENSP00000508730.1:p.Lys402Asn
ENST00000690460.1:c.1305G>T	ENSP00000509106.1:p.Lys435Asn
ENST00000690585.1:c.209G>T
ENST00000690625.1:n.2353G>T
ENST00000691396.1:c.*1169G>T	ENSP00000510712.1:n.*1169G>T
ENST00000691724.1:c.*274G>T	ENSP00000509255.1:n.*274G>T
ENST00000691779.1:c.*895G>T	ENSP00000508592.1:n.*895G>T
ENST00000691888.1:c.209G>T
ENST00000691899.1:c.1317G>T	ENSP00000508763.1:p.Lys439Asn
ENST00000692069.1:n.1883G>T
ENST00000692093.1:c.1218G>T	ENSP00000509669.1:p.Lys406Asn
ENST00000692311.1:n.2141G>T
ENST00000692558.1:n.1682G>T
ENST00000692773.1:c.*1054G>T	ENSP00000509055.1:n.*1054G>T
ENST00000692830.1:c.*1062G>T	ENSP00000509461.1:n.*1062G>T
ENST00000693069.1:c.*251G>T	ENSP00000510072.1:n.*251G>T
ENST00000693312.1:c.1092G>T	ENSP00000508686.1:p.Lys364Asn
ENST00000693664.1:c.1317G>T	ENSP00000509614.1:p.Lys439Asn
ENST00000693705.1:c.*994G>T	ENSP00000510697.1:n.*994G>T
ENST00000251849.9:c.1317G>T MANE Select	ENSP00000251849.4:p.Lys439Asn
ENST00000442415.7:c.1377G>T	ENSP00000401888.2:p.Lys459Asn
ENST00000251849.8:c.1317G>T	ENSP00000251849.4:p.Lys439Asn
ENST00000423275.5:c.*994G>T	ENSP00000401088.1:n.*994G>T
ENST00000432427.2:c.954G>T	ENSP00000398591.2:p.Lys318Asn
ENST00000442415.6:c.1377G>T	ENSP00000401888.2:p.Lys459Asn
ENST00000460610.1:n.274G>T
ENST00000465826.5:n.674G>T
ENST00000475353.1:n.485G>T
ENST00000494557.1:n.333G>T
NM_002880.3:c.1317G>T , LRG_413t1:c.1317G>T	NP_002871.1:p.Lys439Asn
XM_005265355.1:c.1317G>T	XP_005265412.1:p.Lys439Asn
XM_005265357.1:c.1218G>T	XP_005265414.1:p.Lys406Asn
XM_005265358.3:c.1074G>T	XP_005265415.1:p.Lys358Asn
XM_005265359.3:c.975G>T	XP_005265416.1:p.Lys325Asn
XM_005265360.1:c.1317G>T	XP_005265417.1:p.Lys439Asn
XM_011533974.1:c.1317G>T	XP_011532276.1:p.Lys439Asn
XM_011533975.1:c.1074G>T	XP_011532277.1:p.Lys358Asn
NM_001354689.1:c.1377G>T	NP_001341618.1:p.Lys459Asn
NM_001354690.1:c.1317G>T	NP_001341619.1:p.Lys439Asn
NM_001354691.1:c.1074G>T	NP_001341620.1:p.Lys358Asn
NM_001354692.1:c.1074G>T	NP_001341621.1:p.Lys358Asn
NM_001354693.1:c.1218G>T	NP_001341622.1:p.Lys406Asn
NM_001354694.1:c.1134G>T	NP_001341623.1:p.Lys378Asn
NM_001354695.1:c.975G>T	NP_001341624.1:p.Lys325Asn
NR_148940.1:n.1845G>T
NR_148941.1:n.1791G>T
NR_148942.1:n.1730G>T
XM_011533974.3:c.1317G>T	XP_011532276.1:p.Lys439Asn
XM_017006966.1:c.1218G>T	XP_016862455.1:p.Lys406Asn
NM_001354689.3:c.1377G>T	NP_001341618.1:p.Lys459Asn
NM_001354690.2:c.1317G>T	NP_001341619.1:p.Lys439Asn
NM_001354691.2:c.1074G>T	NP_001341620.1:p.Lys358Asn
NM_001354692.2:c.1074G>T	NP_001341621.1:p.Lys358Asn
NM_001354693.2:c.1218G>T	NP_001341622.1:p.Lys406Asn
NM_001354694.2:c.1134G>T	NP_001341623.1:p.Lys378Asn
NM_001354695.2:c.975G>T	NP_001341624.1:p.Lys325Asn
NR_148940.2:n.1761G>T
NR_148941.2:n.1707G>T
NR_148942.2:n.1646G>T
NM_001354690.3:c.1317G>T	NP_001341619.1:p.Lys439Asn
NM_001354691.3:c.1074G>T	NP_001341620.1:p.Lys358Asn
NM_001354692.3:c.1074G>T	NP_001341621.1:p.Lys358Asn
NM_001354693.3:c.1218G>T	NP_001341622.1:p.Lys406Asn
NM_001354694.3:c.1134G>T	NP_001341623.1:p.Lys378Asn
NM_001354695.3:c.975G>T	NP_001341624.1:p.Lys325Asn
NM_002880.4:c.1317G>T MANE Select	NP_002871.1:p.Lys439Asn
NR_148940.3:n.1761G>T
NR_148941.3:n.1707G>T
NR_148942.3:n.1646G>T