Canonical Allele Identifier: CA351497072

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626475G>C (hg19) ; chr3:g.12584976G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584976G>C , CM000665.2:g.12584976G>C	GRCh38
NC_000003.11:g.12626475G>C , CM000665.1:g.12626475G>C	GRCh37
NC_000003.10:g.12601475G>C	NCBI36
NG_007467.1:g.84204C>G , LRG_413:g.84204C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1339C>G (RAF1)	ENSP00000401088.1:n.*1339C>G
ENST00000432427.3:c.991C>G (RAF1)
ENST00000460610.2:n.5986C>G (RAF1)
ENST00000471449.2:n.484C>G (RAF1)
ENST00000475353.2:n.3954C>G (RAF1)
ENST00000684903.1:c.*1351C>G (RAF1)	ENSP00000508612.1:n.*1351C>G
ENST00000685348.1:c.*1385C>G (RAF1)	ENSP00000510285.1:n.*1385C>G
ENST00000685437.1:c.1575C>G (RAF1)	ENSP00000508794.1:p.Ile525Met
ENST00000685653.1:c.1674C>G (RAF1)	ENSP00000509968.1:p.Ile558Met
ENST00000685697.1:n.2409C>G (RAF1)
ENST00000685738.1:c.*638C>G (RAF1)	ENSP00000510156.1:n.*638C>G
ENST00000686409.1:n.5083C>G (RAF1)
ENST00000686455.1:n.4395C>G (RAF1)
ENST00000686762.1:c.*233C>G (RAF1)	ENSP00000509767.1:n.*233C>G
ENST00000687257.1:n.4128C>G (RAF1)
ENST00000687326.1:c.*2966C>G (RAF1)	ENSP00000509665.1:n.*2966C>G
ENST00000687505.1:n.1792C>G (RAF1)
ENST00000687923.1:c.1563C>G (RAF1)	ENSP00000510255.1:p.Ile521Met
ENST00000688269.1:n.2270C>G (RAF1)
ENST00000688444.1:n.3791C>G (RAF1)
ENST00000688543.1:c.1575C>G (RAF1)	ENSP00000509612.1:p.Ile525Met
ENST00000688625.1:c.*3043C>G (RAF1)	ENSP00000509522.1:n.*3043C>G
ENST00000688803.1:n.3102C>G (RAF1)
ENST00000688914.1:n.1087C>G (RAF1)
ENST00000689097.1:c.*1351C>G (RAF1)	ENSP00000509756.1:n.*1351C>G
ENST00000689389.1:c.1497C>G (RAF1)	ENSP00000510213.1:p.Ile499Met
ENST00000689418.1:c.*3569C>G (RAF1)	ENSP00000509467.1:n.*3569C>G
ENST00000689540.1:n.4042C>G (RAF1)
ENST00000689876.1:c.*223C>G (RAF1)	ENSP00000508535.1:n.*223C>G
ENST00000689914.1:c.*608C>G (RAF1)	ENSP00000509847.1:n.*608C>G
ENST00000690397.1:c.1563C>G (RAF1)	ENSP00000508730.1:p.Ile521Met
ENST00000690460.1:c.1662C>G (RAF1)	ENSP00000509106.1:p.Ile554Met
ENST00000690585.1:c.400C>G (RAF1)
ENST00000690625.1:n.2710C>G (RAF1)
ENST00000691396.1:c.*1546C>G (RAF1)	ENSP00000510712.1:n.*1546C>G
ENST00000691643.1:n.2727C>G (RAF1)
ENST00000691724.1:c.*631C>G (RAF1)	ENSP00000509255.1:n.*631C>G
ENST00000691779.1:c.*1252C>G (RAF1)	ENSP00000508592.1:n.*1252C>G
ENST00000691888.1:c.548C>G (RAF1)
ENST00000691899.1:c.1674C>G (RAF1)	ENSP00000508763.1:p.Ile558Met
ENST00000692069.1:n.4598C>G (RAF1)
ENST00000692093.1:c.1575C>G (RAF1)	ENSP00000509669.1:p.Ile525Met
ENST00000692311.1:n.2498C>G (RAF1)
ENST00000692558.1:n.4257C>G (RAF1)
ENST00000692773.1:c.*1411C>G (RAF1)	ENSP00000509055.1:n.*1411C>G
ENST00000692830.1:c.*1419C>G (RAF1)	ENSP00000509461.1:n.*1419C>G
ENST00000693312.1:c.1449C>G (RAF1)	ENSP00000508686.1:p.Ile483Met
