Canonical Allele Identifier: CA351499162

Gene: RAF1 MKRN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585761C>G , CM000665.2:g.12585761C>G	GRCh38
NC_000003.11:g.12627260C>G , CM000665.1:g.12627260C>G	GRCh37
NC_000003.10:g.12602260C>G	NCBI36
NG_007467.1:g.83419G>C , LRG_413:g.83419G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1121G>C (RAF1)	ENSP00000401088.1:n.*1121G>C
ENST00000432427.3:c.773G>C (RAF1)
ENST00000460610.2:n.5201G>C (RAF1)
ENST00000471449.2:n.266G>C (RAF1)
ENST00000475353.2:n.3169G>C (RAF1)
ENST00000684903.1:c.*1133G>C (RAF1)	ENSP00000508612.1:n.*1133G>C
ENST00000685348.1:c.*1095-355G>C (RAF1)	ENSP00000510285.1:n.*1095-355G>C
ENST00000685437.1:c.1357G>C (RAF1)	ENSP00000508794.1:p.Asp453His
ENST00000685653.1:c.1456G>C (RAF1)	ENSP00000509968.1:p.Asp486His
ENST00000685697.1:n.2191G>C (RAF1)
ENST00000685738.1:c.*420G>C (RAF1)	ENSP00000510156.1:n.*420G>C
ENST00000686409.1:n.4298G>C (RAF1)
ENST00000686455.1:n.3610G>C (RAF1)
ENST00000686762.1:c.*15G>C (RAF1)	ENSP00000509767.1:n.*15G>C
ENST00000687257.1:n.3483G>C (RAF1)
ENST00000687326.1:c.*2181G>C (RAF1)	ENSP00000509665.1:n.*2181G>C
ENST00000687505.1:n.1574G>C (RAF1)
ENST00000687923.1:c.1345G>C (RAF1)	ENSP00000510255.1:p.Asp449His
ENST00000688269.1:n.2052G>C (RAF1)
ENST00000688444.1:n.3573G>C (RAF1)
ENST00000688543.1:c.1357G>C (RAF1)	ENSP00000509612.1:p.Asp453His
ENST00000688625.1:c.*2825G>C (RAF1)	ENSP00000509522.1:n.*2825G>C
ENST00000688803.1:n.2965-508G>C (RAF1)
ENST00000688914.1:n.442G>C (RAF1)
ENST00000689097.1:c.*1133G>C (RAF1)	ENSP00000509756.1:n.*1133G>C
ENST00000689389.1:c.1279G>C (RAF1)	ENSP00000510213.1:p.Asp427His
ENST00000689418.1:c.*2924G>C (RAF1)	ENSP00000509467.1:n.*2924G>C
ENST00000689540.1:n.3397G>C (RAF1)
ENST00000689876.1:c.1418-355G>C (RAF1)	ENSP00000508535.1:n.1418-355G>C
ENST00000689914.1:c.*390G>C (RAF1)	ENSP00000509847.1:n.*390G>C
ENST00000690397.1:c.1345G>C (RAF1)	ENSP00000508730.1:p.Asp449His
ENST00000690460.1:c.1444G>C (RAF1)	ENSP00000509106.1:p.Asp482His
ENST00000690585.1:c.263-508G>C (RAF1)
ENST00000690625.1:n.2492G>C (RAF1)
ENST00000691396.1:c.*1328G>C (RAF1)	ENSP00000510712.1:n.*1328G>C
ENST00000691643.1:n.2082G>C (RAF1)
ENST00000691724.1:c.*413G>C (RAF1)	ENSP00000509255.1:n.*413G>C
ENST00000691779.1:c.*1034G>C (RAF1)	ENSP00000508592.1:n.*1034G>C
ENST00000691888.1:c.330G>C (RAF1)
ENST00000691899.1:c.1456G>C (RAF1)	ENSP00000508763.1:p.Asp486His
ENST00000692069.1:n.3813G>C (RAF1)
ENST00000692093.1:c.1357G>C (RAF1)	ENSP00000509669.1:p.Asp453His
ENST00000692311.1:n.2280G>C (RAF1)
ENST00000692558.1:n.3612G>C (RAF1)
ENST00000692773.1:c.*1193G>C (RAF1)	ENSP00000509055.1:n.*1193G>C
ENST00000692830.1:c.*1201G>C (RAF1)	ENSP00000509461.1:n.*1201G>C
ENST00000693312.1:c.1231G>C (RAF1)	ENSP00000508686.1:p.Asp411His
ENST00000693664.1:c.1488-508G>C (RAF1)	ENSP00000509614.1:n.1488-508G>C
