Canonical Allele Identifier: CA432272719

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs146561613
• MyVariant Identifiers: chr3:g.12626148A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584649A>G , CM000665.2:g.12584649A>G	GRCh38
NC_000003.11:g.12626148A>G , CM000665.1:g.12626148A>G	GRCh37
NC_000003.10:g.12601148A>G	NCBI36
NG_007467.1:g.84531T>C , LRG_413:g.84531T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1477T>C (RAF1)	ENSP00000401088.1:n.*1477T>C
ENST00000432427.3:c.1129T>C (RAF1)
ENST00000460610.2:n.6124T>C (RAF1)
ENST00000471449.2:n.622T>C (RAF1)
ENST00000475353.2:n.4092T>C (RAF1)
ENST00000684903.1:c.*1489T>C (RAF1)	ENSP00000508612.1:n.*1489T>C
ENST00000685348.1:c.*1523T>C (RAF1)	ENSP00000510285.1:n.*1523T>C
ENST00000685437.1:c.1713T>C (RAF1)	ENSP00000508794.1:p.Ser571=
ENST00000685653.1:c.1812T>C (RAF1)	ENSP00000509968.1:p.Ser604=
ENST00000685697.1:n.2547T>C (RAF1)
ENST00000685738.1:c.*776T>C (RAF1)	ENSP00000510156.1:n.*776T>C
ENST00000686409.1:n.5221T>C (RAF1)
ENST00000686455.1:n.4533T>C (RAF1)
ENST00000686762.1:c.*371T>C (RAF1)	ENSP00000509767.1:n.*371T>C
ENST00000687257.1:n.4266T>C (RAF1)
ENST00000687326.1:c.*3104T>C (RAF1)	ENSP00000509665.1:n.*3104T>C
ENST00000687505.1:n.1930T>C (RAF1)
ENST00000687923.1:c.1701T>C (RAF1)	ENSP00000510255.1:p.Ser567=
ENST00000688269.1:n.2408T>C (RAF1)
ENST00000688444.1:n.3929T>C (RAF1)
ENST00000688543.1:c.1713T>C (RAF1)	ENSP00000509612.1:p.Ser571=
ENST00000688625.1:c.*3181T>C (RAF1)	ENSP00000509522.1:n.*3181T>C
ENST00000688803.1:n.3240T>C (RAF1)
ENST00000689097.1:c.*1489T>C (RAF1)	ENSP00000509756.1:n.*1489T>C
ENST00000689389.1:c.1635T>C (RAF1)	ENSP00000510213.1:p.Ser545=
ENST00000689418.1:c.*3707T>C (RAF1)	ENSP00000509467.1:n.*3707T>C
ENST00000689540.1:n.4180T>C (RAF1)
ENST00000689876.1:c.*361T>C (RAF1)	ENSP00000508535.1:n.*361T>C
ENST00000689914.1:c.*746T>C (RAF1)	ENSP00000509847.1:n.*746T>C
ENST00000690397.1:c.1701T>C (RAF1)	ENSP00000508730.1:p.Ser567=
ENST00000690460.1:c.1800T>C (RAF1)	ENSP00000509106.1:p.Ser600=
ENST00000690585.1:c.538T>C (RAF1)
ENST00000690625.1:n.2848T>C (RAF1)
ENST00000691396.1:c.*1684T>C (RAF1)	ENSP00000510712.1:n.*1684T>C
ENST00000691643.1:n.2865T>C (RAF1)
ENST00000691724.1:c.*769T>C (RAF1)	ENSP00000509255.1:n.*769T>C
ENST00000691779.1:c.*1390T>C (RAF1)	ENSP00000508592.1:n.*1390T>C
ENST00000691888.1:c.686T>C (RAF1)
ENST00000691899.1:c.1812T>C (RAF1)	ENSP00000508763.1:p.Ser604=
ENST00000692069.1:n.4736T>C (RAF1)
ENST00000692093.1:c.1713T>C (RAF1)	ENSP00000509669.1:p.Ser571=
ENST00000692311.1:n.2636T>C (RAF1)
ENST00000692558.1:n.4395T>C (RAF1)
ENST00000692773.1:c.*1549T>C (RAF1)	ENSP00000509055.1:n.*1549T>C
ENST00000692830.1:c.*1557T>C (RAF1)	ENSP00000509461.1:n.*1557T>C
ENST00000693312.1:c.1587T>C (RAF1)	ENSP00000508686.1:p.Ser529=
