Canonical Allele Identifier: CA351498810

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12627190A>C (hg19) ; chr3:g.12585691A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585691A>C , CM000665.2:g.12585691A>C	GRCh38
NC_000003.11:g.12627190A>C , CM000665.1:g.12627190A>C	GRCh37
NC_000003.10:g.12602190A>C	NCBI36
NG_007467.1:g.83489T>G , LRG_413:g.83489T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1191T>G (RAF1)	ENSP00000401088.1:n.*1191T>G
ENST00000432427.3:c.843T>G (RAF1)
ENST00000460610.2:n.5271T>G (RAF1)
ENST00000471449.2:n.336T>G (RAF1)
ENST00000475353.2:n.3239T>G (RAF1)
ENST00000684903.1:c.*1203T>G (RAF1)	ENSP00000508612.1:n.*1203T>G
ENST00000685348.1:c.*1095-285T>G (RAF1)	ENSP00000510285.1:n.*1095-285T>G
ENST00000685437.1:c.1427T>G (RAF1)	ENSP00000508794.1:p.Val476Gly
ENST00000685653.1:c.1526T>G (RAF1)	ENSP00000509968.1:p.Val509Gly
ENST00000685697.1:n.2261T>G (RAF1)
ENST00000685738.1:c.*490T>G (RAF1)	ENSP00000510156.1:n.*490T>G
ENST00000686409.1:n.4368T>G (RAF1)
ENST00000686455.1:n.3680T>G (RAF1)
ENST00000686762.1:c.*85T>G (RAF1)	ENSP00000509767.1:n.*85T>G
ENST00000687257.1:n.3553T>G (RAF1)
ENST00000687326.1:c.*2251T>G (RAF1)	ENSP00000509665.1:n.*2251T>G
ENST00000687505.1:n.1644T>G (RAF1)
ENST00000687923.1:c.1415T>G (RAF1)	ENSP00000510255.1:p.Val472Gly
ENST00000688269.1:n.2122T>G (RAF1)
ENST00000688444.1:n.3643T>G (RAF1)
ENST00000688543.1:c.1427T>G (RAF1)	ENSP00000509612.1:p.Val476Gly
ENST00000688625.1:c.*2895T>G (RAF1)	ENSP00000509522.1:n.*2895T>G
ENST00000688803.1:n.2965-438T>G (RAF1)
ENST00000688914.1:n.512T>G (RAF1)
ENST00000689097.1:c.*1203T>G (RAF1)	ENSP00000509756.1:n.*1203T>G
ENST00000689389.1:c.1349T>G (RAF1)	ENSP00000510213.1:p.Val450Gly
ENST00000689418.1:c.*2994T>G (RAF1)	ENSP00000509467.1:n.*2994T>G
ENST00000689540.1:n.3467T>G (RAF1)
ENST00000689876.1:c.1418-285T>G (RAF1)	ENSP00000508535.1:n.1418-285T>G
ENST00000689914.1:c.*460T>G (RAF1)	ENSP00000509847.1:n.*460T>G
ENST00000690397.1:c.1415T>G (RAF1)	ENSP00000508730.1:p.Val472Gly
ENST00000690460.1:c.1514T>G (RAF1)	ENSP00000509106.1:p.Val505Gly
ENST00000690585.1:c.263-438T>G (RAF1)
ENST00000690625.1:n.2562T>G (RAF1)
ENST00000691396.1:c.*1398T>G (RAF1)	ENSP00000510712.1:n.*1398T>G
ENST00000691643.1:n.2152T>G (RAF1)
ENST00000691724.1:c.*483T>G (RAF1)	ENSP00000509255.1:n.*483T>G
ENST00000691779.1:c.*1104T>G (RAF1)	ENSP00000508592.1:n.*1104T>G
ENST00000691888.1:c.400T>G (RAF1)
ENST00000691899.1:c.1526T>G (RAF1)	ENSP00000508763.1:p.Val509Gly
ENST00000692069.1:n.3883T>G (RAF1)
ENST00000692093.1:c.1427T>G (RAF1)	ENSP00000509669.1:p.Val476Gly
ENST00000692311.1:n.2350T>G (RAF1)
ENST00000692558.1:n.3682T>G (RAF1)
ENST00000692773.1:c.*1263T>G (RAF1)	ENSP00000509055.1:n.*1263T>G
ENST00000692830.1:c.*1271T>G (RAF1)	ENSP00000509461.1:n.*1271T>G
ENST00000693312.1:c.1301T>G (RAF1)	ENSP00000508686.1:p.Val434Gly
ENST00000693664.1:c.1488-438T>G (RAF1)	ENSP00000509614.1:n.1488-438T>G
