Canonical Allele Identifier: CA432522064

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626466C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584967C>G , CM000665.2:g.12584967C>G	GRCh38
NC_000003.11:g.12626466C>G , CM000665.1:g.12626466C>G	GRCh37
NC_000003.10:g.12601466C>G	NCBI36
NG_007467.1:g.84213G>C , LRG_413:g.84213G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1348G>C (RAF1)	ENSP00000401088.1:n.*1348G>C
ENST00000432427.3:c.1000G>C (RAF1)
ENST00000460610.2:n.5995G>C (RAF1)
ENST00000471449.2:n.493G>C (RAF1)
ENST00000475353.2:n.3963G>C (RAF1)
ENST00000684903.1:c.*1360G>C (RAF1)	ENSP00000508612.1:n.*1360G>C
ENST00000685348.1:c.*1394G>C (RAF1)	ENSP00000510285.1:n.*1394G>C
ENST00000685437.1:c.1584G>C (RAF1)	ENSP00000508794.1:p.Val528=
ENST00000685653.1:c.1683G>C (RAF1)	ENSP00000509968.1:p.Val561=
ENST00000685697.1:n.2418G>C (RAF1)
ENST00000685738.1:c.*647G>C (RAF1)	ENSP00000510156.1:n.*647G>C
ENST00000686409.1:n.5092G>C (RAF1)
ENST00000686455.1:n.4404G>C (RAF1)
ENST00000686762.1:c.*242G>C (RAF1)	ENSP00000509767.1:n.*242G>C
ENST00000687257.1:n.4137G>C (RAF1)
ENST00000687326.1:c.*2975G>C (RAF1)	ENSP00000509665.1:n.*2975G>C
ENST00000687505.1:n.1801G>C (RAF1)
ENST00000687923.1:c.1572G>C (RAF1)	ENSP00000510255.1:p.Val524=
ENST00000688269.1:n.2279G>C (RAF1)
ENST00000688444.1:n.3800G>C (RAF1)
ENST00000688543.1:c.1584G>C (RAF1)	ENSP00000509612.1:p.Val528=
ENST00000688625.1:c.*3052G>C (RAF1)	ENSP00000509522.1:n.*3052G>C
ENST00000688803.1:n.3111G>C (RAF1)
ENST00000688914.1:n.1096G>C (RAF1)
ENST00000689097.1:c.*1360G>C (RAF1)	ENSP00000509756.1:n.*1360G>C
ENST00000689389.1:c.1506G>C (RAF1)	ENSP00000510213.1:p.Val502=
ENST00000689418.1:c.*3578G>C (RAF1)	ENSP00000509467.1:n.*3578G>C
ENST00000689540.1:n.4051G>C (RAF1)
ENST00000689876.1:c.*232G>C (RAF1)	ENSP00000508535.1:n.*232G>C
ENST00000689914.1:c.*617G>C (RAF1)	ENSP00000509847.1:n.*617G>C
ENST00000690397.1:c.1572G>C (RAF1)	ENSP00000508730.1:p.Val524=
ENST00000690460.1:c.1671G>C (RAF1)	ENSP00000509106.1:p.Val557=
ENST00000690585.1:c.409G>C (RAF1)
ENST00000690625.1:n.2719G>C (RAF1)
ENST00000691396.1:c.*1555G>C (RAF1)	ENSP00000510712.1:n.*1555G>C
ENST00000691643.1:n.2736G>C (RAF1)
ENST00000691724.1:c.*640G>C (RAF1)	ENSP00000509255.1:n.*640G>C
ENST00000691779.1:c.*1261G>C (RAF1)	ENSP00000508592.1:n.*1261G>C
ENST00000691888.1:c.557G>C (RAF1)
ENST00000691899.1:c.1683G>C (RAF1)	ENSP00000508763.1:p.Val561=
ENST00000692069.1:n.4607G>C (RAF1)
ENST00000692093.1:c.1584G>C (RAF1)	ENSP00000509669.1:p.Val528=
ENST00000692311.1:n.2507G>C (RAF1)
ENST00000692558.1:n.4266G>C (RAF1)
ENST00000692773.1:c.*1420G>C (RAF1)	ENSP00000509055.1:n.*1420G>C
ENST00000692830.1:c.*1428G>C (RAF1)	ENSP00000509461.1:n.*1428G>C
ENST00000693312.1:c.1458G>C (RAF1)	ENSP00000508686.1:p.Val486=
