Canonical Allele Identifier: CA432272859

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12627261T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585762T>C , CM000665.2:g.12585762T>C	GRCh38
NC_000003.11:g.12627261T>C , CM000665.1:g.12627261T>C	GRCh37
NC_000003.10:g.12602261T>C	NCBI36
NG_007467.1:g.83418A>G , LRG_413:g.83418A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1120A>G (RAF1)	ENSP00000401088.1:n.*1120A>G
ENST00000432427.3:c.772A>G (RAF1)
ENST00000460610.2:n.5200A>G (RAF1)
ENST00000471449.2:n.265A>G (RAF1)
ENST00000475353.2:n.3168A>G (RAF1)
ENST00000684903.1:c.*1132A>G (RAF1)	ENSP00000508612.1:n.*1132A>G
ENST00000685348.1:c.*1095-356A>G (RAF1)	ENSP00000510285.1:n.*1095-356A>G
ENST00000685437.1:c.1356A>G (RAF1)	ENSP00000508794.1:p.Gly452=
ENST00000685653.1:c.1455A>G (RAF1)	ENSP00000509968.1:p.Gly485=
ENST00000685697.1:n.2190A>G (RAF1)
ENST00000685738.1:c.*419A>G (RAF1)	ENSP00000510156.1:n.*419A>G
ENST00000686409.1:n.4297A>G (RAF1)
ENST00000686455.1:n.3609A>G (RAF1)
ENST00000686762.1:c.*14A>G (RAF1)	ENSP00000509767.1:n.*14A>G
ENST00000687257.1:n.3482A>G (RAF1)
ENST00000687326.1:c.*2180A>G (RAF1)	ENSP00000509665.1:n.*2180A>G
ENST00000687505.1:n.1573A>G (RAF1)
ENST00000687923.1:c.1344A>G (RAF1)	ENSP00000510255.1:p.Gly448=
ENST00000688269.1:n.2051A>G (RAF1)
ENST00000688444.1:n.3572A>G (RAF1)
ENST00000688543.1:c.1356A>G (RAF1)	ENSP00000509612.1:p.Gly452=
ENST00000688625.1:c.*2824A>G (RAF1)	ENSP00000509522.1:n.*2824A>G
ENST00000688803.1:n.2965-509A>G (RAF1)
ENST00000688914.1:n.441A>G (RAF1)
ENST00000689097.1:c.*1132A>G (RAF1)	ENSP00000509756.1:n.*1132A>G
ENST00000689389.1:c.1278A>G (RAF1)	ENSP00000510213.1:p.Gly426=
ENST00000689418.1:c.*2923A>G (RAF1)	ENSP00000509467.1:n.*2923A>G
ENST00000689540.1:n.3396A>G (RAF1)
ENST00000689876.1:c.1418-356A>G (RAF1)	ENSP00000508535.1:n.1418-356A>G
ENST00000689914.1:c.*389A>G (RAF1)	ENSP00000509847.1:n.*389A>G
ENST00000690397.1:c.1344A>G (RAF1)	ENSP00000508730.1:p.Gly448=
ENST00000690460.1:c.1443A>G (RAF1)	ENSP00000509106.1:p.Gly481=
ENST00000690585.1:c.263-509A>G (RAF1)
ENST00000690625.1:n.2491A>G (RAF1)
ENST00000691396.1:c.*1327A>G (RAF1)	ENSP00000510712.1:n.*1327A>G
ENST00000691643.1:n.2081A>G (RAF1)
ENST00000691724.1:c.*412A>G (RAF1)	ENSP00000509255.1:n.*412A>G
ENST00000691779.1:c.*1033A>G (RAF1)	ENSP00000508592.1:n.*1033A>G
ENST00000691888.1:c.329A>G (RAF1)
ENST00000691899.1:c.1455A>G (RAF1)	ENSP00000508763.1:p.Gly485=
ENST00000692069.1:n.3812A>G (RAF1)
ENST00000692093.1:c.1356A>G (RAF1)	ENSP00000509669.1:p.Gly452=
ENST00000692311.1:n.2279A>G (RAF1)
ENST00000692558.1:n.3611A>G (RAF1)
ENST00000692773.1:c.*1192A>G (RAF1)	ENSP00000509055.1:n.*1192A>G
ENST00000692830.1:c.*1200A>G (RAF1)	ENSP00000509461.1:n.*1200A>G
ENST00000693312.1:c.1230A>G (RAF1)	ENSP00000508686.1:p.Gly410=
ENST00000693664.1:c.1488-509A>G (RAF1)	ENSP00000509614.1:n.1488-509A>G
