Canonical Allele Identifier: CA432272626

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs148528418
• MyVariant Identifiers: chr3:g.12626037C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584538C>A , CM000665.2:g.12584538C>A	GRCh38
NC_000003.11:g.12626037C>A , CM000665.1:g.12626037C>A	GRCh37
NC_000003.10:g.12601037C>A	NCBI36
NG_007467.1:g.84642G>T , LRG_413:g.84642G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1588G>T (RAF1)	ENSP00000401088.1:n.*1588G>T
ENST00000432427.3:c.1240G>T (RAF1)
ENST00000460610.2:n.6235G>T (RAF1)
ENST00000471449.2:n.733G>T (RAF1)
ENST00000475353.2:n.4203G>T (RAF1)
ENST00000684903.1:c.*1600G>T (RAF1)	ENSP00000508612.1:n.*1600G>T
ENST00000685348.1:c.*1634G>T (RAF1)	ENSP00000510285.1:n.*1634G>T
ENST00000685437.1:c.1824G>T (RAF1)	ENSP00000508794.1:p.Thr608=
ENST00000685653.1:c.1923G>T (RAF1)	ENSP00000509968.1:p.Thr641=
ENST00000685697.1:n.2658G>T (RAF1)
ENST00000685738.1:c.*887G>T (RAF1)	ENSP00000510156.1:n.*887G>T
ENST00000686409.1:n.5332G>T (RAF1)
ENST00000686455.1:n.4644G>T (RAF1)
ENST00000686762.1:c.*482G>T (RAF1)	ENSP00000509767.1:n.*482G>T
ENST00000687257.1:n.4377G>T (RAF1)
ENST00000687326.1:c.*3215G>T (RAF1)	ENSP00000509665.1:n.*3215G>T
ENST00000687505.1:n.2041G>T (RAF1)
ENST00000687923.1:c.1812G>T (RAF1)	ENSP00000510255.1:p.Thr604=
ENST00000688269.1:n.2519G>T (RAF1)
ENST00000688444.1:n.4040G>T (RAF1)
ENST00000688543.1:c.1824G>T (RAF1)	ENSP00000509612.1:p.Thr608=
ENST00000688625.1:c.*3292G>T (RAF1)	ENSP00000509522.1:n.*3292G>T
ENST00000688803.1:n.3351G>T (RAF1)
ENST00000689097.1:c.*1600G>T (RAF1)	ENSP00000509756.1:n.*1600G>T
ENST00000689389.1:c.1746G>T (RAF1)	ENSP00000510213.1:p.Thr582=
ENST00000689418.1:c.*3818G>T (RAF1)	ENSP00000509467.1:n.*3818G>T
ENST00000689540.1:n.4291G>T (RAF1)
ENST00000689876.1:c.*472G>T (RAF1)	ENSP00000508535.1:n.*472G>T
ENST00000689914.1:c.*857G>T (RAF1)	ENSP00000509847.1:n.*857G>T
ENST00000690397.1:c.1812G>T (RAF1)	ENSP00000508730.1:p.Thr604=
ENST00000690460.1:c.1911G>T (RAF1)	ENSP00000509106.1:p.Thr637=
ENST00000690585.1:c.649G>T (RAF1)
ENST00000690625.1:n.2959G>T (RAF1)
ENST00000691396.1:c.*1795G>T (RAF1)	ENSP00000510712.1:n.*1795G>T
ENST00000691643.1:n.2976G>T (RAF1)
ENST00000691724.1:c.*880G>T (RAF1)	ENSP00000509255.1:n.*880G>T
ENST00000691779.1:c.*1501G>T (RAF1)	ENSP00000508592.1:n.*1501G>T
ENST00000691888.1:c.797G>T (RAF1)
ENST00000691899.1:c.1923G>T (RAF1)	ENSP00000508763.1:p.Thr641=
ENST00000692069.1:n.4847G>T (RAF1)
ENST00000692093.1:c.1824G>T (RAF1)	ENSP00000509669.1:p.Thr608=
ENST00000692311.1:n.2747G>T (RAF1)
ENST00000692558.1:n.4506G>T (RAF1)
ENST00000692773.1:c.*1660G>T (RAF1)	ENSP00000509055.1:n.*1660G>T
ENST00000692830.1:c.*1668G>T (RAF1)	ENSP00000509461.1:n.*1668G>T
ENST00000693312.1:c.1698G>T (RAF1)	ENSP00000508686.1:p.Thr566=
