Canonical Allele Identifier: CA351496724

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626410G>A (hg19) ; chr3:g.12584911G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584911G>A , CM000665.2:g.12584911G>A	GRCh38
NC_000003.11:g.12626410G>A , CM000665.1:g.12626410G>A	GRCh37
NC_000003.10:g.12601410G>A	NCBI36
NG_007467.1:g.84269C>T , LRG_413:g.84269C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1404C>T (RAF1)	ENSP00000401088.1:n.*1404C>T
ENST00000432427.3:c.1056C>T (RAF1)
ENST00000460610.2:n.6051C>T (RAF1)
ENST00000471449.2:n.549C>T (RAF1)
ENST00000475353.2:n.4019C>T (RAF1)
ENST00000684903.1:c.*1416C>T (RAF1)	ENSP00000508612.1:n.*1416C>T
ENST00000685348.1:c.*1450C>T (RAF1)	ENSP00000510285.1:n.*1450C>T
ENST00000685437.1:c.1640C>T (RAF1)	ENSP00000508794.1:p.Ala547Val
ENST00000685653.1:c.1739C>T (RAF1)	ENSP00000509968.1:p.Ala580Val
ENST00000685697.1:n.2474C>T (RAF1)
ENST00000685738.1:c.*703C>T (RAF1)	ENSP00000510156.1:n.*703C>T
ENST00000686409.1:n.5148C>T (RAF1)
ENST00000686455.1:n.4460C>T (RAF1)
ENST00000686762.1:c.*298C>T (RAF1)	ENSP00000509767.1:n.*298C>T
ENST00000687257.1:n.4193C>T (RAF1)
ENST00000687326.1:c.*3031C>T (RAF1)	ENSP00000509665.1:n.*3031C>T
ENST00000687505.1:n.1857C>T (RAF1)
ENST00000687923.1:c.1628C>T (RAF1)	ENSP00000510255.1:p.Ala543Val
ENST00000688269.1:n.2335C>T (RAF1)
ENST00000688444.1:n.3856C>T (RAF1)
ENST00000688543.1:c.1640C>T (RAF1)	ENSP00000509612.1:p.Ala547Val
ENST00000688625.1:c.*3108C>T (RAF1)	ENSP00000509522.1:n.*3108C>T
ENST00000688803.1:n.3167C>T (RAF1)
ENST00000688914.1:n.1152C>T (RAF1)
ENST00000689097.1:c.*1416C>T (RAF1)	ENSP00000509756.1:n.*1416C>T
ENST00000689389.1:c.1562C>T (RAF1)	ENSP00000510213.1:p.Ala521Val
ENST00000689418.1:c.*3634C>T (RAF1)	ENSP00000509467.1:n.*3634C>T
ENST00000689540.1:n.4107C>T (RAF1)
ENST00000689876.1:c.*288C>T (RAF1)	ENSP00000508535.1:n.*288C>T
ENST00000689914.1:c.*673C>T (RAF1)	ENSP00000509847.1:n.*673C>T
ENST00000690397.1:c.1628C>T (RAF1)	ENSP00000508730.1:p.Ala543Val
ENST00000690460.1:c.1727C>T (RAF1)	ENSP00000509106.1:p.Ala576Val
ENST00000690585.1:c.465C>T (RAF1)
ENST00000690625.1:n.2775C>T (RAF1)
ENST00000691396.1:c.*1611C>T (RAF1)	ENSP00000510712.1:n.*1611C>T
ENST00000691643.1:n.2792C>T (RAF1)
ENST00000691724.1:c.*696C>T (RAF1)	ENSP00000509255.1:n.*696C>T
ENST00000691779.1:c.*1317C>T (RAF1)	ENSP00000508592.1:n.*1317C>T
ENST00000691888.1:c.613C>T (RAF1)
ENST00000691899.1:c.1739C>T (RAF1)	ENSP00000508763.1:p.Ala580Val
ENST00000692069.1:n.4663C>T (RAF1)
ENST00000692093.1:c.1640C>T (RAF1)	ENSP00000509669.1:p.Ala547Val
ENST00000692311.1:n.2563C>T (RAF1)
ENST00000692558.1:n.4322C>T (RAF1)
ENST00000692773.1:c.*1476C>T (RAF1)	ENSP00000509055.1:n.*1476C>T
ENST00000692830.1:c.*1484C>T (RAF1)	ENSP00000509461.1:n.*1484C>T
ENST00000693312.1:c.1514C>T (RAF1)	ENSP00000508686.1:p.Ala505Val
