Canonical Allele Identifier: CA432522053

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626451G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584952G>C , CM000665.2:g.12584952G>C	GRCh38
NC_000003.11:g.12626451G>C , CM000665.1:g.12626451G>C	GRCh37
NC_000003.10:g.12601451G>C	NCBI36
NG_007467.1:g.84228C>G , LRG_413:g.84228C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1363C>G (RAF1)	ENSP00000401088.1:n.*1363C>G
ENST00000432427.3:c.1015C>G (RAF1)
ENST00000460610.2:n.6010C>G (RAF1)
ENST00000471449.2:n.508C>G (RAF1)
ENST00000475353.2:n.3978C>G (RAF1)
ENST00000684903.1:c.*1375C>G (RAF1)	ENSP00000508612.1:n.*1375C>G
ENST00000685348.1:c.*1409C>G (RAF1)	ENSP00000510285.1:n.*1409C>G
ENST00000685437.1:c.1599C>G (RAF1)	ENSP00000508794.1:p.Ala533=
ENST00000685653.1:c.1698C>G (RAF1)	ENSP00000509968.1:p.Ala566=
ENST00000685697.1:n.2433C>G (RAF1)
ENST00000685738.1:c.*662C>G (RAF1)	ENSP00000510156.1:n.*662C>G
ENST00000686409.1:n.5107C>G (RAF1)
ENST00000686455.1:n.4419C>G (RAF1)
ENST00000686762.1:c.*257C>G (RAF1)	ENSP00000509767.1:n.*257C>G
ENST00000687257.1:n.4152C>G (RAF1)
ENST00000687326.1:c.*2990C>G (RAF1)	ENSP00000509665.1:n.*2990C>G
ENST00000687505.1:n.1816C>G (RAF1)
ENST00000687923.1:c.1587C>G (RAF1)	ENSP00000510255.1:p.Ala529=
ENST00000688269.1:n.2294C>G (RAF1)
ENST00000688444.1:n.3815C>G (RAF1)
ENST00000688543.1:c.1599C>G (RAF1)	ENSP00000509612.1:p.Ala533=
ENST00000688625.1:c.*3067C>G (RAF1)	ENSP00000509522.1:n.*3067C>G
ENST00000688803.1:n.3126C>G (RAF1)
ENST00000688914.1:n.1111C>G (RAF1)
ENST00000689097.1:c.*1375C>G (RAF1)	ENSP00000509756.1:n.*1375C>G
ENST00000689389.1:c.1521C>G (RAF1)	ENSP00000510213.1:p.Ala507=
ENST00000689418.1:c.*3593C>G (RAF1)	ENSP00000509467.1:n.*3593C>G
ENST00000689540.1:n.4066C>G (RAF1)
ENST00000689876.1:c.*247C>G (RAF1)	ENSP00000508535.1:n.*247C>G
ENST00000689914.1:c.*632C>G (RAF1)	ENSP00000509847.1:n.*632C>G
ENST00000690397.1:c.1587C>G (RAF1)	ENSP00000508730.1:p.Ala529=
ENST00000690460.1:c.1686C>G (RAF1)	ENSP00000509106.1:p.Ala562=
ENST00000690585.1:c.424C>G (RAF1)
ENST00000690625.1:n.2734C>G (RAF1)
ENST00000691396.1:c.*1570C>G (RAF1)	ENSP00000510712.1:n.*1570C>G
ENST00000691643.1:n.2751C>G (RAF1)
ENST00000691724.1:c.*655C>G (RAF1)	ENSP00000509255.1:n.*655C>G
ENST00000691779.1:c.*1276C>G (RAF1)	ENSP00000508592.1:n.*1276C>G
ENST00000691888.1:c.572C>G (RAF1)
ENST00000691899.1:c.1698C>G (RAF1)	ENSP00000508763.1:p.Ala566=
ENST00000692069.1:n.4622C>G (RAF1)
ENST00000692093.1:c.1599C>G (RAF1)	ENSP00000509669.1:p.Ala533=
ENST00000692311.1:n.2522C>G (RAF1)
ENST00000692558.1:n.4281C>G (RAF1)
ENST00000692773.1:c.*1435C>G (RAF1)	ENSP00000509055.1:n.*1435C>G
ENST00000692830.1:c.*1443C>G (RAF1)	ENSP00000509461.1:n.*1443C>G
ENST00000693312.1:c.1473C>G (RAF1)	ENSP00000508686.1:p.Ala491=
