Canonical Allele Identifier: CA432272833

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs2125325878
• MyVariant Identifiers: chr3:g.12627222A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585723A>C , CM000665.2:g.12585723A>C	GRCh38
NC_000003.11:g.12627222A>C , CM000665.1:g.12627222A>C	GRCh37
NC_000003.10:g.12602222A>C	NCBI36
NG_007467.1:g.83457T>G , LRG_413:g.83457T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1159T>G (RAF1)	ENSP00000401088.1:n.*1159T>G
ENST00000432427.3:c.811T>G (RAF1)
ENST00000460610.2:n.5239T>G (RAF1)
ENST00000471449.2:n.304T>G (RAF1)
ENST00000475353.2:n.3207T>G (RAF1)
ENST00000684903.1:c.*1171T>G (RAF1)	ENSP00000508612.1:n.*1171T>G
ENST00000685348.1:c.*1095-317T>G (RAF1)	ENSP00000510285.1:n.*1095-317T>G
ENST00000685437.1:c.1395T>G (RAF1)	ENSP00000508794.1:p.Gly465=
ENST00000685653.1:c.1494T>G (RAF1)	ENSP00000509968.1:p.Gly498=
ENST00000685697.1:n.2229T>G (RAF1)
ENST00000685738.1:c.*458T>G (RAF1)	ENSP00000510156.1:n.*458T>G
ENST00000686409.1:n.4336T>G (RAF1)
ENST00000686455.1:n.3648T>G (RAF1)
ENST00000686762.1:c.*53T>G (RAF1)	ENSP00000509767.1:n.*53T>G
ENST00000687257.1:n.3521T>G (RAF1)
ENST00000687326.1:c.*2219T>G (RAF1)	ENSP00000509665.1:n.*2219T>G
ENST00000687505.1:n.1612T>G (RAF1)
ENST00000687923.1:c.1383T>G (RAF1)	ENSP00000510255.1:p.Gly461=
ENST00000688269.1:n.2090T>G (RAF1)
ENST00000688444.1:n.3611T>G (RAF1)
ENST00000688543.1:c.1395T>G (RAF1)	ENSP00000509612.1:p.Gly465=
ENST00000688625.1:c.*2863T>G (RAF1)	ENSP00000509522.1:n.*2863T>G
ENST00000688803.1:n.2965-470T>G (RAF1)
ENST00000688914.1:n.480T>G (RAF1)
ENST00000689097.1:c.*1171T>G (RAF1)	ENSP00000509756.1:n.*1171T>G
ENST00000689389.1:c.1317T>G (RAF1)	ENSP00000510213.1:p.Gly439=
ENST00000689418.1:c.*2962T>G (RAF1)	ENSP00000509467.1:n.*2962T>G
ENST00000689540.1:n.3435T>G (RAF1)
ENST00000689876.1:c.1418-317T>G (RAF1)	ENSP00000508535.1:n.1418-317T>G
ENST00000689914.1:c.*428T>G (RAF1)	ENSP00000509847.1:n.*428T>G
ENST00000690397.1:c.1383T>G (RAF1)	ENSP00000508730.1:p.Gly461=
ENST00000690460.1:c.1482T>G (RAF1)	ENSP00000509106.1:p.Gly494=
ENST00000690585.1:c.263-470T>G (RAF1)
ENST00000690625.1:n.2530T>G (RAF1)
ENST00000691396.1:c.*1366T>G (RAF1)	ENSP00000510712.1:n.*1366T>G
ENST00000691643.1:n.2120T>G (RAF1)
ENST00000691724.1:c.*451T>G (RAF1)	ENSP00000509255.1:n.*451T>G
ENST00000691779.1:c.*1072T>G (RAF1)	ENSP00000508592.1:n.*1072T>G
ENST00000691888.1:c.368T>G (RAF1)
ENST00000691899.1:c.1494T>G (RAF1)	ENSP00000508763.1:p.Gly498=
ENST00000692069.1:n.3851T>G (RAF1)
ENST00000692093.1:c.1395T>G (RAF1)	ENSP00000509669.1:p.Gly465=
ENST00000692311.1:n.2318T>G (RAF1)
ENST00000692558.1:n.3650T>G (RAF1)
ENST00000692773.1:c.*1231T>G (RAF1)	ENSP00000509055.1:n.*1231T>G