ENST00000693664.1:c.*134G>C (RAF1)	ENSP00000509614.1:n.*134G>C
ENST00000693705.1:c.*1062G>C (RAF1)	ENSP00000510697.1:n.*1062G>C
ENST00000251849.9:c.1683G>C (RAF1) MANE Select	ENSP00000251849.4:p.Val561=
ENST00000442415.7:c.1743G>C (RAF1)	ENSP00000401888.2:p.Val581=
ENST00000676541.1:c.*2714C>G (MKRN2)	ENSP00000503730.1:n.*2714C>G
ENST00000677142.1:c.*2714C>G (MKRN2)	ENSP00000504455.1:n.*2714C>G
ENST00000677816.1:c.*1269C>G (MKRN2)	ENSP00000502893.1:n.*1269C>G
ENST00000677941.1:n.2777C>G (MKRN2)
ENST00000251849.8:c.1683G>C (RAF1)	ENSP00000251849.4:p.Val561=
ENST00000423275.5:c.*1360G>C (RAF1)	ENSP00000401088.1:n.*1360G>C
ENST00000432427.2:c.1320G>C (RAF1)	ENSP00000398591.2:p.Val440=
ENST00000442415.6:c.1743G>C (RAF1)	ENSP00000401888.2:p.Val581=
ENST00000471449.1:n.372G>C (RAF1)
NM_002880.3:c.1683G>C , LRG_413t1:c.1683G>C (RAF1)	NP_002871.1:p.Val561=
XM_005265355.1:c.1683G>C (RAF1)	XP_005265412.1:p.Val561=
XM_005265357.1:c.1584G>C (RAF1)	XP_005265414.1:p.Val528=
XM_005265358.3:c.1440G>C (RAF1)	XP_005265415.1:p.Val480=
XM_005265359.3:c.1341G>C (RAF1)	XP_005265416.1:p.Val447=
XM_011533974.1:c.1683G>C (RAF1)	XP_011532276.1:p.Val561=
XM_011533975.1:c.1440G>C (RAF1)	XP_011532277.1:p.Val480=
NM_001354689.1:c.1743G>C (RAF1)	NP_001341618.1:p.Val581=
NM_001354690.1:c.1683G>C (RAF1)	NP_001341619.1:p.Val561=
NM_001354691.1:c.1440G>C (RAF1)	NP_001341620.1:p.Val480=
NM_001354692.1:c.1440G>C (RAF1)	NP_001341621.1:p.Val480=
NM_001354693.1:c.1584G>C (RAF1)	NP_001341622.1:p.Val528=
NM_001354694.1:c.1500G>C (RAF1)	NP_001341623.1:p.Val500=
NM_001354695.1:c.1341G>C (RAF1)	NP_001341624.1:p.Val447=
NR_148940.1:n.2211G>C (RAF1)
NR_148941.1:n.2157G>C (RAF1)
NR_148942.1:n.2096G>C (RAF1)
XM_011533974.3:c.1683G>C (RAF1)	XP_011532276.1:p.Val561=
XM_017006966.1:c.1584G>C (RAF1)	XP_016862455.1:p.Val528=
NM_001354689.3:c.1743G>C (RAF1)	NP_001341618.1:p.Val581=
NM_001354690.2:c.1683G>C (RAF1)	NP_001341619.1:p.Val561=
NM_001354691.2:c.1440G>C (RAF1)	NP_001341620.1:p.Val480=
NM_001354692.2:c.1440G>C (RAF1)	NP_001341621.1:p.Val480=
NM_001354693.2:c.1584G>C (RAF1)	NP_001341622.1:p.Val528=
NM_001354694.2:c.1500G>C (RAF1)	NP_001341623.1:p.Val500=
NM_001354695.2:c.1341G>C (RAF1)	NP_001341624.1:p.Val447=
NR_148940.2:n.2127G>C (RAF1)
NR_148941.2:n.2073G>C (RAF1)
NR_148942.2:n.2012G>C (RAF1)
NM_001354690.3:c.1683G>C (RAF1)	NP_001341619.1:p.Val561=
NM_001354691.3:c.1440G>C (RAF1)	NP_001341620.1:p.Val480=
NM_001354692.3:c.1440G>C (RAF1)	NP_001341621.1:p.Val480=
NM_001354693.3:c.1584G>C (RAF1)	NP_001341622.1:p.Val528=
NM_001354694.3:c.1500G>C (RAF1)	NP_001341623.1:p.Val500=
NM_001354695.3:c.1341G>C (RAF1)	NP_001341624.1:p.Val447=
NM_002880.4:c.1683G>C (RAF1) MANE Select	NP_002871.1:p.Val561=
NR_148940.3:n.2127G>C (RAF1)
NR_148941.3:n.2073G>C (RAF1)
NR_148942.3:n.2012G>C (RAF1)