ENST00000693705.1:c.*1048-710T>G (RAF1)	ENSP00000510697.1:n.*1048-710T>G
ENST00000251849.9:c.1526T>G (RAF1) MANE Select	ENSP00000251849.4:p.Val509Gly
ENST00000442415.7:c.1586T>G (RAF1)	ENSP00000401888.2:p.Val529Gly
ENST00000676541.1:c.*3438A>C (MKRN2)	ENSP00000503730.1:n.*3438A>C
ENST00000677142.1:c.*3438A>C (MKRN2)	ENSP00000504455.1:n.*3438A>C
ENST00000677816.1:c.*1993A>C (MKRN2)	ENSP00000502893.1:n.*1993A>C
ENST00000677941.1:n.3501A>C (MKRN2)
ENST00000251849.8:c.1526T>G (RAF1)	ENSP00000251849.4:p.Val509Gly
ENST00000423275.5:c.*1203T>G (RAF1)	ENSP00000401088.1:n.*1203T>G
ENST00000432427.2:c.1163T>G (RAF1)	ENSP00000398591.2:p.Val388Gly
ENST00000442415.6:c.1586T>G (RAF1)	ENSP00000401888.2:p.Val529Gly
ENST00000471449.1:n.215T>G (RAF1)
NM_002880.3:c.1526T>G , LRG_413t1:c.1526T>G (RAF1)	NP_002871.1:p.Val509Gly
XM_005265355.1:c.1526T>G (RAF1)	XP_005265412.1:p.Val509Gly
XM_005265357.1:c.1427T>G (RAF1)	XP_005265414.1:p.Val476Gly
XM_005265358.3:c.1283T>G (RAF1)	XP_005265415.1:p.Val428Gly
XM_005265359.3:c.1184T>G (RAF1)	XP_005265416.1:p.Val395Gly
XM_005265360.1:c.1418-285T>G (RAF1)	XP_005265417.1:n.1418-285T>G
XM_011533974.1:c.1526T>G (RAF1)	XP_011532276.1:p.Val509Gly
XM_011533975.1:c.1283T>G (RAF1)	XP_011532277.1:p.Val428Gly
NM_001354689.1:c.1586T>G (RAF1)	NP_001341618.1:p.Val529Gly
NM_001354690.1:c.1526T>G (RAF1)	NP_001341619.1:p.Val509Gly
NM_001354691.1:c.1283T>G (RAF1)	NP_001341620.1:p.Val428Gly
NM_001354692.1:c.1283T>G (RAF1)	NP_001341621.1:p.Val428Gly
NM_001354693.1:c.1427T>G (RAF1)	NP_001341622.1:p.Val476Gly
NM_001354694.1:c.1343T>G (RAF1)	NP_001341623.1:p.Val448Gly
NM_001354695.1:c.1184T>G (RAF1)	NP_001341624.1:p.Val395Gly
NR_148940.1:n.2054T>G (RAF1)
NR_148941.1:n.2000T>G (RAF1)
NR_148942.1:n.1939T>G (RAF1)
XM_011533974.3:c.1526T>G (RAF1)	XP_011532276.1:p.Val509Gly
XM_017006966.1:c.1427T>G (RAF1)	XP_016862455.1:p.Val476Gly
NM_001354689.3:c.1586T>G (RAF1)	NP_001341618.1:p.Val529Gly
NM_001354690.2:c.1526T>G (RAF1)	NP_001341619.1:p.Val509Gly
NM_001354691.2:c.1283T>G (RAF1)	NP_001341620.1:p.Val428Gly
NM_001354692.2:c.1283T>G (RAF1)	NP_001341621.1:p.Val428Gly
NM_001354693.2:c.1427T>G (RAF1)	NP_001341622.1:p.Val476Gly
NM_001354694.2:c.1343T>G (RAF1)	NP_001341623.1:p.Val448Gly
NM_001354695.2:c.1184T>G (RAF1)	NP_001341624.1:p.Val395Gly
NR_148940.2:n.1970T>G (RAF1)
NR_148941.2:n.1916T>G (RAF1)
NR_148942.2:n.1855T>G (RAF1)
NM_001354690.3:c.1526T>G (RAF1)	NP_001341619.1:p.Val509Gly
NM_001354691.3:c.1283T>G (RAF1)	NP_001341620.1:p.Val428Gly
NM_001354692.3:c.1283T>G (RAF1)	NP_001341621.1:p.Val428Gly
NM_001354693.3:c.1427T>G (RAF1)	NP_001341622.1:p.Val476Gly
NM_001354694.3:c.1343T>G (RAF1)	NP_001341623.1:p.Val448Gly
NM_001354695.3:c.1184T>G (RAF1)	NP_001341624.1:p.Val395Gly
NM_002880.4:c.1526T>G (RAF1) MANE Select	NP_002871.1:p.Val509Gly
NR_148940.3:n.1970T>G (RAF1)
NR_148941.3:n.1916T>G (RAF1)
NR_148942.3:n.1855T>G (RAF1)