Canonical Allele Identifier: CA351496836

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626434T>G (hg19) ; chr3:g.12584935T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584935T>G , CM000665.2:g.12584935T>G	GRCh38
NC_000003.11:g.12626434T>G , CM000665.1:g.12626434T>G	GRCh37
NC_000003.10:g.12601434T>G	NCBI36
NG_007467.1:g.84245A>C , LRG_413:g.84245A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1380A>C (RAF1)	ENSP00000401088.1:n.*1380A>C
ENST00000432427.3:c.1032A>C (RAF1)
ENST00000460610.2:n.6027A>C (RAF1)
ENST00000471449.2:n.525A>C (RAF1)
ENST00000475353.2:n.3995A>C (RAF1)
ENST00000684903.1:c.*1392A>C (RAF1)	ENSP00000508612.1:n.*1392A>C
ENST00000685348.1:c.*1426A>C (RAF1)	ENSP00000510285.1:n.*1426A>C
ENST00000685437.1:c.1616A>C (RAF1)	ENSP00000508794.1:p.Lys539Thr
ENST00000685653.1:c.1715A>C (RAF1)	ENSP00000509968.1:p.Lys572Thr
ENST00000685697.1:n.2450A>C (RAF1)
ENST00000685738.1:c.*679A>C (RAF1)	ENSP00000510156.1:n.*679A>C
ENST00000686409.1:n.5124A>C (RAF1)
ENST00000686455.1:n.4436A>C (RAF1)
ENST00000686762.1:c.*274A>C (RAF1)	ENSP00000509767.1:n.*274A>C
ENST00000687257.1:n.4169A>C (RAF1)
ENST00000687326.1:c.*3007A>C (RAF1)	ENSP00000509665.1:n.*3007A>C
ENST00000687505.1:n.1833A>C (RAF1)
ENST00000687923.1:c.1604A>C (RAF1)	ENSP00000510255.1:p.Lys535Thr
ENST00000688269.1:n.2311A>C (RAF1)
ENST00000688444.1:n.3832A>C (RAF1)
ENST00000688543.1:c.1616A>C (RAF1)	ENSP00000509612.1:p.Lys539Thr
ENST00000688625.1:c.*3084A>C (RAF1)	ENSP00000509522.1:n.*3084A>C
ENST00000688803.1:n.3143A>C (RAF1)
ENST00000688914.1:n.1128A>C (RAF1)
ENST00000689097.1:c.*1392A>C (RAF1)	ENSP00000509756.1:n.*1392A>C
ENST00000689389.1:c.1538A>C (RAF1)	ENSP00000510213.1:p.Lys513Thr
ENST00000689418.1:c.*3610A>C (RAF1)	ENSP00000509467.1:n.*3610A>C
ENST00000689540.1:n.4083A>C (RAF1)
ENST00000689876.1:c.*264A>C (RAF1)	ENSP00000508535.1:n.*264A>C
ENST00000689914.1:c.*649A>C (RAF1)	ENSP00000509847.1:n.*649A>C
ENST00000690397.1:c.1604A>C (RAF1)	ENSP00000508730.1:p.Lys535Thr
ENST00000690460.1:c.1703A>C (RAF1)	ENSP00000509106.1:p.Lys568Thr
ENST00000690585.1:c.441A>C (RAF1)
ENST00000690625.1:n.2751A>C (RAF1)
ENST00000691396.1:c.*1587A>C (RAF1)	ENSP00000510712.1:n.*1587A>C
ENST00000691643.1:n.2768A>C (RAF1)
ENST00000691724.1:c.*672A>C (RAF1)	ENSP00000509255.1:n.*672A>C
ENST00000691779.1:c.*1293A>C (RAF1)	ENSP00000508592.1:n.*1293A>C
ENST00000691888.1:c.589A>C (RAF1)
ENST00000691899.1:c.1715A>C (RAF1)	ENSP00000508763.1:p.Lys572Thr
ENST00000692069.1:n.4639A>C (RAF1)
ENST00000692093.1:c.1616A>C (RAF1)	ENSP00000509669.1:p.Lys539Thr
ENST00000692311.1:n.2539A>C (RAF1)
ENST00000692558.1:n.4298A>C (RAF1)
ENST00000692773.1:c.*1452A>C (RAF1)	ENSP00000509055.1:n.*1452A>C
ENST00000692830.1:c.*1460A>C (RAF1)	ENSP00000509461.1:n.*1460A>C
ENST00000693312.1:c.1490A>C (RAF1)	ENSP00000508686.1:p.Lys497Thr