ENST00000693664.1:c.*125C>G (RAF1)	ENSP00000509614.1:n.*125C>G
ENST00000693705.1:c.*1053C>G (RAF1)	ENSP00000510697.1:n.*1053C>G
ENST00000251849.9:c.1674C>G (RAF1) MANE Select	ENSP00000251849.4:p.Ile558Met
ENST00000442415.7:c.1734C>G (RAF1)	ENSP00000401888.2:p.Ile578Met
ENST00000676541.1:c.*2723G>C (MKRN2)	ENSP00000503730.1:n.*2723G>C
ENST00000677142.1:c.*2723G>C (MKRN2)	ENSP00000504455.1:n.*2723G>C
ENST00000677816.1:c.*1278G>C (MKRN2)	ENSP00000502893.1:n.*1278G>C
ENST00000677941.1:n.2786G>C (MKRN2)
ENST00000251849.8:c.1674C>G (RAF1)	ENSP00000251849.4:p.Ile558Met
ENST00000423275.5:c.*1351C>G (RAF1)	ENSP00000401088.1:n.*1351C>G
ENST00000432427.2:c.1311C>G (RAF1)	ENSP00000398591.2:p.Ile437Met
ENST00000442415.6:c.1734C>G (RAF1)	ENSP00000401888.2:p.Ile578Met
ENST00000471449.1:n.363C>G (RAF1)
NM_002880.3:c.1674C>G , LRG_413t1:c.1674C>G (RAF1)	NP_002871.1:p.Ile558Met
XM_005265355.1:c.1674C>G (RAF1)	XP_005265412.1:p.Ile558Met
XM_005265357.1:c.1575C>G (RAF1)	XP_005265414.1:p.Ile525Met
XM_005265358.3:c.1431C>G (RAF1)	XP_005265415.1:p.Ile477Met
XM_005265359.3:c.1332C>G (RAF1)	XP_005265416.1:p.Ile444Met
XM_011533974.1:c.1674C>G (RAF1)	XP_011532276.1:p.Ile558Met
XM_011533975.1:c.1431C>G (RAF1)	XP_011532277.1:p.Ile477Met
NM_001354689.1:c.1734C>G (RAF1)	NP_001341618.1:p.Ile578Met
NM_001354690.1:c.1674C>G (RAF1)	NP_001341619.1:p.Ile558Met
NM_001354691.1:c.1431C>G (RAF1)	NP_001341620.1:p.Ile477Met
NM_001354692.1:c.1431C>G (RAF1)	NP_001341621.1:p.Ile477Met
NM_001354693.1:c.1575C>G (RAF1)	NP_001341622.1:p.Ile525Met
NM_001354694.1:c.1491C>G (RAF1)	NP_001341623.1:p.Ile497Met
NM_001354695.1:c.1332C>G (RAF1)	NP_001341624.1:p.Ile444Met
NR_148940.1:n.2202C>G (RAF1)
NR_148941.1:n.2148C>G (RAF1)
NR_148942.1:n.2087C>G (RAF1)
XM_011533974.3:c.1674C>G (RAF1)	XP_011532276.1:p.Ile558Met
XM_017006966.1:c.1575C>G (RAF1)	XP_016862455.1:p.Ile525Met
NM_001354689.3:c.1734C>G (RAF1)	NP_001341618.1:p.Ile578Met
NM_001354690.2:c.1674C>G (RAF1)	NP_001341619.1:p.Ile558Met
NM_001354691.2:c.1431C>G (RAF1)	NP_001341620.1:p.Ile477Met
NM_001354692.2:c.1431C>G (RAF1)	NP_001341621.1:p.Ile477Met
NM_001354693.2:c.1575C>G (RAF1)	NP_001341622.1:p.Ile525Met
NM_001354694.2:c.1491C>G (RAF1)	NP_001341623.1:p.Ile497Met
NM_001354695.2:c.1332C>G (RAF1)	NP_001341624.1:p.Ile444Met
NR_148940.2:n.2118C>G (RAF1)
NR_148941.2:n.2064C>G (RAF1)
NR_148942.2:n.2003C>G (RAF1)
NM_001354690.3:c.1674C>G (RAF1)	NP_001341619.1:p.Ile558Met
NM_001354691.3:c.1431C>G (RAF1)	NP_001341620.1:p.Ile477Met
NM_001354692.3:c.1431C>G (RAF1)	NP_001341621.1:p.Ile477Met
NM_001354693.3:c.1575C>G (RAF1)	NP_001341622.1:p.Ile525Met
NM_001354694.3:c.1491C>G (RAF1)	NP_001341623.1:p.Ile497Met
NM_001354695.3:c.1332C>G (RAF1)	NP_001341624.1:p.Ile444Met
NM_002880.4:c.1674C>G (RAF1) MANE Select	NP_002871.1:p.Ile558Met
NR_148940.3:n.2118C>G (RAF1)
NR_148941.3:n.2064C>G (RAF1)
NR_148942.3:n.2003C>G (RAF1)