Canonical Allele Identifier: CA351498963

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12627212C>A (hg19) ; chr3:g.12585713C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585713C>A , CM000665.2:g.12585713C>A	GRCh38
NC_000003.11:g.12627212C>A , CM000665.1:g.12627212C>A	GRCh37
NC_000003.10:g.12602212C>A	NCBI36
NG_007467.1:g.83467G>T , LRG_413:g.83467G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1169G>T (RAF1)	ENSP00000401088.1:n.*1169G>T
ENST00000432427.3:c.821G>T (RAF1)
ENST00000460610.2:n.5249G>T (RAF1)
ENST00000471449.2:n.314G>T (RAF1)
ENST00000475353.2:n.3217G>T (RAF1)
ENST00000684903.1:c.*1181G>T (RAF1)	ENSP00000508612.1:n.*1181G>T
ENST00000685348.1:c.*1095-307G>T (RAF1)	ENSP00000510285.1:n.*1095-307G>T
ENST00000685437.1:c.1405G>T (RAF1)	ENSP00000508794.1:p.Val469Phe
ENST00000685653.1:c.1504G>T (RAF1)	ENSP00000509968.1:p.Val502Phe
ENST00000685697.1:n.2239G>T (RAF1)
ENST00000685738.1:c.*468G>T (RAF1)	ENSP00000510156.1:n.*468G>T
ENST00000686409.1:n.4346G>T (RAF1)
ENST00000686455.1:n.3658G>T (RAF1)
ENST00000686762.1:c.*63G>T (RAF1)	ENSP00000509767.1:n.*63G>T
ENST00000687257.1:n.3531G>T (RAF1)
ENST00000687326.1:c.*2229G>T (RAF1)	ENSP00000509665.1:n.*2229G>T
ENST00000687505.1:n.1622G>T (RAF1)
ENST00000687923.1:c.1393G>T (RAF1)	ENSP00000510255.1:p.Val465Phe
ENST00000688269.1:n.2100G>T (RAF1)
ENST00000688444.1:n.3621G>T (RAF1)
ENST00000688543.1:c.1405G>T (RAF1)	ENSP00000509612.1:p.Val469Phe
ENST00000688625.1:c.*2873G>T (RAF1)	ENSP00000509522.1:n.*2873G>T
ENST00000688803.1:n.2965-460G>T (RAF1)
ENST00000688914.1:n.490G>T (RAF1)
ENST00000689097.1:c.*1181G>T (RAF1)	ENSP00000509756.1:n.*1181G>T
ENST00000689389.1:c.1327G>T (RAF1)	ENSP00000510213.1:p.Val443Phe
ENST00000689418.1:c.*2972G>T (RAF1)	ENSP00000509467.1:n.*2972G>T
ENST00000689540.1:n.3445G>T (RAF1)
ENST00000689876.1:c.1418-307G>T (RAF1)	ENSP00000508535.1:n.1418-307G>T
ENST00000689914.1:c.*438G>T (RAF1)	ENSP00000509847.1:n.*438G>T
ENST00000690397.1:c.1393G>T (RAF1)	ENSP00000508730.1:p.Val465Phe
ENST00000690460.1:c.1492G>T (RAF1)	ENSP00000509106.1:p.Val498Phe
ENST00000690585.1:c.263-460G>T (RAF1)
ENST00000690625.1:n.2540G>T (RAF1)
ENST00000691396.1:c.*1376G>T (RAF1)	ENSP00000510712.1:n.*1376G>T
ENST00000691643.1:n.2130G>T (RAF1)
ENST00000691724.1:c.*461G>T (RAF1)	ENSP00000509255.1:n.*461G>T
ENST00000691779.1:c.*1082G>T (RAF1)	ENSP00000508592.1:n.*1082G>T
ENST00000691888.1:c.378G>T (RAF1)
ENST00000691899.1:c.1504G>T (RAF1)	ENSP00000508763.1:p.Val502Phe
ENST00000692069.1:n.3861G>T (RAF1)
ENST00000692093.1:c.1405G>T (RAF1)	ENSP00000509669.1:p.Val469Phe
ENST00000692311.1:n.2328G>T (RAF1)
ENST00000692558.1:n.3660G>T (RAF1)
ENST00000692773.1:c.*1241G>T (RAF1)	ENSP00000509055.1:n.*1241G>T
ENST00000692830.1:c.*1249G>T (RAF1)	ENSP00000509461.1:n.*1249G>T
ENST00000693312.1:c.1279G>T (RAF1)	ENSP00000508686.1:p.Val427Phe
ENST00000693664.1:c.1488-460G>T (RAF1)	ENSP00000509614.1:n.1488-460G>T