ENST00000693664.1:c.*149C>G (RAF1)	ENSP00000509614.1:n.*149C>G
ENST00000693705.1:c.*1077C>G (RAF1)	ENSP00000510697.1:n.*1077C>G
ENST00000251849.9:c.1698C>G (RAF1) MANE Select	ENSP00000251849.4:p.Ala566=
ENST00000442415.7:c.1758C>G (RAF1)	ENSP00000401888.2:p.Ala586=
ENST00000676541.1:c.*2699G>C (MKRN2)	ENSP00000503730.1:n.*2699G>C
ENST00000677142.1:c.*2699G>C (MKRN2)	ENSP00000504455.1:n.*2699G>C
ENST00000677816.1:c.*1254G>C (MKRN2)	ENSP00000502893.1:n.*1254G>C
ENST00000677941.1:n.2762G>C (MKRN2)
ENST00000251849.8:c.1698C>G (RAF1)	ENSP00000251849.4:p.Ala566=
ENST00000423275.5:c.*1375C>G (RAF1)	ENSP00000401088.1:n.*1375C>G
ENST00000432427.2:c.1335C>G (RAF1)	ENSP00000398591.2:p.Ala445=
ENST00000442415.6:c.1758C>G (RAF1)	ENSP00000401888.2:p.Ala586=
ENST00000471449.1:n.387C>G (RAF1)
NM_002880.3:c.1698C>G , LRG_413t1:c.1698C>G (RAF1)	NP_002871.1:p.Ala566=
XM_005265355.1:c.1698C>G (RAF1)	XP_005265412.1:p.Ala566=
XM_005265357.1:c.1599C>G (RAF1)	XP_005265414.1:p.Ala533=
XM_005265358.3:c.1455C>G (RAF1)	XP_005265415.1:p.Ala485=
XM_005265359.3:c.1356C>G (RAF1)	XP_005265416.1:p.Ala452=
XM_011533974.1:c.1698C>G (RAF1)	XP_011532276.1:p.Ala566=
XM_011533975.1:c.1455C>G (RAF1)	XP_011532277.1:p.Ala485=
NM_001354689.1:c.1758C>G (RAF1)	NP_001341618.1:p.Ala586=
NM_001354690.1:c.1698C>G (RAF1)	NP_001341619.1:p.Ala566=
NM_001354691.1:c.1455C>G (RAF1)	NP_001341620.1:p.Ala485=
NM_001354692.1:c.1455C>G (RAF1)	NP_001341621.1:p.Ala485=
NM_001354693.1:c.1599C>G (RAF1)	NP_001341622.1:p.Ala533=
NM_001354694.1:c.1515C>G (RAF1)	NP_001341623.1:p.Ala505=
NM_001354695.1:c.1356C>G (RAF1)	NP_001341624.1:p.Ala452=
NR_148940.1:n.2226C>G (RAF1)
NR_148941.1:n.2172C>G (RAF1)
NR_148942.1:n.2111C>G (RAF1)
XM_011533974.3:c.1698C>G (RAF1)	XP_011532276.1:p.Ala566=
XM_017006966.1:c.1599C>G (RAF1)	XP_016862455.1:p.Ala533=
NM_001354689.3:c.1758C>G (RAF1)	NP_001341618.1:p.Ala586=
NM_001354690.2:c.1698C>G (RAF1)	NP_001341619.1:p.Ala566=
NM_001354691.2:c.1455C>G (RAF1)	NP_001341620.1:p.Ala485=
NM_001354692.2:c.1455C>G (RAF1)	NP_001341621.1:p.Ala485=
NM_001354693.2:c.1599C>G (RAF1)	NP_001341622.1:p.Ala533=
NM_001354694.2:c.1515C>G (RAF1)	NP_001341623.1:p.Ala505=
NM_001354695.2:c.1356C>G (RAF1)	NP_001341624.1:p.Ala452=
NR_148940.2:n.2142C>G (RAF1)
NR_148941.2:n.2088C>G (RAF1)
NR_148942.2:n.2027C>G (RAF1)
NM_001354690.3:c.1698C>G (RAF1)	NP_001341619.1:p.Ala566=
NM_001354691.3:c.1455C>G (RAF1)	NP_001341620.1:p.Ala485=
NM_001354692.3:c.1455C>G (RAF1)	NP_001341621.1:p.Ala485=
NM_001354693.3:c.1599C>G (RAF1)	NP_001341622.1:p.Ala533=
NM_001354694.3:c.1515C>G (RAF1)	NP_001341623.1:p.Ala505=
NM_001354695.3:c.1356C>G (RAF1)	NP_001341624.1:p.Ala452=
NM_002880.4:c.1698C>G (RAF1) MANE Select	NP_002871.1:p.Ala566=
NR_148940.3:n.2142C>G (RAF1)
NR_148941.3:n.2088C>G (RAF1)
NR_148942.3:n.2027C>G (RAF1)