ENST00000693705.1:c.*1048-781A>G (RAF1)	ENSP00000510697.1:n.*1048-781A>G
ENST00000251849.9:c.1455A>G (RAF1) MANE Select	ENSP00000251849.4:p.Gly485=
ENST00000442415.7:c.1515A>G (RAF1)	ENSP00000401888.2:p.Gly505=
ENST00000676541.1:c.*3509T>C (MKRN2)	ENSP00000503730.1:n.*3509T>C
ENST00000677142.1:c.*3509T>C (MKRN2)	ENSP00000504455.1:n.*3509T>C
ENST00000677816.1:c.*2064T>C (MKRN2)	ENSP00000502893.1:n.*2064T>C
ENST00000677941.1:n.3572T>C (MKRN2)
ENST00000251849.8:c.1455A>G (RAF1)	ENSP00000251849.4:p.Gly485=
ENST00000423275.5:c.*1132A>G (RAF1)	ENSP00000401088.1:n.*1132A>G
ENST00000432427.2:c.1092A>G (RAF1)	ENSP00000398591.2:p.Gly364=
ENST00000442415.6:c.1515A>G (RAF1)	ENSP00000401888.2:p.Gly505=
ENST00000471449.1:n.144A>G (RAF1)
NM_002880.3:c.1455A>G , LRG_413t1:c.1455A>G (RAF1)	NP_002871.1:p.Gly485=
XM_005265355.1:c.1455A>G (RAF1)	XP_005265412.1:p.Gly485=
XM_005265357.1:c.1356A>G (RAF1)	XP_005265414.1:p.Gly452=
XM_005265358.3:c.1212A>G (RAF1)	XP_005265415.1:p.Gly404=
XM_005265359.3:c.1113A>G (RAF1)	XP_005265416.1:p.Gly371=
XM_005265360.1:c.1418-356A>G (RAF1)	XP_005265417.1:n.1418-356A>G
XM_011533974.1:c.1455A>G (RAF1)	XP_011532276.1:p.Gly485=
XM_011533975.1:c.1212A>G (RAF1)	XP_011532277.1:p.Gly404=
NM_001354689.1:c.1515A>G (RAF1)	NP_001341618.1:p.Gly505=
NM_001354690.1:c.1455A>G (RAF1)	NP_001341619.1:p.Gly485=
NM_001354691.1:c.1212A>G (RAF1)	NP_001341620.1:p.Gly404=
NM_001354692.1:c.1212A>G (RAF1)	NP_001341621.1:p.Gly404=
NM_001354693.1:c.1356A>G (RAF1)	NP_001341622.1:p.Gly452=
NM_001354694.1:c.1272A>G (RAF1)	NP_001341623.1:p.Gly424=
NM_001354695.1:c.1113A>G (RAF1)	NP_001341624.1:p.Gly371=
NR_148940.1:n.1983A>G (RAF1)
NR_148941.1:n.1929A>G (RAF1)
NR_148942.1:n.1868A>G (RAF1)
XM_011533974.3:c.1455A>G (RAF1)	XP_011532276.1:p.Gly485=
XM_017006966.1:c.1356A>G (RAF1)	XP_016862455.1:p.Gly452=
NM_001354689.3:c.1515A>G (RAF1)	NP_001341618.1:p.Gly505=
NM_001354690.2:c.1455A>G (RAF1)	NP_001341619.1:p.Gly485=
NM_001354691.2:c.1212A>G (RAF1)	NP_001341620.1:p.Gly404=
NM_001354692.2:c.1212A>G (RAF1)	NP_001341621.1:p.Gly404=
NM_001354693.2:c.1356A>G (RAF1)	NP_001341622.1:p.Gly452=
NM_001354694.2:c.1272A>G (RAF1)	NP_001341623.1:p.Gly424=
NM_001354695.2:c.1113A>G (RAF1)	NP_001341624.1:p.Gly371=
NR_148940.2:n.1899A>G (RAF1)
NR_148941.2:n.1845A>G (RAF1)
NR_148942.2:n.1784A>G (RAF1)
NM_001354690.3:c.1455A>G (RAF1)	NP_001341619.1:p.Gly485=
NM_001354691.3:c.1212A>G (RAF1)	NP_001341620.1:p.Gly404=
NM_001354692.3:c.1212A>G (RAF1)	NP_001341621.1:p.Gly404=
NM_001354693.3:c.1356A>G (RAF1)	NP_001341622.1:p.Gly452=
NM_001354694.3:c.1272A>G (RAF1)	NP_001341623.1:p.Gly424=
NM_001354695.3:c.1113A>G (RAF1)	NP_001341624.1:p.Gly371=
NM_002880.4:c.1455A>G (RAF1) MANE Select	NP_002871.1:p.Gly485=
NR_148940.3:n.1899A>G (RAF1)
NR_148941.3:n.1845A>G (RAF1)
NR_148942.3:n.1784A>G (RAF1)