Canonical Allele Identifier: CA432272825

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12627207T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585708T>C , CM000665.2:g.12585708T>C	GRCh38
NC_000003.11:g.12627207T>C , CM000665.1:g.12627207T>C	GRCh37
NC_000003.10:g.12602207T>C	NCBI36
NG_007467.1:g.83472A>G , LRG_413:g.83472A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1174A>G (RAF1)	ENSP00000401088.1:n.*1174A>G
ENST00000432427.3:c.826A>G (RAF1)
ENST00000460610.2:n.5254A>G (RAF1)
ENST00000471449.2:n.319A>G (RAF1)
ENST00000475353.2:n.3222A>G (RAF1)
ENST00000684903.1:c.*1186A>G (RAF1)	ENSP00000508612.1:n.*1186A>G
ENST00000685348.1:c.*1095-302A>G (RAF1)	ENSP00000510285.1:n.*1095-302A>G
ENST00000685437.1:c.1410A>G (RAF1)	ENSP00000508794.1:p.Glu470=
ENST00000685653.1:c.1509A>G (RAF1)	ENSP00000509968.1:p.Glu503=
ENST00000685697.1:n.2244A>G (RAF1)
ENST00000685738.1:c.*473A>G (RAF1)	ENSP00000510156.1:n.*473A>G
ENST00000686409.1:n.4351A>G (RAF1)
ENST00000686455.1:n.3663A>G (RAF1)
ENST00000686762.1:c.*68A>G (RAF1)	ENSP00000509767.1:n.*68A>G
ENST00000687257.1:n.3536A>G (RAF1)
ENST00000687326.1:c.*2234A>G (RAF1)	ENSP00000509665.1:n.*2234A>G
ENST00000687505.1:n.1627A>G (RAF1)
ENST00000687923.1:c.1398A>G (RAF1)	ENSP00000510255.1:p.Glu466=
ENST00000688269.1:n.2105A>G (RAF1)
ENST00000688444.1:n.3626A>G (RAF1)
ENST00000688543.1:c.1410A>G (RAF1)	ENSP00000509612.1:p.Glu470=
ENST00000688625.1:c.*2878A>G (RAF1)	ENSP00000509522.1:n.*2878A>G
ENST00000688803.1:n.2965-455A>G (RAF1)
ENST00000688914.1:n.495A>G (RAF1)
ENST00000689097.1:c.*1186A>G (RAF1)	ENSP00000509756.1:n.*1186A>G
ENST00000689389.1:c.1332A>G (RAF1)	ENSP00000510213.1:p.Glu444=
ENST00000689418.1:c.*2977A>G (RAF1)	ENSP00000509467.1:n.*2977A>G
ENST00000689540.1:n.3450A>G (RAF1)
ENST00000689876.1:c.1418-302A>G (RAF1)	ENSP00000508535.1:n.1418-302A>G
ENST00000689914.1:c.*443A>G (RAF1)	ENSP00000509847.1:n.*443A>G
ENST00000690397.1:c.1398A>G (RAF1)	ENSP00000508730.1:p.Glu466=
ENST00000690460.1:c.1497A>G (RAF1)	ENSP00000509106.1:p.Glu499=
ENST00000690585.1:c.263-455A>G (RAF1)
ENST00000690625.1:n.2545A>G (RAF1)
ENST00000691396.1:c.*1381A>G (RAF1)	ENSP00000510712.1:n.*1381A>G
ENST00000691643.1:n.2135A>G (RAF1)
ENST00000691724.1:c.*466A>G (RAF1)	ENSP00000509255.1:n.*466A>G
ENST00000691779.1:c.*1087A>G (RAF1)	ENSP00000508592.1:n.*1087A>G
ENST00000691888.1:c.383A>G (RAF1)
ENST00000691899.1:c.1509A>G (RAF1)	ENSP00000508763.1:p.Glu503=
ENST00000692069.1:n.3866A>G (RAF1)
ENST00000692093.1:c.1410A>G (RAF1)	ENSP00000509669.1:p.Glu470=
ENST00000692311.1:n.2333A>G (RAF1)
ENST00000692558.1:n.3665A>G (RAF1)
ENST00000692773.1:c.*1246A>G (RAF1)	ENSP00000509055.1:n.*1246A>G
ENST00000692830.1:c.*1254A>G (RAF1)	ENSP00000509461.1:n.*1254A>G
ENST00000693312.1:c.1284A>G (RAF1)	ENSP00000508686.1:p.Glu428=
ENST00000693664.1:c.1488-455A>G (RAF1)	ENSP00000509614.1:n.1488-455A>G