ENST00000693664.1:c.*374G>T (RAF1)	ENSP00000509614.1:n.*374G>T
ENST00000693705.1:c.*1302G>T (RAF1)	ENSP00000510697.1:n.*1302G>T
ENST00000251849.9:c.1923G>T (RAF1) MANE Select	ENSP00000251849.4:p.Thr641=
ENST00000442415.7:c.1983G>T (RAF1)	ENSP00000401888.2:p.Thr661=
ENST00000676541.1:c.*2285C>A (MKRN2)	ENSP00000503730.1:n.*2285C>A
ENST00000677142.1:c.*2285C>A (MKRN2)	ENSP00000504455.1:n.*2285C>A
ENST00000677816.1:c.*840C>A (MKRN2)	ENSP00000502893.1:n.*840C>A
ENST00000677941.1:n.2348C>A (MKRN2)
ENST00000251849.8:c.1923G>T (RAF1)	ENSP00000251849.4:p.Thr641=
ENST00000423275.5:c.*1600G>T (RAF1)	ENSP00000401088.1:n.*1600G>T
ENST00000432427.2:c.1560G>T (RAF1)	ENSP00000398591.2:p.Thr520=
ENST00000442415.6:c.1983G>T (RAF1)	ENSP00000401888.2:p.Thr661=
ENST00000471449.1:n.612G>T (RAF1)
NM_002880.3:c.1923G>T , LRG_413t1:c.1923G>T (RAF1)	NP_002871.1:p.Thr641=
XM_005265355.1:c.1923G>T (RAF1)	XP_005265412.1:p.Thr641=
XM_005265357.1:c.1824G>T (RAF1)	XP_005265414.1:p.Thr608=
XM_005265358.3:c.1680G>T (RAF1)	XP_005265415.1:p.Thr560=
XM_005265359.3:c.1581G>T (RAF1)	XP_005265416.1:p.Thr527=
XM_011533974.1:c.1923G>T (RAF1)	XP_011532276.1:p.Thr641=
XM_011533975.1:c.1680G>T (RAF1)	XP_011532277.1:p.Thr560=
NM_001354689.1:c.1983G>T (RAF1)	NP_001341618.1:p.Thr661=
NM_001354690.1:c.1923G>T (RAF1)	NP_001341619.1:p.Thr641=
NM_001354691.1:c.1680G>T (RAF1)	NP_001341620.1:p.Thr560=
NM_001354692.1:c.1680G>T (RAF1)	NP_001341621.1:p.Thr560=
NM_001354693.1:c.1824G>T (RAF1)	NP_001341622.1:p.Thr608=
NM_001354694.1:c.1740G>T (RAF1)	NP_001341623.1:p.Thr580=
NM_001354695.1:c.1581G>T (RAF1)	NP_001341624.1:p.Thr527=
NR_148940.1:n.2451G>T (RAF1)
NR_148941.1:n.2397G>T (RAF1)
NR_148942.1:n.2336G>T (RAF1)
XM_011533974.3:c.1923G>T (RAF1)	XP_011532276.1:p.Thr641=
XM_017006966.1:c.1824G>T (RAF1)	XP_016862455.1:p.Thr608=
NM_001354689.3:c.1983G>T (RAF1)	NP_001341618.1:p.Thr661=
NM_001354690.2:c.1923G>T (RAF1)	NP_001341619.1:p.Thr641=
NM_001354691.2:c.1680G>T (RAF1)	NP_001341620.1:p.Thr560=
NM_001354692.2:c.1680G>T (RAF1)	NP_001341621.1:p.Thr560=
NM_001354693.2:c.1824G>T (RAF1)	NP_001341622.1:p.Thr608=
NM_001354694.2:c.1740G>T (RAF1)	NP_001341623.1:p.Thr580=
NM_001354695.2:c.1581G>T (RAF1)	NP_001341624.1:p.Thr527=
NR_148940.2:n.2367G>T (RAF1)
NR_148941.2:n.2313G>T (RAF1)
NR_148942.2:n.2252G>T (RAF1)
NM_001354690.3:c.1923G>T (RAF1)	NP_001341619.1:p.Thr641=
NM_001354691.3:c.1680G>T (RAF1)	NP_001341620.1:p.Thr560=
NM_001354692.3:c.1680G>T (RAF1)	NP_001341621.1:p.Thr560=
NM_001354693.3:c.1824G>T (RAF1)	NP_001341622.1:p.Thr608=
NM_001354694.3:c.1740G>T (RAF1)	NP_001341623.1:p.Thr580=
NM_001354695.3:c.1581G>T (RAF1)	NP_001341624.1:p.Thr527=
NM_002880.4:c.1923G>T (RAF1) MANE Select	NP_002871.1:p.Thr641=
NR_148940.3:n.2367G>T (RAF1)
NR_148941.3:n.2313G>T (RAF1)
NR_148942.3:n.2252G>T (RAF1)