ENST00000693705.1:c.*1048-780G>C (RAF1)	ENSP00000510697.1:n.*1048-780G>C
ENST00000251849.9:c.1456G>C (RAF1) MANE Select	ENSP00000251849.4:p.Asp486His
ENST00000442415.7:c.1516G>C (RAF1)	ENSP00000401888.2:p.Asp506His
ENST00000676541.1:c.*3508C>G (MKRN2)	ENSP00000503730.1:n.*3508C>G
ENST00000677142.1:c.*3508C>G (MKRN2)	ENSP00000504455.1:n.*3508C>G
ENST00000677816.1:c.*2063C>G (MKRN2)	ENSP00000502893.1:n.*2063C>G
ENST00000677941.1:n.3571C>G (MKRN2)
ENST00000251849.8:c.1456G>C (RAF1)	ENSP00000251849.4:p.Asp486His
ENST00000423275.5:c.*1133G>C (RAF1)	ENSP00000401088.1:n.*1133G>C
ENST00000432427.2:c.1093G>C (RAF1)	ENSP00000398591.2:p.Asp365His
ENST00000442415.6:c.1516G>C (RAF1)	ENSP00000401888.2:p.Asp506His
ENST00000471449.1:n.145G>C (RAF1)
NM_002880.3:c.1456G>C , LRG_413t1:c.1456G>C (RAF1)	NP_002871.1:p.Asp486His
XM_005265355.1:c.1456G>C (RAF1)	XP_005265412.1:p.Asp486His
XM_005265357.1:c.1357G>C (RAF1)	XP_005265414.1:p.Asp453His
XM_005265358.3:c.1213G>C (RAF1)	XP_005265415.1:p.Asp405His
XM_005265359.3:c.1114G>C (RAF1)	XP_005265416.1:p.Asp372His
XM_005265360.1:c.1418-355G>C (RAF1)	XP_005265417.1:n.1418-355G>C
XM_011533974.1:c.1456G>C (RAF1)	XP_011532276.1:p.Asp486His
XM_011533975.1:c.1213G>C (RAF1)	XP_011532277.1:p.Asp405His
NM_001354689.1:c.1516G>C (RAF1)	NP_001341618.1:p.Asp506His
NM_001354690.1:c.1456G>C (RAF1)	NP_001341619.1:p.Asp486His
NM_001354691.1:c.1213G>C (RAF1)	NP_001341620.1:p.Asp405His
NM_001354692.1:c.1213G>C (RAF1)	NP_001341621.1:p.Asp405His
NM_001354693.1:c.1357G>C (RAF1)	NP_001341622.1:p.Asp453His
NM_001354694.1:c.1273G>C (RAF1)	NP_001341623.1:p.Asp425His
NM_001354695.1:c.1114G>C (RAF1)	NP_001341624.1:p.Asp372His
NR_148940.1:n.1984G>C (RAF1)
NR_148941.1:n.1930G>C (RAF1)
NR_148942.1:n.1869G>C (RAF1)
XM_011533974.3:c.1456G>C (RAF1)	XP_011532276.1:p.Asp486His
XM_017006966.1:c.1357G>C (RAF1)	XP_016862455.1:p.Asp453His
NM_001354689.3:c.1516G>C (RAF1)	NP_001341618.1:p.Asp506His
NM_001354690.2:c.1456G>C (RAF1)	NP_001341619.1:p.Asp486His
NM_001354691.2:c.1213G>C (RAF1)	NP_001341620.1:p.Asp405His
NM_001354692.2:c.1213G>C (RAF1)	NP_001341621.1:p.Asp405His
NM_001354693.2:c.1357G>C (RAF1)	NP_001341622.1:p.Asp453His
NM_001354694.2:c.1273G>C (RAF1)	NP_001341623.1:p.Asp425His
NM_001354695.2:c.1114G>C (RAF1)	NP_001341624.1:p.Asp372His
NR_148940.2:n.1900G>C (RAF1)
NR_148941.2:n.1846G>C (RAF1)
NR_148942.2:n.1785G>C (RAF1)
NM_001354690.3:c.1456G>C (RAF1)	NP_001341619.1:p.Asp486His
NM_001354691.3:c.1213G>C (RAF1)	NP_001341620.1:p.Asp405His
NM_001354692.3:c.1213G>C (RAF1)	NP_001341621.1:p.Asp405His
NM_001354693.3:c.1357G>C (RAF1)	NP_001341622.1:p.Asp453His
NM_001354694.3:c.1273G>C (RAF1)	NP_001341623.1:p.Asp425His
NM_001354695.3:c.1114G>C (RAF1)	NP_001341624.1:p.Asp372His
NM_002880.4:c.1456G>C (RAF1) MANE Select	NP_002871.1:p.Asp486His
NR_148940.3:n.1900G>C (RAF1)
NR_148941.3:n.1846G>C (RAF1)
NR_148942.3:n.1785G>C (RAF1)