Canonical Allele Identifier: CA351498761

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12627182T>C (hg19) ; chr3:g.12585683T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585683T>C , CM000665.2:g.12585683T>C	GRCh38
NC_000003.11:g.12627182T>C , CM000665.1:g.12627182T>C	GRCh37
NC_000003.10:g.12602182T>C	NCBI36
NG_007467.1:g.83497A>G , LRG_413:g.83497A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1199A>G (RAF1)	ENSP00000401088.1:n.*1199A>G
ENST00000432427.3:c.851A>G (RAF1)
ENST00000460610.2:n.5279A>G (RAF1)
ENST00000471449.2:n.344A>G (RAF1)
ENST00000475353.2:n.3247A>G (RAF1)
ENST00000684903.1:c.*1211A>G (RAF1)	ENSP00000508612.1:n.*1211A>G
ENST00000685348.1:c.*1095-277A>G (RAF1)	ENSP00000510285.1:n.*1095-277A>G
ENST00000685437.1:c.1435A>G (RAF1)	ENSP00000508794.1:p.Met479Val
ENST00000685653.1:c.1534A>G (RAF1)	ENSP00000509968.1:p.Met512Val
ENST00000685697.1:n.2269A>G (RAF1)
ENST00000685738.1:c.*498A>G (RAF1)	ENSP00000510156.1:n.*498A>G
ENST00000686409.1:n.4376A>G (RAF1)
ENST00000686455.1:n.3688A>G (RAF1)
ENST00000686762.1:c.*93A>G (RAF1)	ENSP00000509767.1:n.*93A>G
ENST00000687257.1:n.3561A>G (RAF1)
ENST00000687326.1:c.*2259A>G (RAF1)	ENSP00000509665.1:n.*2259A>G
ENST00000687505.1:n.1652A>G (RAF1)
ENST00000687923.1:c.1423A>G (RAF1)	ENSP00000510255.1:p.Met475Val
ENST00000688269.1:n.2130A>G (RAF1)
ENST00000688444.1:n.3651A>G (RAF1)
ENST00000688543.1:c.1435A>G (RAF1)	ENSP00000509612.1:p.Met479Val
ENST00000688625.1:c.*2903A>G (RAF1)	ENSP00000509522.1:n.*2903A>G
ENST00000688803.1:n.2965-430A>G (RAF1)
ENST00000688914.1:n.520A>G (RAF1)
ENST00000689097.1:c.*1211A>G (RAF1)	ENSP00000509756.1:n.*1211A>G
ENST00000689389.1:c.1357A>G (RAF1)	ENSP00000510213.1:p.Met453Val
ENST00000689418.1:c.*3002A>G (RAF1)	ENSP00000509467.1:n.*3002A>G
ENST00000689540.1:n.3475A>G (RAF1)
ENST00000689876.1:c.1418-277A>G (RAF1)	ENSP00000508535.1:n.1418-277A>G
ENST00000689914.1:c.*468A>G (RAF1)	ENSP00000509847.1:n.*468A>G
ENST00000690397.1:c.1423A>G (RAF1)	ENSP00000508730.1:p.Met475Val
ENST00000690460.1:c.1522A>G (RAF1)	ENSP00000509106.1:p.Met508Val
ENST00000690585.1:c.263-430A>G (RAF1)
ENST00000690625.1:n.2570A>G (RAF1)
ENST00000691396.1:c.*1406A>G (RAF1)	ENSP00000510712.1:n.*1406A>G
ENST00000691643.1:n.2160A>G (RAF1)
ENST00000691724.1:c.*491A>G (RAF1)	ENSP00000509255.1:n.*491A>G
ENST00000691779.1:c.*1112A>G (RAF1)	ENSP00000508592.1:n.*1112A>G
ENST00000691888.1:c.408A>G (RAF1)
ENST00000691899.1:c.1534A>G (RAF1)	ENSP00000508763.1:p.Met512Val
ENST00000692069.1:n.3891A>G (RAF1)
ENST00000692093.1:c.1435A>G (RAF1)	ENSP00000509669.1:p.Met479Val
ENST00000692311.1:n.2358A>G (RAF1)
ENST00000692558.1:n.3690A>G (RAF1)
ENST00000692773.1:c.*1271A>G (RAF1)	ENSP00000509055.1:n.*1271A>G
ENST00000692830.1:c.*1279A>G (RAF1)	ENSP00000509461.1:n.*1279A>G
ENST00000693312.1:c.1309A>G (RAF1)	ENSP00000508686.1:p.Met437Val
ENST00000693664.1:c.1488-430A>G (RAF1)	ENSP00000509614.1:n.1488-430A>G