ENST00000693705.1:c.*1048-727A>G (RAF1)	ENSP00000510697.1:n.*1048-727A>G
ENST00000251849.9:c.1509A>G (RAF1) MANE Select	ENSP00000251849.4:p.Glu503=
ENST00000442415.7:c.1569A>G (RAF1)	ENSP00000401888.2:p.Glu523=
ENST00000676541.1:c.*3455T>C (MKRN2)	ENSP00000503730.1:n.*3455T>C
ENST00000677142.1:c.*3455T>C (MKRN2)	ENSP00000504455.1:n.*3455T>C
ENST00000677816.1:c.*2010T>C (MKRN2)	ENSP00000502893.1:n.*2010T>C
ENST00000677941.1:n.3518T>C (MKRN2)
ENST00000251849.8:c.1509A>G (RAF1)	ENSP00000251849.4:p.Glu503=
ENST00000423275.5:c.*1186A>G (RAF1)	ENSP00000401088.1:n.*1186A>G
ENST00000432427.2:c.1146A>G (RAF1)	ENSP00000398591.2:p.Glu382=
ENST00000442415.6:c.1569A>G (RAF1)	ENSP00000401888.2:p.Glu523=
ENST00000471449.1:n.198A>G (RAF1)
NM_002880.3:c.1509A>G , LRG_413t1:c.1509A>G (RAF1)	NP_002871.1:p.Glu503=
XM_005265355.1:c.1509A>G (RAF1)	XP_005265412.1:p.Glu503=
XM_005265357.1:c.1410A>G (RAF1)	XP_005265414.1:p.Glu470=
XM_005265358.3:c.1266A>G (RAF1)	XP_005265415.1:p.Glu422=
XM_005265359.3:c.1167A>G (RAF1)	XP_005265416.1:p.Glu389=
XM_005265360.1:c.1418-302A>G (RAF1)	XP_005265417.1:n.1418-302A>G
XM_011533974.1:c.1509A>G (RAF1)	XP_011532276.1:p.Glu503=
XM_011533975.1:c.1266A>G (RAF1)	XP_011532277.1:p.Glu422=
NM_001354689.1:c.1569A>G (RAF1)	NP_001341618.1:p.Glu523=
NM_001354690.1:c.1509A>G (RAF1)	NP_001341619.1:p.Glu503=
NM_001354691.1:c.1266A>G (RAF1)	NP_001341620.1:p.Glu422=
NM_001354692.1:c.1266A>G (RAF1)	NP_001341621.1:p.Glu422=
NM_001354693.1:c.1410A>G (RAF1)	NP_001341622.1:p.Glu470=
NM_001354694.1:c.1326A>G (RAF1)	NP_001341623.1:p.Glu442=
NM_001354695.1:c.1167A>G (RAF1)	NP_001341624.1:p.Glu389=
NR_148940.1:n.2037A>G (RAF1)
NR_148941.1:n.1983A>G (RAF1)
NR_148942.1:n.1922A>G (RAF1)
XM_011533974.3:c.1509A>G (RAF1)	XP_011532276.1:p.Glu503=
XM_017006966.1:c.1410A>G (RAF1)	XP_016862455.1:p.Glu470=
NM_001354689.3:c.1569A>G (RAF1)	NP_001341618.1:p.Glu523=
NM_001354690.2:c.1509A>G (RAF1)	NP_001341619.1:p.Glu503=
NM_001354691.2:c.1266A>G (RAF1)	NP_001341620.1:p.Glu422=
NM_001354692.2:c.1266A>G (RAF1)	NP_001341621.1:p.Glu422=
NM_001354693.2:c.1410A>G (RAF1)	NP_001341622.1:p.Glu470=
NM_001354694.2:c.1326A>G (RAF1)	NP_001341623.1:p.Glu442=
NM_001354695.2:c.1167A>G (RAF1)	NP_001341624.1:p.Glu389=
NR_148940.2:n.1953A>G (RAF1)
NR_148941.2:n.1899A>G (RAF1)
NR_148942.2:n.1838A>G (RAF1)
NM_001354690.3:c.1509A>G (RAF1)	NP_001341619.1:p.Glu503=
NM_001354691.3:c.1266A>G (RAF1)	NP_001341620.1:p.Glu422=
NM_001354692.3:c.1266A>G (RAF1)	NP_001341621.1:p.Glu422=
NM_001354693.3:c.1410A>G (RAF1)	NP_001341622.1:p.Glu470=
NM_001354694.3:c.1326A>G (RAF1)	NP_001341623.1:p.Glu442=
NM_001354695.3:c.1167A>G (RAF1)	NP_001341624.1:p.Glu389=
NM_002880.4:c.1509A>G (RAF1) MANE Select	NP_002871.1:p.Glu503=
NR_148940.3:n.1953A>G (RAF1)
NR_148941.3:n.1899A>G (RAF1)
NR_148942.3:n.1838A>G (RAF1)