ENST00000693664.1:c.*190C>T (RAF1)	ENSP00000509614.1:n.*190C>T
ENST00000693705.1:c.*1118C>T (RAF1)	ENSP00000510697.1:n.*1118C>T
ENST00000251849.9:c.1739C>T (RAF1) MANE Select	ENSP00000251849.4:p.Ala580Val
ENST00000442415.7:c.1799C>T (RAF1)	ENSP00000401888.2:p.Ala600Val
ENST00000676541.1:c.*2658G>A (MKRN2)	ENSP00000503730.1:n.*2658G>A
ENST00000677142.1:c.*2658G>A (MKRN2)	ENSP00000504455.1:n.*2658G>A
ENST00000677816.1:c.*1213G>A (MKRN2)	ENSP00000502893.1:n.*1213G>A
ENST00000677941.1:n.2721G>A (MKRN2)
ENST00000251849.8:c.1739C>T (RAF1)	ENSP00000251849.4:p.Ala580Val
ENST00000423275.5:c.*1416C>T (RAF1)	ENSP00000401088.1:n.*1416C>T
ENST00000432427.2:c.1376C>T (RAF1)	ENSP00000398591.2:p.Ala459Val
ENST00000442415.6:c.1799C>T (RAF1)	ENSP00000401888.2:p.Ala600Val
ENST00000471449.1:n.428C>T (RAF1)
NM_002880.3:c.1739C>T , LRG_413t1:c.1739C>T (RAF1)	NP_002871.1:p.Ala580Val
XM_005265355.1:c.1739C>T (RAF1)	XP_005265412.1:p.Ala580Val
XM_005265357.1:c.1640C>T (RAF1)	XP_005265414.1:p.Ala547Val
XM_005265358.3:c.1496C>T (RAF1)	XP_005265415.1:p.Ala499Val
XM_005265359.3:c.1397C>T (RAF1)	XP_005265416.1:p.Ala466Val
XM_011533974.1:c.1739C>T (RAF1)	XP_011532276.1:p.Ala580Val
XM_011533975.1:c.1496C>T (RAF1)	XP_011532277.1:p.Ala499Val
NM_001354689.1:c.1799C>T (RAF1)	NP_001341618.1:p.Ala600Val
NM_001354690.1:c.1739C>T (RAF1)	NP_001341619.1:p.Ala580Val
NM_001354691.1:c.1496C>T (RAF1)	NP_001341620.1:p.Ala499Val
NM_001354692.1:c.1496C>T (RAF1)	NP_001341621.1:p.Ala499Val
NM_001354693.1:c.1640C>T (RAF1)	NP_001341622.1:p.Ala547Val
NM_001354694.1:c.1556C>T (RAF1)	NP_001341623.1:p.Ala519Val
NM_001354695.1:c.1397C>T (RAF1)	NP_001341624.1:p.Ala466Val
NR_148940.1:n.2267C>T (RAF1)
NR_148941.1:n.2213C>T (RAF1)
NR_148942.1:n.2152C>T (RAF1)
XM_011533974.3:c.1739C>T (RAF1)	XP_011532276.1:p.Ala580Val
XM_017006966.1:c.1640C>T (RAF1)	XP_016862455.1:p.Ala547Val
NM_001354689.3:c.1799C>T (RAF1)	NP_001341618.1:p.Ala600Val
NM_001354690.2:c.1739C>T (RAF1)	NP_001341619.1:p.Ala580Val
NM_001354691.2:c.1496C>T (RAF1)	NP_001341620.1:p.Ala499Val
NM_001354692.2:c.1496C>T (RAF1)	NP_001341621.1:p.Ala499Val
NM_001354693.2:c.1640C>T (RAF1)	NP_001341622.1:p.Ala547Val
NM_001354694.2:c.1556C>T (RAF1)	NP_001341623.1:p.Ala519Val
NM_001354695.2:c.1397C>T (RAF1)	NP_001341624.1:p.Ala466Val
NR_148940.2:n.2183C>T (RAF1)
NR_148941.2:n.2129C>T (RAF1)
NR_148942.2:n.2068C>T (RAF1)
NM_001354690.3:c.1739C>T (RAF1)	NP_001341619.1:p.Ala580Val
NM_001354691.3:c.1496C>T (RAF1)	NP_001341620.1:p.Ala499Val
NM_001354692.3:c.1496C>T (RAF1)	NP_001341621.1:p.Ala499Val
NM_001354693.3:c.1640C>T (RAF1)	NP_001341622.1:p.Ala547Val
NM_001354694.3:c.1556C>T (RAF1)	NP_001341623.1:p.Ala519Val
NM_001354695.3:c.1397C>T (RAF1)	NP_001341624.1:p.Ala466Val
NM_002880.4:c.1739C>T (RAF1) MANE Select	NP_002871.1:p.Ala580Val
NR_148940.3:n.2183C>T (RAF1)
NR_148941.3:n.2129C>T (RAF1)
NR_148942.3:n.2068C>T (RAF1)