ENST00000693664.1:c.*166A>C (RAF1)	ENSP00000509614.1:n.*166A>C
ENST00000693705.1:c.*1094A>C (RAF1)	ENSP00000510697.1:n.*1094A>C
ENST00000251849.9:c.1715A>C (RAF1) MANE Select	ENSP00000251849.4:p.Lys572Thr
ENST00000442415.7:c.1775A>C (RAF1)	ENSP00000401888.2:p.Lys592Thr
ENST00000676541.1:c.*2682T>G (MKRN2)	ENSP00000503730.1:n.*2682T>G
ENST00000677142.1:c.*2682T>G (MKRN2)	ENSP00000504455.1:n.*2682T>G
ENST00000677816.1:c.*1237T>G (MKRN2)	ENSP00000502893.1:n.*1237T>G
ENST00000677941.1:n.2745T>G (MKRN2)
ENST00000251849.8:c.1715A>C (RAF1)	ENSP00000251849.4:p.Lys572Thr
ENST00000423275.5:c.*1392A>C (RAF1)	ENSP00000401088.1:n.*1392A>C
ENST00000432427.2:c.1352A>C (RAF1)	ENSP00000398591.2:p.Lys451Thr
ENST00000442415.6:c.1775A>C (RAF1)	ENSP00000401888.2:p.Lys592Thr
ENST00000471449.1:n.404A>C (RAF1)
NM_002880.3:c.1715A>C , LRG_413t1:c.1715A>C (RAF1)	NP_002871.1:p.Lys572Thr
XM_005265355.1:c.1715A>C (RAF1)	XP_005265412.1:p.Lys572Thr
XM_005265357.1:c.1616A>C (RAF1)	XP_005265414.1:p.Lys539Thr
XM_005265358.3:c.1472A>C (RAF1)	XP_005265415.1:p.Lys491Thr
XM_005265359.3:c.1373A>C (RAF1)	XP_005265416.1:p.Lys458Thr
XM_011533974.1:c.1715A>C (RAF1)	XP_011532276.1:p.Lys572Thr
XM_011533975.1:c.1472A>C (RAF1)	XP_011532277.1:p.Lys491Thr
NM_001354689.1:c.1775A>C (RAF1)	NP_001341618.1:p.Lys592Thr
NM_001354690.1:c.1715A>C (RAF1)	NP_001341619.1:p.Lys572Thr
NM_001354691.1:c.1472A>C (RAF1)	NP_001341620.1:p.Lys491Thr
NM_001354692.1:c.1472A>C (RAF1)	NP_001341621.1:p.Lys491Thr
NM_001354693.1:c.1616A>C (RAF1)	NP_001341622.1:p.Lys539Thr
NM_001354694.1:c.1532A>C (RAF1)	NP_001341623.1:p.Lys511Thr
NM_001354695.1:c.1373A>C (RAF1)	NP_001341624.1:p.Lys458Thr
NR_148940.1:n.2243A>C (RAF1)
NR_148941.1:n.2189A>C (RAF1)
NR_148942.1:n.2128A>C (RAF1)
XM_011533974.3:c.1715A>C (RAF1)	XP_011532276.1:p.Lys572Thr
XM_017006966.1:c.1616A>C (RAF1)	XP_016862455.1:p.Lys539Thr
NM_001354689.3:c.1775A>C (RAF1)	NP_001341618.1:p.Lys592Thr
NM_001354690.2:c.1715A>C (RAF1)	NP_001341619.1:p.Lys572Thr
NM_001354691.2:c.1472A>C (RAF1)	NP_001341620.1:p.Lys491Thr
NM_001354692.2:c.1472A>C (RAF1)	NP_001341621.1:p.Lys491Thr
NM_001354693.2:c.1616A>C (RAF1)	NP_001341622.1:p.Lys539Thr
NM_001354694.2:c.1532A>C (RAF1)	NP_001341623.1:p.Lys511Thr
NM_001354695.2:c.1373A>C (RAF1)	NP_001341624.1:p.Lys458Thr
NR_148940.2:n.2159A>C (RAF1)
NR_148941.2:n.2105A>C (RAF1)
NR_148942.2:n.2044A>C (RAF1)
NM_001354690.3:c.1715A>C (RAF1)	NP_001341619.1:p.Lys572Thr
NM_001354691.3:c.1472A>C (RAF1)	NP_001341620.1:p.Lys491Thr
NM_001354692.3:c.1472A>C (RAF1)	NP_001341621.1:p.Lys491Thr
NM_001354693.3:c.1616A>C (RAF1)	NP_001341622.1:p.Lys539Thr
NM_001354694.3:c.1532A>C (RAF1)	NP_001341623.1:p.Lys511Thr
NM_001354695.3:c.1373A>C (RAF1)	NP_001341624.1:p.Lys458Thr
NM_002880.4:c.1715A>C (RAF1) MANE Select	NP_002871.1:p.Lys572Thr
NR_148940.3:n.2159A>C (RAF1)
NR_148941.3:n.2105A>C (RAF1)
NR_148942.3:n.2044A>C (RAF1)