Canonical Allele Identifier: CA432522005

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626373T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584874T>C , CM000665.2:g.12584874T>C	GRCh38
NC_000003.11:g.12626373T>C , CM000665.1:g.12626373T>C	GRCh37
NC_000003.10:g.12601373T>C	NCBI36
NG_007467.1:g.84306A>G , LRG_413:g.84306A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1441A>G (RAF1)	ENSP00000401088.1:n.*1441A>G
ENST00000432427.3:c.1093A>G (RAF1)
ENST00000460610.2:n.6088A>G (RAF1)
ENST00000471449.2:n.586A>G (RAF1)
ENST00000475353.2:n.4056A>G (RAF1)
ENST00000684903.1:c.*1453A>G (RAF1)	ENSP00000508612.1:n.*1453A>G
ENST00000685348.1:c.*1487A>G (RAF1)	ENSP00000510285.1:n.*1487A>G
ENST00000685437.1:c.1677A>G (RAF1)	ENSP00000508794.1:p.Val559=
ENST00000685653.1:c.1776A>G (RAF1)	ENSP00000509968.1:p.Val592=
ENST00000685697.1:n.2511A>G (RAF1)
ENST00000685738.1:c.*740A>G (RAF1)	ENSP00000510156.1:n.*740A>G
ENST00000686409.1:n.5185A>G (RAF1)
ENST00000686455.1:n.4497A>G (RAF1)
ENST00000686762.1:c.*335A>G (RAF1)	ENSP00000509767.1:n.*335A>G
ENST00000687257.1:n.4230A>G (RAF1)
ENST00000687326.1:c.*3068A>G (RAF1)	ENSP00000509665.1:n.*3068A>G
ENST00000687505.1:n.1894A>G (RAF1)
ENST00000687923.1:c.1665A>G (RAF1)	ENSP00000510255.1:p.Val555=
ENST00000688269.1:n.2372A>G (RAF1)
ENST00000688444.1:n.3893A>G (RAF1)
ENST00000688543.1:c.1677A>G (RAF1)	ENSP00000509612.1:p.Val559=
ENST00000688625.1:c.*3145A>G (RAF1)	ENSP00000509522.1:n.*3145A>G
ENST00000688803.1:n.3204A>G (RAF1)
ENST00000689097.1:c.*1453A>G (RAF1)	ENSP00000509756.1:n.*1453A>G
ENST00000689389.1:c.1599A>G (RAF1)	ENSP00000510213.1:p.Val533=
ENST00000689418.1:c.*3671A>G (RAF1)	ENSP00000509467.1:n.*3671A>G
ENST00000689540.1:n.4144A>G (RAF1)
ENST00000689876.1:c.*325A>G (RAF1)	ENSP00000508535.1:n.*325A>G
ENST00000689914.1:c.*710A>G (RAF1)	ENSP00000509847.1:n.*710A>G
ENST00000690397.1:c.1665A>G (RAF1)	ENSP00000508730.1:p.Val555=
ENST00000690460.1:c.1764A>G (RAF1)	ENSP00000509106.1:p.Val588=
ENST00000690585.1:c.502A>G (RAF1)
ENST00000690625.1:n.2812A>G (RAF1)
ENST00000691396.1:c.*1648A>G (RAF1)	ENSP00000510712.1:n.*1648A>G
ENST00000691643.1:n.2829A>G (RAF1)
ENST00000691724.1:c.*733A>G (RAF1)	ENSP00000509255.1:n.*733A>G
ENST00000691779.1:c.*1354A>G (RAF1)	ENSP00000508592.1:n.*1354A>G
ENST00000691888.1:c.650A>G (RAF1)
ENST00000691899.1:c.1776A>G (RAF1)	ENSP00000508763.1:p.Val592=
ENST00000692069.1:n.4700A>G (RAF1)
ENST00000692093.1:c.1677A>G (RAF1)	ENSP00000509669.1:p.Val559=
ENST00000692311.1:n.2600A>G (RAF1)
ENST00000692558.1:n.4359A>G (RAF1)
ENST00000692773.1:c.*1513A>G (RAF1)	ENSP00000509055.1:n.*1513A>G
ENST00000692830.1:c.*1521A>G (RAF1)	ENSP00000509461.1:n.*1521A>G
ENST00000693312.1:c.1551A>G (RAF1)	ENSP00000508686.1:p.Val517=
