Canonical Allele Identifier: CA432522050

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626448G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584949G>C , CM000665.2:g.12584949G>C	GRCh38
NC_000003.11:g.12626448G>C , CM000665.1:g.12626448G>C	GRCh37
NC_000003.10:g.12601448G>C	NCBI36
NG_007467.1:g.84231C>G , LRG_413:g.84231C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1366C>G (RAF1)	ENSP00000401088.1:n.*1366C>G
ENST00000432427.3:c.1018C>G (RAF1)
ENST00000460610.2:n.6013C>G (RAF1)
ENST00000471449.2:n.511C>G (RAF1)
ENST00000475353.2:n.3981C>G (RAF1)
ENST00000684903.1:c.*1378C>G (RAF1)	ENSP00000508612.1:n.*1378C>G
ENST00000685348.1:c.*1412C>G (RAF1)	ENSP00000510285.1:n.*1412C>G
ENST00000685437.1:c.1602C>G (RAF1)	ENSP00000508794.1:p.Ser534=
ENST00000685653.1:c.1701C>G (RAF1)	ENSP00000509968.1:p.Ser567=
ENST00000685697.1:n.2436C>G (RAF1)
ENST00000685738.1:c.*665C>G (RAF1)	ENSP00000510156.1:n.*665C>G
ENST00000686409.1:n.5110C>G (RAF1)
ENST00000686455.1:n.4422C>G (RAF1)
ENST00000686762.1:c.*260C>G (RAF1)	ENSP00000509767.1:n.*260C>G
ENST00000687257.1:n.4155C>G (RAF1)
ENST00000687326.1:c.*2993C>G (RAF1)	ENSP00000509665.1:n.*2993C>G
ENST00000687505.1:n.1819C>G (RAF1)
ENST00000687923.1:c.1590C>G (RAF1)	ENSP00000510255.1:p.Ser530=
ENST00000688269.1:n.2297C>G (RAF1)
ENST00000688444.1:n.3818C>G (RAF1)
ENST00000688543.1:c.1602C>G (RAF1)	ENSP00000509612.1:p.Ser534=
ENST00000688625.1:c.*3070C>G (RAF1)	ENSP00000509522.1:n.*3070C>G
ENST00000688803.1:n.3129C>G (RAF1)
ENST00000688914.1:n.1114C>G (RAF1)
ENST00000689097.1:c.*1378C>G (RAF1)	ENSP00000509756.1:n.*1378C>G
ENST00000689389.1:c.1524C>G (RAF1)	ENSP00000510213.1:p.Ser508=
ENST00000689418.1:c.*3596C>G (RAF1)	ENSP00000509467.1:n.*3596C>G
ENST00000689540.1:n.4069C>G (RAF1)
ENST00000689876.1:c.*250C>G (RAF1)	ENSP00000508535.1:n.*250C>G
ENST00000689914.1:c.*635C>G (RAF1)	ENSP00000509847.1:n.*635C>G
ENST00000690397.1:c.1590C>G (RAF1)	ENSP00000508730.1:p.Ser530=
ENST00000690460.1:c.1689C>G (RAF1)	ENSP00000509106.1:p.Ser563=
ENST00000690585.1:c.427C>G (RAF1)
ENST00000690625.1:n.2737C>G (RAF1)
ENST00000691396.1:c.*1573C>G (RAF1)	ENSP00000510712.1:n.*1573C>G
ENST00000691643.1:n.2754C>G (RAF1)
ENST00000691724.1:c.*658C>G (RAF1)	ENSP00000509255.1:n.*658C>G
ENST00000691779.1:c.*1279C>G (RAF1)	ENSP00000508592.1:n.*1279C>G
ENST00000691888.1:c.575C>G (RAF1)
ENST00000691899.1:c.1701C>G (RAF1)	ENSP00000508763.1:p.Ser567=
ENST00000692069.1:n.4625C>G (RAF1)
ENST00000692093.1:c.1602C>G (RAF1)	ENSP00000509669.1:p.Ser534=
ENST00000692311.1:n.2525C>G (RAF1)
ENST00000692558.1:n.4284C>G (RAF1)
ENST00000692773.1:c.*1438C>G (RAF1)	ENSP00000509055.1:n.*1438C>G
ENST00000692830.1:c.*1446C>G (RAF1)	ENSP00000509461.1:n.*1446C>G
ENST00000693312.1:c.1476C>G (RAF1)	ENSP00000508686.1:p.Ser492=
