Canonical Allele Identifier: CA351495844

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626093G>T (hg19) ; chr3:g.12584594G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584594G>T , CM000665.2:g.12584594G>T	GRCh38
NC_000003.11:g.12626093G>T , CM000665.1:g.12626093G>T	GRCh37
NC_000003.10:g.12601093G>T	NCBI36
NG_007467.1:g.84586C>A , LRG_413:g.84586C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1532C>A (RAF1)	ENSP00000401088.1:n.*1532C>A
ENST00000432427.3:c.1184C>A (RAF1)
ENST00000460610.2:n.6179C>A (RAF1)
ENST00000471449.2:n.677C>A (RAF1)
ENST00000475353.2:n.4147C>A (RAF1)
ENST00000684903.1:c.*1544C>A (RAF1)	ENSP00000508612.1:n.*1544C>A
ENST00000685348.1:c.*1578C>A (RAF1)	ENSP00000510285.1:n.*1578C>A
ENST00000685437.1:c.1768C>A (RAF1)	ENSP00000508794.1:p.Pro590Thr
ENST00000685653.1:c.1867C>A (RAF1)	ENSP00000509968.1:p.Pro623Thr
ENST00000685697.1:n.2602C>A (RAF1)
ENST00000685738.1:c.*831C>A (RAF1)	ENSP00000510156.1:n.*831C>A
ENST00000686409.1:n.5276C>A (RAF1)
ENST00000686455.1:n.4588C>A (RAF1)
ENST00000686762.1:c.*426C>A (RAF1)	ENSP00000509767.1:n.*426C>A
ENST00000687257.1:n.4321C>A (RAF1)
ENST00000687326.1:c.*3159C>A (RAF1)	ENSP00000509665.1:n.*3159C>A
ENST00000687505.1:n.1985C>A (RAF1)
ENST00000687923.1:c.1756C>A (RAF1)	ENSP00000510255.1:p.Pro586Thr
ENST00000688269.1:n.2463C>A (RAF1)
ENST00000688444.1:n.3984C>A (RAF1)
ENST00000688543.1:c.1768C>A (RAF1)	ENSP00000509612.1:p.Pro590Thr
ENST00000688625.1:c.*3236C>A (RAF1)	ENSP00000509522.1:n.*3236C>A
ENST00000688803.1:n.3295C>A (RAF1)
ENST00000689097.1:c.*1544C>A (RAF1)	ENSP00000509756.1:n.*1544C>A
ENST00000689389.1:c.1690C>A (RAF1)	ENSP00000510213.1:p.Pro564Thr
ENST00000689418.1:c.*3762C>A (RAF1)	ENSP00000509467.1:n.*3762C>A
ENST00000689540.1:n.4235C>A (RAF1)
ENST00000689876.1:c.*416C>A (RAF1)	ENSP00000508535.1:n.*416C>A
ENST00000689914.1:c.*801C>A (RAF1)	ENSP00000509847.1:n.*801C>A
ENST00000690397.1:c.1756C>A (RAF1)	ENSP00000508730.1:p.Pro586Thr
ENST00000690460.1:c.1855C>A (RAF1)	ENSP00000509106.1:p.Pro619Thr
ENST00000690585.1:c.593C>A (RAF1)
ENST00000690625.1:n.2903C>A (RAF1)
ENST00000691396.1:c.*1739C>A (RAF1)	ENSP00000510712.1:n.*1739C>A
ENST00000691643.1:n.2920C>A (RAF1)
ENST00000691724.1:c.*824C>A (RAF1)	ENSP00000509255.1:n.*824C>A
ENST00000691779.1:c.*1445C>A (RAF1)	ENSP00000508592.1:n.*1445C>A
ENST00000691888.1:c.741C>A (RAF1)
ENST00000691899.1:c.1867C>A (RAF1)	ENSP00000508763.1:p.Pro623Thr
ENST00000692069.1:n.4791C>A (RAF1)
ENST00000692093.1:c.1768C>A (RAF1)	ENSP00000509669.1:p.Pro590Thr
ENST00000692311.1:n.2691C>A (RAF1)
ENST00000692558.1:n.4450C>A (RAF1)
ENST00000692773.1:c.*1604C>A (RAF1)	ENSP00000509055.1:n.*1604C>A
ENST00000692830.1:c.*1612C>A (RAF1)	ENSP00000509461.1:n.*1612C>A
ENST00000693312.1:c.1642C>A (RAF1)	ENSP00000508686.1:p.Pro548Thr
ENST00000693664.1:c.*318C>A (RAF1)	ENSP00000509614.1:n.*318C>A