ENST00000693705.1:c.*1048-702A>G (RAF1)	ENSP00000510697.1:n.*1048-702A>G
ENST00000251849.9:c.1534A>G (RAF1) MANE Select	ENSP00000251849.4:p.Met512Val
ENST00000442415.7:c.1594A>G (RAF1)	ENSP00000401888.2:p.Met532Val
ENST00000676541.1:c.*3430T>C (MKRN2)	ENSP00000503730.1:n.*3430T>C
ENST00000677142.1:c.*3430T>C (MKRN2)	ENSP00000504455.1:n.*3430T>C
ENST00000677816.1:c.*1985T>C (MKRN2)	ENSP00000502893.1:n.*1985T>C
ENST00000677941.1:n.3493T>C (MKRN2)
ENST00000251849.8:c.1534A>G (RAF1)	ENSP00000251849.4:p.Met512Val
ENST00000423275.5:c.*1211A>G (RAF1)	ENSP00000401088.1:n.*1211A>G
ENST00000432427.2:c.1171A>G (RAF1)	ENSP00000398591.2:p.Met391Val
ENST00000442415.6:c.1594A>G (RAF1)	ENSP00000401888.2:p.Met532Val
ENST00000471449.1:n.223A>G (RAF1)
NM_002880.3:c.1534A>G , LRG_413t1:c.1534A>G (RAF1)	NP_002871.1:p.Met512Val
XM_005265355.1:c.1534A>G (RAF1)	XP_005265412.1:p.Met512Val
XM_005265357.1:c.1435A>G (RAF1)	XP_005265414.1:p.Met479Val
XM_005265358.3:c.1291A>G (RAF1)	XP_005265415.1:p.Met431Val
XM_005265359.3:c.1192A>G (RAF1)	XP_005265416.1:p.Met398Val
XM_005265360.1:c.1418-277A>G (RAF1)	XP_005265417.1:n.1418-277A>G
XM_011533974.1:c.1534A>G (RAF1)	XP_011532276.1:p.Met512Val
XM_011533975.1:c.1291A>G (RAF1)	XP_011532277.1:p.Met431Val
NM_001354689.1:c.1594A>G (RAF1)	NP_001341618.1:p.Met532Val
NM_001354690.1:c.1534A>G (RAF1)	NP_001341619.1:p.Met512Val
NM_001354691.1:c.1291A>G (RAF1)	NP_001341620.1:p.Met431Val
NM_001354692.1:c.1291A>G (RAF1)	NP_001341621.1:p.Met431Val
NM_001354693.1:c.1435A>G (RAF1)	NP_001341622.1:p.Met479Val
NM_001354694.1:c.1351A>G (RAF1)	NP_001341623.1:p.Met451Val
NM_001354695.1:c.1192A>G (RAF1)	NP_001341624.1:p.Met398Val
NR_148940.1:n.2062A>G (RAF1)
NR_148941.1:n.2008A>G (RAF1)
NR_148942.1:n.1947A>G (RAF1)
XM_011533974.3:c.1534A>G (RAF1)	XP_011532276.1:p.Met512Val
XM_017006966.1:c.1435A>G (RAF1)	XP_016862455.1:p.Met479Val
NM_001354689.3:c.1594A>G (RAF1)	NP_001341618.1:p.Met532Val
NM_001354690.2:c.1534A>G (RAF1)	NP_001341619.1:p.Met512Val
NM_001354691.2:c.1291A>G (RAF1)	NP_001341620.1:p.Met431Val
NM_001354692.2:c.1291A>G (RAF1)	NP_001341621.1:p.Met431Val
NM_001354693.2:c.1435A>G (RAF1)	NP_001341622.1:p.Met479Val
NM_001354694.2:c.1351A>G (RAF1)	NP_001341623.1:p.Met451Val
NM_001354695.2:c.1192A>G (RAF1)	NP_001341624.1:p.Met398Val
NR_148940.2:n.1978A>G (RAF1)
NR_148941.2:n.1924A>G (RAF1)
NR_148942.2:n.1863A>G (RAF1)
NM_001354690.3:c.1534A>G (RAF1)	NP_001341619.1:p.Met512Val
NM_001354691.3:c.1291A>G (RAF1)	NP_001341620.1:p.Met431Val
NM_001354692.3:c.1291A>G (RAF1)	NP_001341621.1:p.Met431Val
NM_001354693.3:c.1435A>G (RAF1)	NP_001341622.1:p.Met479Val
NM_001354694.3:c.1351A>G (RAF1)	NP_001341623.1:p.Met451Val
NM_001354695.3:c.1192A>G (RAF1)	NP_001341624.1:p.Met398Val
NM_002880.4:c.1534A>G (RAF1) MANE Select	NP_002871.1:p.Met512Val
NR_148940.3:n.1978A>G (RAF1)
NR_148941.3:n.1924A>G (RAF1)
NR_148942.3:n.1863A>G (RAF1)