ENST00000693664.1:c.*263T>C (RAF1)	ENSP00000509614.1:n.*263T>C
ENST00000693705.1:c.*1191T>C (RAF1)	ENSP00000510697.1:n.*1191T>C
ENST00000251849.9:c.1812T>C (RAF1) MANE Select	ENSP00000251849.4:p.Ser604=
ENST00000442415.7:c.1872T>C (RAF1)	ENSP00000401888.2:p.Ser624=
ENST00000676541.1:c.*2396A>G (MKRN2)	ENSP00000503730.1:n.*2396A>G
ENST00000677142.1:c.*2396A>G (MKRN2)	ENSP00000504455.1:n.*2396A>G
ENST00000677816.1:c.*951A>G (MKRN2)	ENSP00000502893.1:n.*951A>G
ENST00000677941.1:n.2459A>G (MKRN2)
ENST00000251849.8:c.1812T>C (RAF1)	ENSP00000251849.4:p.Ser604=
ENST00000423275.5:c.*1489T>C (RAF1)	ENSP00000401088.1:n.*1489T>C
ENST00000432427.2:c.1449T>C (RAF1)	ENSP00000398591.2:p.Ser483=
ENST00000442415.6:c.1872T>C (RAF1)	ENSP00000401888.2:p.Ser624=
ENST00000471449.1:n.501T>C (RAF1)
NM_002880.3:c.1812T>C , LRG_413t1:c.1812T>C (RAF1)	NP_002871.1:p.Ser604=
XM_005265355.1:c.1812T>C (RAF1)	XP_005265412.1:p.Ser604=
XM_005265357.1:c.1713T>C (RAF1)	XP_005265414.1:p.Ser571=
XM_005265358.3:c.1569T>C (RAF1)	XP_005265415.1:p.Ser523=
XM_005265359.3:c.1470T>C (RAF1)	XP_005265416.1:p.Ser490=
XM_011533974.1:c.1812T>C (RAF1)	XP_011532276.1:p.Ser604=
XM_011533975.1:c.1569T>C (RAF1)	XP_011532277.1:p.Ser523=
NM_001354689.1:c.1872T>C (RAF1)	NP_001341618.1:p.Ser624=
NM_001354690.1:c.1812T>C (RAF1)	NP_001341619.1:p.Ser604=
NM_001354691.1:c.1569T>C (RAF1)	NP_001341620.1:p.Ser523=
NM_001354692.1:c.1569T>C (RAF1)	NP_001341621.1:p.Ser523=
NM_001354693.1:c.1713T>C (RAF1)	NP_001341622.1:p.Ser571=
NM_001354694.1:c.1629T>C (RAF1)	NP_001341623.1:p.Ser543=
NM_001354695.1:c.1470T>C (RAF1)	NP_001341624.1:p.Ser490=
NR_148940.1:n.2340T>C (RAF1)
NR_148941.1:n.2286T>C (RAF1)
NR_148942.1:n.2225T>C (RAF1)
XM_011533974.3:c.1812T>C (RAF1)	XP_011532276.1:p.Ser604=
XM_017006966.1:c.1713T>C (RAF1)	XP_016862455.1:p.Ser571=
NM_001354689.3:c.1872T>C (RAF1)	NP_001341618.1:p.Ser624=
NM_001354690.2:c.1812T>C (RAF1)	NP_001341619.1:p.Ser604=
NM_001354691.2:c.1569T>C (RAF1)	NP_001341620.1:p.Ser523=
NM_001354692.2:c.1569T>C (RAF1)	NP_001341621.1:p.Ser523=
NM_001354693.2:c.1713T>C (RAF1)	NP_001341622.1:p.Ser571=
NM_001354694.2:c.1629T>C (RAF1)	NP_001341623.1:p.Ser543=
NM_001354695.2:c.1470T>C (RAF1)	NP_001341624.1:p.Ser490=
NR_148940.2:n.2256T>C (RAF1)
NR_148941.2:n.2202T>C (RAF1)
NR_148942.2:n.2141T>C (RAF1)
NM_001354690.3:c.1812T>C (RAF1)	NP_001341619.1:p.Ser604=
NM_001354691.3:c.1569T>C (RAF1)	NP_001341620.1:p.Ser523=
NM_001354692.3:c.1569T>C (RAF1)	NP_001341621.1:p.Ser523=
NM_001354693.3:c.1713T>C (RAF1)	NP_001341622.1:p.Ser571=
NM_001354694.3:c.1629T>C (RAF1)	NP_001341623.1:p.Ser543=
NM_001354695.3:c.1470T>C (RAF1)	NP_001341624.1:p.Ser490=
NM_002880.4:c.1812T>C (RAF1) MANE Select	NP_002871.1:p.Ser604=
NR_148940.3:n.2256T>C (RAF1)
NR_148941.3:n.2202T>C (RAF1)
NR_148942.3:n.2141T>C (RAF1)