Canonical Allele Identifier: CA351496711

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626406C>A (hg19) ; chr3:g.12584907C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584907C>A , CM000665.2:g.12584907C>A	GRCh38
NC_000003.11:g.12626406C>A , CM000665.1:g.12626406C>A	GRCh37
NC_000003.10:g.12601406C>A	NCBI36
NG_007467.1:g.84273G>T , LRG_413:g.84273G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1408G>T (RAF1)	ENSP00000401088.1:n.*1408G>T
ENST00000432427.3:c.1060G>T (RAF1)
ENST00000460610.2:n.6055G>T (RAF1)
ENST00000471449.2:n.553G>T (RAF1)
ENST00000475353.2:n.4023G>T (RAF1)
ENST00000684903.1:c.*1420G>T (RAF1)	ENSP00000508612.1:n.*1420G>T
ENST00000685348.1:c.*1454G>T (RAF1)	ENSP00000510285.1:n.*1454G>T
ENST00000685437.1:c.1644G>T (RAF1)	ENSP00000508794.1:p.Met548Ile
ENST00000685653.1:c.1743G>T (RAF1)	ENSP00000509968.1:p.Met581Ile
ENST00000685697.1:n.2478G>T (RAF1)
ENST00000685738.1:c.*707G>T (RAF1)	ENSP00000510156.1:n.*707G>T
ENST00000686409.1:n.5152G>T (RAF1)
ENST00000686455.1:n.4464G>T (RAF1)
ENST00000686762.1:c.*302G>T (RAF1)	ENSP00000509767.1:n.*302G>T
ENST00000687257.1:n.4197G>T (RAF1)
ENST00000687326.1:c.*3035G>T (RAF1)	ENSP00000509665.1:n.*3035G>T
ENST00000687505.1:n.1861G>T (RAF1)
ENST00000687923.1:c.1632G>T (RAF1)	ENSP00000510255.1:p.Met544Ile
ENST00000688269.1:n.2339G>T (RAF1)
ENST00000688444.1:n.3860G>T (RAF1)
ENST00000688543.1:c.1644G>T (RAF1)	ENSP00000509612.1:p.Met548Ile
ENST00000688625.1:c.*3112G>T (RAF1)	ENSP00000509522.1:n.*3112G>T
ENST00000688803.1:n.3171G>T (RAF1)
ENST00000688914.1:n.1156G>T (RAF1)
ENST00000689097.1:c.*1420G>T (RAF1)	ENSP00000509756.1:n.*1420G>T
ENST00000689389.1:c.1566G>T (RAF1)	ENSP00000510213.1:p.Met522Ile
ENST00000689418.1:c.*3638G>T (RAF1)	ENSP00000509467.1:n.*3638G>T
ENST00000689540.1:n.4111G>T (RAF1)
ENST00000689876.1:c.*292G>T (RAF1)	ENSP00000508535.1:n.*292G>T
ENST00000689914.1:c.*677G>T (RAF1)	ENSP00000509847.1:n.*677G>T
ENST00000690397.1:c.1632G>T (RAF1)	ENSP00000508730.1:p.Met544Ile
ENST00000690460.1:c.1731G>T (RAF1)	ENSP00000509106.1:p.Met577Ile
ENST00000690585.1:c.469G>T (RAF1)
ENST00000690625.1:n.2779G>T (RAF1)
ENST00000691396.1:c.*1615G>T (RAF1)	ENSP00000510712.1:n.*1615G>T
ENST00000691643.1:n.2796G>T (RAF1)
ENST00000691724.1:c.*700G>T (RAF1)	ENSP00000509255.1:n.*700G>T
ENST00000691779.1:c.*1321G>T (RAF1)	ENSP00000508592.1:n.*1321G>T
ENST00000691888.1:c.617G>T (RAF1)
ENST00000691899.1:c.1743G>T (RAF1)	ENSP00000508763.1:p.Met581Ile
ENST00000692069.1:n.4667G>T (RAF1)
ENST00000692093.1:c.1644G>T (RAF1)	ENSP00000509669.1:p.Met548Ile
ENST00000692311.1:n.2567G>T (RAF1)
ENST00000692558.1:n.4326G>T (RAF1)
ENST00000692773.1:c.*1480G>T (RAF1)	ENSP00000509055.1:n.*1480G>T
ENST00000692830.1:c.*1488G>T (RAF1)	ENSP00000509461.1:n.*1488G>T
ENST00000693312.1:c.1518G>T (RAF1)	ENSP00000508686.1:p.Met506Ile