ENST00000693705.1:c.*1246C>A (RAF1)	ENSP00000510697.1:n.*1246C>A
ENST00000251849.9:c.1867C>A (RAF1) MANE Select	ENSP00000251849.4:p.Pro623Thr
ENST00000442415.7:c.1927C>A (RAF1)	ENSP00000401888.2:p.Pro643Thr
ENST00000676541.1:c.*2341G>T (MKRN2)	ENSP00000503730.1:n.*2341G>T
ENST00000677142.1:c.*2341G>T (MKRN2)	ENSP00000504455.1:n.*2341G>T
ENST00000677816.1:c.*896G>T (MKRN2)	ENSP00000502893.1:n.*896G>T
ENST00000677941.1:n.2404G>T (MKRN2)
ENST00000251849.8:c.1867C>A (RAF1)	ENSP00000251849.4:p.Pro623Thr
ENST00000423275.5:c.*1544C>A (RAF1)	ENSP00000401088.1:n.*1544C>A
ENST00000432427.2:c.1504C>A (RAF1)	ENSP00000398591.2:p.Pro502Thr
ENST00000442415.6:c.1927C>A (RAF1)	ENSP00000401888.2:p.Pro643Thr
ENST00000471449.1:n.556C>A (RAF1)
NM_002880.3:c.1867C>A , LRG_413t1:c.1867C>A (RAF1)	NP_002871.1:p.Pro623Thr
XM_005265355.1:c.1867C>A (RAF1)	XP_005265412.1:p.Pro623Thr
XM_005265357.1:c.1768C>A (RAF1)	XP_005265414.1:p.Pro590Thr
XM_005265358.3:c.1624C>A (RAF1)	XP_005265415.1:p.Pro542Thr
XM_005265359.3:c.1525C>A (RAF1)	XP_005265416.1:p.Pro509Thr
XM_011533974.1:c.1867C>A (RAF1)	XP_011532276.1:p.Pro623Thr
XM_011533975.1:c.1624C>A (RAF1)	XP_011532277.1:p.Pro542Thr
NM_001354689.1:c.1927C>A (RAF1)	NP_001341618.1:p.Pro643Thr
NM_001354690.1:c.1867C>A (RAF1)	NP_001341619.1:p.Pro623Thr
NM_001354691.1:c.1624C>A (RAF1)	NP_001341620.1:p.Pro542Thr
NM_001354692.1:c.1624C>A (RAF1)	NP_001341621.1:p.Pro542Thr
NM_001354693.1:c.1768C>A (RAF1)	NP_001341622.1:p.Pro590Thr
NM_001354694.1:c.1684C>A (RAF1)	NP_001341623.1:p.Pro562Thr
NM_001354695.1:c.1525C>A (RAF1)	NP_001341624.1:p.Pro509Thr
NR_148940.1:n.2395C>A (RAF1)
NR_148941.1:n.2341C>A (RAF1)
NR_148942.1:n.2280C>A (RAF1)
XM_011533974.3:c.1867C>A (RAF1)	XP_011532276.1:p.Pro623Thr
XM_017006966.1:c.1768C>A (RAF1)	XP_016862455.1:p.Pro590Thr
NM_001354689.3:c.1927C>A (RAF1)	NP_001341618.1:p.Pro643Thr
NM_001354690.2:c.1867C>A (RAF1)	NP_001341619.1:p.Pro623Thr
NM_001354691.2:c.1624C>A (RAF1)	NP_001341620.1:p.Pro542Thr
NM_001354692.2:c.1624C>A (RAF1)	NP_001341621.1:p.Pro542Thr
NM_001354693.2:c.1768C>A (RAF1)	NP_001341622.1:p.Pro590Thr
NM_001354694.2:c.1684C>A (RAF1)	NP_001341623.1:p.Pro562Thr
NM_001354695.2:c.1525C>A (RAF1)	NP_001341624.1:p.Pro509Thr
NR_148940.2:n.2311C>A (RAF1)
NR_148941.2:n.2257C>A (RAF1)
NR_148942.2:n.2196C>A (RAF1)
NM_001354690.3:c.1867C>A (RAF1)	NP_001341619.1:p.Pro623Thr
NM_001354691.3:c.1624C>A (RAF1)	NP_001341620.1:p.Pro542Thr
NM_001354692.3:c.1624C>A (RAF1)	NP_001341621.1:p.Pro542Thr
NM_001354693.3:c.1768C>A (RAF1)	NP_001341622.1:p.Pro590Thr
NM_001354694.3:c.1684C>A (RAF1)	NP_001341623.1:p.Pro562Thr
NM_001354695.3:c.1525C>A (RAF1)	NP_001341624.1:p.Pro509Thr
NM_002880.4:c.1867C>A (RAF1) MANE Select	NP_002871.1:p.Pro623Thr
NR_148940.3:n.2311C>A (RAF1)
NR_148941.3:n.2257C>A (RAF1)
NR_148942.3:n.2196C>A (RAF1)