Canonical Allele Identifier: CA351496912

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626450A>G (hg19) ; chr3:g.12584951A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584951A>G , CM000665.2:g.12584951A>G	GRCh38
NC_000003.11:g.12626450A>G , CM000665.1:g.12626450A>G	GRCh37
NC_000003.10:g.12601450A>G	NCBI36
NG_007467.1:g.84229T>C , LRG_413:g.84229T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1364T>C (RAF1)	ENSP00000401088.1:n.*1364T>C
ENST00000432427.3:c.1016T>C (RAF1)
ENST00000460610.2:n.6011T>C (RAF1)
ENST00000471449.2:n.509T>C (RAF1)
ENST00000475353.2:n.3979T>C (RAF1)
ENST00000684903.1:c.*1376T>C (RAF1)	ENSP00000508612.1:n.*1376T>C
ENST00000685348.1:c.*1410T>C (RAF1)	ENSP00000510285.1:n.*1410T>C
ENST00000685437.1:c.1600T>C (RAF1)	ENSP00000508794.1:p.Ser534Pro
ENST00000685653.1:c.1699T>C (RAF1)	ENSP00000509968.1:p.Ser567Pro
ENST00000685697.1:n.2434T>C (RAF1)
ENST00000685738.1:c.*663T>C (RAF1)	ENSP00000510156.1:n.*663T>C
ENST00000686409.1:n.5108T>C (RAF1)
ENST00000686455.1:n.4420T>C (RAF1)
ENST00000686762.1:c.*258T>C (RAF1)	ENSP00000509767.1:n.*258T>C
ENST00000687257.1:n.4153T>C (RAF1)
ENST00000687326.1:c.*2991T>C (RAF1)	ENSP00000509665.1:n.*2991T>C
ENST00000687505.1:n.1817T>C (RAF1)
ENST00000687923.1:c.1588T>C (RAF1)	ENSP00000510255.1:p.Ser530Pro
ENST00000688269.1:n.2295T>C (RAF1)
ENST00000688444.1:n.3816T>C (RAF1)
ENST00000688543.1:c.1600T>C (RAF1)	ENSP00000509612.1:p.Ser534Pro
ENST00000688625.1:c.*3068T>C (RAF1)	ENSP00000509522.1:n.*3068T>C
ENST00000688803.1:n.3127T>C (RAF1)
ENST00000688914.1:n.1112T>C (RAF1)
ENST00000689097.1:c.*1376T>C (RAF1)	ENSP00000509756.1:n.*1376T>C
ENST00000689389.1:c.1522T>C (RAF1)	ENSP00000510213.1:p.Ser508Pro
ENST00000689418.1:c.*3594T>C (RAF1)	ENSP00000509467.1:n.*3594T>C
ENST00000689540.1:n.4067T>C (RAF1)
ENST00000689876.1:c.*248T>C (RAF1)	ENSP00000508535.1:n.*248T>C
ENST00000689914.1:c.*633T>C (RAF1)	ENSP00000509847.1:n.*633T>C
ENST00000690397.1:c.1588T>C (RAF1)	ENSP00000508730.1:p.Ser530Pro
ENST00000690460.1:c.1687T>C (RAF1)	ENSP00000509106.1:p.Ser563Pro
ENST00000690585.1:c.425T>C (RAF1)
ENST00000690625.1:n.2735T>C (RAF1)
ENST00000691396.1:c.*1571T>C (RAF1)	ENSP00000510712.1:n.*1571T>C
ENST00000691643.1:n.2752T>C (RAF1)
ENST00000691724.1:c.*656T>C (RAF1)	ENSP00000509255.1:n.*656T>C
ENST00000691779.1:c.*1277T>C (RAF1)	ENSP00000508592.1:n.*1277T>C
ENST00000691888.1:c.573T>C (RAF1)
ENST00000691899.1:c.1699T>C (RAF1)	ENSP00000508763.1:p.Ser567Pro
ENST00000692069.1:n.4623T>C (RAF1)
ENST00000692093.1:c.1600T>C (RAF1)	ENSP00000509669.1:p.Ser534Pro
ENST00000692311.1:n.2523T>C (RAF1)
ENST00000692558.1:n.4282T>C (RAF1)
ENST00000692773.1:c.*1436T>C (RAF1)	ENSP00000509055.1:n.*1436T>C
ENST00000692830.1:c.*1444T>C (RAF1)	ENSP00000509461.1:n.*1444T>C
ENST00000693312.1:c.1474T>C (RAF1)	ENSP00000508686.1:p.Ser492Pro