ENST00000693664.1:c.*194G>T (RAF1)	ENSP00000509614.1:n.*194G>T
ENST00000693705.1:c.*1122G>T (RAF1)	ENSP00000510697.1:n.*1122G>T
ENST00000251849.9:c.1743G>T (RAF1) MANE Select	ENSP00000251849.4:p.Met581Ile
ENST00000442415.7:c.1803G>T (RAF1)	ENSP00000401888.2:p.Met601Ile
ENST00000676541.1:c.*2654C>A (MKRN2)	ENSP00000503730.1:n.*2654C>A
ENST00000677142.1:c.*2654C>A (MKRN2)	ENSP00000504455.1:n.*2654C>A
ENST00000677816.1:c.*1209C>A (MKRN2)	ENSP00000502893.1:n.*1209C>A
ENST00000677941.1:n.2717C>A (MKRN2)
ENST00000251849.8:c.1743G>T (RAF1)	ENSP00000251849.4:p.Met581Ile
ENST00000423275.5:c.*1420G>T (RAF1)	ENSP00000401088.1:n.*1420G>T
ENST00000432427.2:c.1380G>T (RAF1)	ENSP00000398591.2:p.Met460Ile
ENST00000442415.6:c.1803G>T (RAF1)	ENSP00000401888.2:p.Met601Ile
ENST00000471449.1:n.432G>T (RAF1)
NM_002880.3:c.1743G>T , LRG_413t1:c.1743G>T (RAF1)	NP_002871.1:p.Met581Ile
XM_005265355.1:c.1743G>T (RAF1)	XP_005265412.1:p.Met581Ile
XM_005265357.1:c.1644G>T (RAF1)	XP_005265414.1:p.Met548Ile
XM_005265358.3:c.1500G>T (RAF1)	XP_005265415.1:p.Met500Ile
XM_005265359.3:c.1401G>T (RAF1)	XP_005265416.1:p.Met467Ile
XM_011533974.1:c.1743G>T (RAF1)	XP_011532276.1:p.Met581Ile
XM_011533975.1:c.1500G>T (RAF1)	XP_011532277.1:p.Met500Ile
NM_001354689.1:c.1803G>T (RAF1)	NP_001341618.1:p.Met601Ile
NM_001354690.1:c.1743G>T (RAF1)	NP_001341619.1:p.Met581Ile
NM_001354691.1:c.1500G>T (RAF1)	NP_001341620.1:p.Met500Ile
NM_001354692.1:c.1500G>T (RAF1)	NP_001341621.1:p.Met500Ile
NM_001354693.1:c.1644G>T (RAF1)	NP_001341622.1:p.Met548Ile
NM_001354694.1:c.1560G>T (RAF1)	NP_001341623.1:p.Met520Ile
NM_001354695.1:c.1401G>T (RAF1)	NP_001341624.1:p.Met467Ile
NR_148940.1:n.2271G>T (RAF1)
NR_148941.1:n.2217G>T (RAF1)
NR_148942.1:n.2156G>T (RAF1)
XM_011533974.3:c.1743G>T (RAF1)	XP_011532276.1:p.Met581Ile
XM_017006966.1:c.1644G>T (RAF1)	XP_016862455.1:p.Met548Ile
NM_001354689.3:c.1803G>T (RAF1)	NP_001341618.1:p.Met601Ile
NM_001354690.2:c.1743G>T (RAF1)	NP_001341619.1:p.Met581Ile
NM_001354691.2:c.1500G>T (RAF1)	NP_001341620.1:p.Met500Ile
NM_001354692.2:c.1500G>T (RAF1)	NP_001341621.1:p.Met500Ile
NM_001354693.2:c.1644G>T (RAF1)	NP_001341622.1:p.Met548Ile
NM_001354694.2:c.1560G>T (RAF1)	NP_001341623.1:p.Met520Ile
NM_001354695.2:c.1401G>T (RAF1)	NP_001341624.1:p.Met467Ile
NR_148940.2:n.2187G>T (RAF1)
NR_148941.2:n.2133G>T (RAF1)
NR_148942.2:n.2072G>T (RAF1)
NM_001354690.3:c.1743G>T (RAF1)	NP_001341619.1:p.Met581Ile
NM_001354691.3:c.1500G>T (RAF1)	NP_001341620.1:p.Met500Ile
NM_001354692.3:c.1500G>T (RAF1)	NP_001341621.1:p.Met500Ile
NM_001354693.3:c.1644G>T (RAF1)	NP_001341622.1:p.Met548Ile
NM_001354694.3:c.1560G>T (RAF1)	NP_001341623.1:p.Met520Ile
NM_001354695.3:c.1401G>T (RAF1)	NP_001341624.1:p.Met467Ile
NM_002880.4:c.1743G>T (RAF1) MANE Select	NP_002871.1:p.Met581Ile
NR_148940.3:n.2187G>T (RAF1)
NR_148941.3:n.2133G>T (RAF1)
NR_148942.3:n.2072G>T (RAF1)