ENST00000693664.1:c.*227A>G (RAF1)	ENSP00000509614.1:n.*227A>G
ENST00000693705.1:c.*1155A>G (RAF1)	ENSP00000510697.1:n.*1155A>G
ENST00000251849.9:c.1776A>G (RAF1) MANE Select	ENSP00000251849.4:p.Val592=
ENST00000442415.7:c.1836A>G (RAF1)	ENSP00000401888.2:p.Val612=
ENST00000676541.1:c.*2621T>C (MKRN2)	ENSP00000503730.1:n.*2621T>C
ENST00000677142.1:c.*2621T>C (MKRN2)	ENSP00000504455.1:n.*2621T>C
ENST00000677816.1:c.*1176T>C (MKRN2)	ENSP00000502893.1:n.*1176T>C
ENST00000677941.1:n.2684T>C (MKRN2)
ENST00000251849.8:c.1776A>G (RAF1)	ENSP00000251849.4:p.Val592=
ENST00000423275.5:c.*1453A>G (RAF1)	ENSP00000401088.1:n.*1453A>G
ENST00000432427.2:c.1413A>G (RAF1)	ENSP00000398591.2:p.Val471=
ENST00000442415.6:c.1836A>G (RAF1)	ENSP00000401888.2:p.Val612=
ENST00000471449.1:n.465A>G (RAF1)
NM_002880.3:c.1776A>G , LRG_413t1:c.1776A>G (RAF1)	NP_002871.1:p.Val592=
XM_005265355.1:c.1776A>G (RAF1)	XP_005265412.1:p.Val592=
XM_005265357.1:c.1677A>G (RAF1)	XP_005265414.1:p.Val559=
XM_005265358.3:c.1533A>G (RAF1)	XP_005265415.1:p.Val511=
XM_005265359.3:c.1434A>G (RAF1)	XP_005265416.1:p.Val478=
XM_011533974.1:c.1776A>G (RAF1)	XP_011532276.1:p.Val592=
XM_011533975.1:c.1533A>G (RAF1)	XP_011532277.1:p.Val511=
NM_001354689.1:c.1836A>G (RAF1)	NP_001341618.1:p.Val612=
NM_001354690.1:c.1776A>G (RAF1)	NP_001341619.1:p.Val592=
NM_001354691.1:c.1533A>G (RAF1)	NP_001341620.1:p.Val511=
NM_001354692.1:c.1533A>G (RAF1)	NP_001341621.1:p.Val511=
NM_001354693.1:c.1677A>G (RAF1)	NP_001341622.1:p.Val559=
NM_001354694.1:c.1593A>G (RAF1)	NP_001341623.1:p.Val531=
NM_001354695.1:c.1434A>G (RAF1)	NP_001341624.1:p.Val478=
NR_148940.1:n.2304A>G (RAF1)
NR_148941.1:n.2250A>G (RAF1)
NR_148942.1:n.2189A>G (RAF1)
XM_011533974.3:c.1776A>G (RAF1)	XP_011532276.1:p.Val592=
XM_017006966.1:c.1677A>G (RAF1)	XP_016862455.1:p.Val559=
NM_001354689.3:c.1836A>G (RAF1)	NP_001341618.1:p.Val612=
NM_001354690.2:c.1776A>G (RAF1)	NP_001341619.1:p.Val592=
NM_001354691.2:c.1533A>G (RAF1)	NP_001341620.1:p.Val511=
NM_001354692.2:c.1533A>G (RAF1)	NP_001341621.1:p.Val511=
NM_001354693.2:c.1677A>G (RAF1)	NP_001341622.1:p.Val559=
NM_001354694.2:c.1593A>G (RAF1)	NP_001341623.1:p.Val531=
NM_001354695.2:c.1434A>G (RAF1)	NP_001341624.1:p.Val478=
NR_148940.2:n.2220A>G (RAF1)
NR_148941.2:n.2166A>G (RAF1)
NR_148942.2:n.2105A>G (RAF1)
NM_001354690.3:c.1776A>G (RAF1)	NP_001341619.1:p.Val592=
NM_001354691.3:c.1533A>G (RAF1)	NP_001341620.1:p.Val511=
NM_001354692.3:c.1533A>G (RAF1)	NP_001341621.1:p.Val511=
NM_001354693.3:c.1677A>G (RAF1)	NP_001341622.1:p.Val559=
NM_001354694.3:c.1593A>G (RAF1)	NP_001341623.1:p.Val531=
NM_001354695.3:c.1434A>G (RAF1)	NP_001341624.1:p.Val478=
NM_002880.4:c.1776A>G (RAF1) MANE Select	NP_002871.1:p.Val592=
NR_148940.3:n.2220A>G (RAF1)
NR_148941.3:n.2166A>G (RAF1)
NR_148942.3:n.2105A>G (RAF1)