ENST00000693705.1:c.*1048-732G>T (RAF1)	ENSP00000510697.1:n.*1048-732G>T
ENST00000251849.9:c.1504G>T (RAF1) MANE Select	ENSP00000251849.4:p.Val502Phe
ENST00000442415.7:c.1564G>T (RAF1)	ENSP00000401888.2:p.Val522Phe
ENST00000676541.1:c.*3460C>A (MKRN2)	ENSP00000503730.1:n.*3460C>A
ENST00000677142.1:c.*3460C>A (MKRN2)	ENSP00000504455.1:n.*3460C>A
ENST00000677816.1:c.*2015C>A (MKRN2)	ENSP00000502893.1:n.*2015C>A
ENST00000677941.1:n.3523C>A (MKRN2)
ENST00000251849.8:c.1504G>T (RAF1)	ENSP00000251849.4:p.Val502Phe
ENST00000423275.5:c.*1181G>T (RAF1)	ENSP00000401088.1:n.*1181G>T
ENST00000432427.2:c.1141G>T (RAF1)	ENSP00000398591.2:p.Val381Phe
ENST00000442415.6:c.1564G>T (RAF1)	ENSP00000401888.2:p.Val522Phe
ENST00000471449.1:n.193G>T (RAF1)
NM_002880.3:c.1504G>T , LRG_413t1:c.1504G>T (RAF1)	NP_002871.1:p.Val502Phe
XM_005265355.1:c.1504G>T (RAF1)	XP_005265412.1:p.Val502Phe
XM_005265357.1:c.1405G>T (RAF1)	XP_005265414.1:p.Val469Phe
XM_005265358.3:c.1261G>T (RAF1)	XP_005265415.1:p.Val421Phe
XM_005265359.3:c.1162G>T (RAF1)	XP_005265416.1:p.Val388Phe
XM_005265360.1:c.1418-307G>T (RAF1)	XP_005265417.1:n.1418-307G>T
XM_011533974.1:c.1504G>T (RAF1)	XP_011532276.1:p.Val502Phe
XM_011533975.1:c.1261G>T (RAF1)	XP_011532277.1:p.Val421Phe
NM_001354689.1:c.1564G>T (RAF1)	NP_001341618.1:p.Val522Phe
NM_001354690.1:c.1504G>T (RAF1)	NP_001341619.1:p.Val502Phe
NM_001354691.1:c.1261G>T (RAF1)	NP_001341620.1:p.Val421Phe
NM_001354692.1:c.1261G>T (RAF1)	NP_001341621.1:p.Val421Phe
NM_001354693.1:c.1405G>T (RAF1)	NP_001341622.1:p.Val469Phe
NM_001354694.1:c.1321G>T (RAF1)	NP_001341623.1:p.Val441Phe
NM_001354695.1:c.1162G>T (RAF1)	NP_001341624.1:p.Val388Phe
NR_148940.1:n.2032G>T (RAF1)
NR_148941.1:n.1978G>T (RAF1)
NR_148942.1:n.1917G>T (RAF1)
XM_011533974.3:c.1504G>T (RAF1)	XP_011532276.1:p.Val502Phe
XM_017006966.1:c.1405G>T (RAF1)	XP_016862455.1:p.Val469Phe
NM_001354689.3:c.1564G>T (RAF1)	NP_001341618.1:p.Val522Phe
NM_001354690.2:c.1504G>T (RAF1)	NP_001341619.1:p.Val502Phe
NM_001354691.2:c.1261G>T (RAF1)	NP_001341620.1:p.Val421Phe
NM_001354692.2:c.1261G>T (RAF1)	NP_001341621.1:p.Val421Phe
NM_001354693.2:c.1405G>T (RAF1)	NP_001341622.1:p.Val469Phe
NM_001354694.2:c.1321G>T (RAF1)	NP_001341623.1:p.Val441Phe
NM_001354695.2:c.1162G>T (RAF1)	NP_001341624.1:p.Val388Phe
NR_148940.2:n.1948G>T (RAF1)
NR_148941.2:n.1894G>T (RAF1)
NR_148942.2:n.1833G>T (RAF1)
NM_001354690.3:c.1504G>T (RAF1)	NP_001341619.1:p.Val502Phe
NM_001354691.3:c.1261G>T (RAF1)	NP_001341620.1:p.Val421Phe
NM_001354692.3:c.1261G>T (RAF1)	NP_001341621.1:p.Val421Phe
NM_001354693.3:c.1405G>T (RAF1)	NP_001341622.1:p.Val469Phe
NM_001354694.3:c.1321G>T (RAF1)	NP_001341623.1:p.Val441Phe
NM_001354695.3:c.1162G>T (RAF1)	NP_001341624.1:p.Val388Phe
NM_002880.4:c.1504G>T (RAF1) MANE Select	NP_002871.1:p.Val502Phe
NR_148940.3:n.1948G>T (RAF1)
NR_148941.3:n.1894G>T (RAF1)
NR_148942.3:n.1833G>T (RAF1)