ENST00000693664.1:c.*150T>C (RAF1)	ENSP00000509614.1:n.*150T>C
ENST00000693705.1:c.*1078T>C (RAF1)	ENSP00000510697.1:n.*1078T>C
ENST00000251849.9:c.1699T>C (RAF1) MANE Select	ENSP00000251849.4:p.Ser567Pro
ENST00000442415.7:c.1759T>C (RAF1)	ENSP00000401888.2:p.Ser587Pro
ENST00000676541.1:c.*2698A>G (MKRN2)	ENSP00000503730.1:n.*2698A>G
ENST00000677142.1:c.*2698A>G (MKRN2)	ENSP00000504455.1:n.*2698A>G
ENST00000677816.1:c.*1253A>G (MKRN2)	ENSP00000502893.1:n.*1253A>G
ENST00000677941.1:n.2761A>G (MKRN2)
ENST00000251849.8:c.1699T>C (RAF1)	ENSP00000251849.4:p.Ser567Pro
ENST00000423275.5:c.*1376T>C (RAF1)	ENSP00000401088.1:n.*1376T>C
ENST00000432427.2:c.1336T>C (RAF1)	ENSP00000398591.2:p.Ser446Pro
ENST00000442415.6:c.1759T>C (RAF1)	ENSP00000401888.2:p.Ser587Pro
ENST00000471449.1:n.388T>C (RAF1)
NM_002880.3:c.1699T>C , LRG_413t1:c.1699T>C (RAF1)	NP_002871.1:p.Ser567Pro
XM_005265355.1:c.1699T>C (RAF1)	XP_005265412.1:p.Ser567Pro
XM_005265357.1:c.1600T>C (RAF1)	XP_005265414.1:p.Ser534Pro
XM_005265358.3:c.1456T>C (RAF1)	XP_005265415.1:p.Ser486Pro
XM_005265359.3:c.1357T>C (RAF1)	XP_005265416.1:p.Ser453Pro
XM_011533974.1:c.1699T>C (RAF1)	XP_011532276.1:p.Ser567Pro
XM_011533975.1:c.1456T>C (RAF1)	XP_011532277.1:p.Ser486Pro
NM_001354689.1:c.1759T>C (RAF1)	NP_001341618.1:p.Ser587Pro
NM_001354690.1:c.1699T>C (RAF1)	NP_001341619.1:p.Ser567Pro
NM_001354691.1:c.1456T>C (RAF1)	NP_001341620.1:p.Ser486Pro
NM_001354692.1:c.1456T>C (RAF1)	NP_001341621.1:p.Ser486Pro
NM_001354693.1:c.1600T>C (RAF1)	NP_001341622.1:p.Ser534Pro
NM_001354694.1:c.1516T>C (RAF1)	NP_001341623.1:p.Ser506Pro
NM_001354695.1:c.1357T>C (RAF1)	NP_001341624.1:p.Ser453Pro
NR_148940.1:n.2227T>C (RAF1)
NR_148941.1:n.2173T>C (RAF1)
NR_148942.1:n.2112T>C (RAF1)
XM_011533974.3:c.1699T>C (RAF1)	XP_011532276.1:p.Ser567Pro
XM_017006966.1:c.1600T>C (RAF1)	XP_016862455.1:p.Ser534Pro
NM_001354689.3:c.1759T>C (RAF1)	NP_001341618.1:p.Ser587Pro
NM_001354690.2:c.1699T>C (RAF1)	NP_001341619.1:p.Ser567Pro
NM_001354691.2:c.1456T>C (RAF1)	NP_001341620.1:p.Ser486Pro
NM_001354692.2:c.1456T>C (RAF1)	NP_001341621.1:p.Ser486Pro
NM_001354693.2:c.1600T>C (RAF1)	NP_001341622.1:p.Ser534Pro
NM_001354694.2:c.1516T>C (RAF1)	NP_001341623.1:p.Ser506Pro
NM_001354695.2:c.1357T>C (RAF1)	NP_001341624.1:p.Ser453Pro
NR_148940.2:n.2143T>C (RAF1)
NR_148941.2:n.2089T>C (RAF1)
NR_148942.2:n.2028T>C (RAF1)
NM_001354690.3:c.1699T>C (RAF1)	NP_001341619.1:p.Ser567Pro
NM_001354691.3:c.1456T>C (RAF1)	NP_001341620.1:p.Ser486Pro
NM_001354692.3:c.1456T>C (RAF1)	NP_001341621.1:p.Ser486Pro
NM_001354693.3:c.1600T>C (RAF1)	NP_001341622.1:p.Ser534Pro
NM_001354694.3:c.1516T>C (RAF1)	NP_001341623.1:p.Ser506Pro
NM_001354695.3:c.1357T>C (RAF1)	NP_001341624.1:p.Ser453Pro
NM_002880.4:c.1699T>C (RAF1) MANE Select	NP_002871.1:p.Ser567Pro
NR_148940.3:n.2143T>C (RAF1)
NR_148941.3:n.2089T>C (RAF1)
NR_148942.3:n.2028T>C (RAF1)