ENST00000693664.1:c.*152C>G (RAF1)	ENSP00000509614.1:n.*152C>G
ENST00000693705.1:c.*1080C>G (RAF1)	ENSP00000510697.1:n.*1080C>G
ENST00000251849.9:c.1701C>G (RAF1) MANE Select	ENSP00000251849.4:p.Ser567=
ENST00000442415.7:c.1761C>G (RAF1)	ENSP00000401888.2:p.Ser587=
ENST00000676541.1:c.*2696G>C (MKRN2)	ENSP00000503730.1:n.*2696G>C
ENST00000677142.1:c.*2696G>C (MKRN2)	ENSP00000504455.1:n.*2696G>C
ENST00000677816.1:c.*1251G>C (MKRN2)	ENSP00000502893.1:n.*1251G>C
ENST00000677941.1:n.2759G>C (MKRN2)
ENST00000251849.8:c.1701C>G (RAF1)	ENSP00000251849.4:p.Ser567=
ENST00000423275.5:c.*1378C>G (RAF1)	ENSP00000401088.1:n.*1378C>G
ENST00000432427.2:c.1338C>G (RAF1)	ENSP00000398591.2:p.Ser446=
ENST00000442415.6:c.1761C>G (RAF1)	ENSP00000401888.2:p.Ser587=
ENST00000471449.1:n.390C>G (RAF1)
NM_002880.3:c.1701C>G , LRG_413t1:c.1701C>G (RAF1)	NP_002871.1:p.Ser567=
XM_005265355.1:c.1701C>G (RAF1)	XP_005265412.1:p.Ser567=
XM_005265357.1:c.1602C>G (RAF1)	XP_005265414.1:p.Ser534=
XM_005265358.3:c.1458C>G (RAF1)	XP_005265415.1:p.Ser486=
XM_005265359.3:c.1359C>G (RAF1)	XP_005265416.1:p.Ser453=
XM_011533974.1:c.1701C>G (RAF1)	XP_011532276.1:p.Ser567=
XM_011533975.1:c.1458C>G (RAF1)	XP_011532277.1:p.Ser486=
NM_001354689.1:c.1761C>G (RAF1)	NP_001341618.1:p.Ser587=
NM_001354690.1:c.1701C>G (RAF1)	NP_001341619.1:p.Ser567=
NM_001354691.1:c.1458C>G (RAF1)	NP_001341620.1:p.Ser486=
NM_001354692.1:c.1458C>G (RAF1)	NP_001341621.1:p.Ser486=
NM_001354693.1:c.1602C>G (RAF1)	NP_001341622.1:p.Ser534=
NM_001354694.1:c.1518C>G (RAF1)	NP_001341623.1:p.Ser506=
NM_001354695.1:c.1359C>G (RAF1)	NP_001341624.1:p.Ser453=
NR_148940.1:n.2229C>G (RAF1)
NR_148941.1:n.2175C>G (RAF1)
NR_148942.1:n.2114C>G (RAF1)
XM_011533974.3:c.1701C>G (RAF1)	XP_011532276.1:p.Ser567=
XM_017006966.1:c.1602C>G (RAF1)	XP_016862455.1:p.Ser534=
NM_001354689.3:c.1761C>G (RAF1)	NP_001341618.1:p.Ser587=
NM_001354690.2:c.1701C>G (RAF1)	NP_001341619.1:p.Ser567=
NM_001354691.2:c.1458C>G (RAF1)	NP_001341620.1:p.Ser486=
NM_001354692.2:c.1458C>G (RAF1)	NP_001341621.1:p.Ser486=
NM_001354693.2:c.1602C>G (RAF1)	NP_001341622.1:p.Ser534=
NM_001354694.2:c.1518C>G (RAF1)	NP_001341623.1:p.Ser506=
NM_001354695.2:c.1359C>G (RAF1)	NP_001341624.1:p.Ser453=
NR_148940.2:n.2145C>G (RAF1)
NR_148941.2:n.2091C>G (RAF1)
NR_148942.2:n.2030C>G (RAF1)
NM_001354690.3:c.1701C>G (RAF1)	NP_001341619.1:p.Ser567=
NM_001354691.3:c.1458C>G (RAF1)	NP_001341620.1:p.Ser486=
NM_001354692.3:c.1458C>G (RAF1)	NP_001341621.1:p.Ser486=
NM_001354693.3:c.1602C>G (RAF1)	NP_001341622.1:p.Ser534=
NM_001354694.3:c.1518C>G (RAF1)	NP_001341623.1:p.Ser506=
NM_001354695.3:c.1359C>G (RAF1)	NP_001341624.1:p.Ser453=
NM_002880.4:c.1701C>G (RAF1) MANE Select	NP_002871.1:p.Ser567=
NR_148940.3:n.2145C>G (RAF1)
NR_148941.3:n.2091C>G (RAF1)
NR_148942.3:n.2030C>G (RAF1)