ENST00000692830.1:c.*1239T>G (RAF1)	ENSP00000509461.1:n.*1239T>G
ENST00000693312.1:c.1269T>G (RAF1)	ENSP00000508686.1:p.Gly423=
ENST00000693664.1:c.1488-470T>G (RAF1)	ENSP00000509614.1:n.1488-470T>G
ENST00000693705.1:c.*1048-742T>G (RAF1)	ENSP00000510697.1:n.*1048-742T>G
ENST00000251849.9:c.1494T>G (RAF1) MANE Select	ENSP00000251849.4:p.Gly498=
ENST00000442415.7:c.1554T>G (RAF1)	ENSP00000401888.2:p.Gly518=
ENST00000676541.1:c.*3470A>C (MKRN2)	ENSP00000503730.1:n.*3470A>C
ENST00000677142.1:c.*3470A>C (MKRN2)	ENSP00000504455.1:n.*3470A>C
ENST00000677816.1:c.*2025A>C (MKRN2)	ENSP00000502893.1:n.*2025A>C
ENST00000677941.1:n.3533A>C (MKRN2)
ENST00000251849.8:c.1494T>G (RAF1)	ENSP00000251849.4:p.Gly498=
ENST00000423275.5:c.*1171T>G (RAF1)	ENSP00000401088.1:n.*1171T>G
ENST00000432427.2:c.1131T>G (RAF1)	ENSP00000398591.2:p.Gly377=
ENST00000442415.6:c.1554T>G (RAF1)	ENSP00000401888.2:p.Gly518=
ENST00000471449.1:n.183T>G (RAF1)
NM_002880.3:c.1494T>G , LRG_413t1:c.1494T>G (RAF1)	NP_002871.1:p.Gly498=
XM_005265355.1:c.1494T>G (RAF1)	XP_005265412.1:p.Gly498=
XM_005265357.1:c.1395T>G (RAF1)	XP_005265414.1:p.Gly465=
XM_005265358.3:c.1251T>G (RAF1)	XP_005265415.1:p.Gly417=
XM_005265359.3:c.1152T>G (RAF1)	XP_005265416.1:p.Gly384=
XM_005265360.1:c.1418-317T>G (RAF1)	XP_005265417.1:n.1418-317T>G
XM_011533974.1:c.1494T>G (RAF1)	XP_011532276.1:p.Gly498=
XM_011533975.1:c.1251T>G (RAF1)	XP_011532277.1:p.Gly417=
NM_001354689.1:c.1554T>G (RAF1)	NP_001341618.1:p.Gly518=
NM_001354690.1:c.1494T>G (RAF1)	NP_001341619.1:p.Gly498=
NM_001354691.1:c.1251T>G (RAF1)	NP_001341620.1:p.Gly417=
NM_001354692.1:c.1251T>G (RAF1)	NP_001341621.1:p.Gly417=
NM_001354693.1:c.1395T>G (RAF1)	NP_001341622.1:p.Gly465=
NM_001354694.1:c.1311T>G (RAF1)	NP_001341623.1:p.Gly437=
NM_001354695.1:c.1152T>G (RAF1)	NP_001341624.1:p.Gly384=
NR_148940.1:n.2022T>G (RAF1)
NR_148941.1:n.1968T>G (RAF1)
NR_148942.1:n.1907T>G (RAF1)
XM_011533974.3:c.1494T>G (RAF1)	XP_011532276.1:p.Gly498=
XM_017006966.1:c.1395T>G (RAF1)	XP_016862455.1:p.Gly465=
NM_001354689.3:c.1554T>G (RAF1)	NP_001341618.1:p.Gly518=
NM_001354690.2:c.1494T>G (RAF1)	NP_001341619.1:p.Gly498=
NM_001354691.2:c.1251T>G (RAF1)	NP_001341620.1:p.Gly417=
NM_001354692.2:c.1251T>G (RAF1)	NP_001341621.1:p.Gly417=
NM_001354693.2:c.1395T>G (RAF1)	NP_001341622.1:p.Gly465=
NM_001354694.2:c.1311T>G (RAF1)	NP_001341623.1:p.Gly437=
NM_001354695.2:c.1152T>G (RAF1)	NP_001341624.1:p.Gly384=
NR_148940.2:n.1938T>G (RAF1)
NR_148941.2:n.1884T>G (RAF1)
NR_148942.2:n.1823T>G (RAF1)
NM_001354690.3:c.1494T>G (RAF1)	NP_001341619.1:p.Gly498=
NM_001354691.3:c.1251T>G (RAF1)	NP_001341620.1:p.Gly417=
NM_001354692.3:c.1251T>G (RAF1)	NP_001341621.1:p.Gly417=
NM_001354693.3:c.1395T>G (RAF1)	NP_001341622.1:p.Gly465=
NM_001354694.3:c.1311T>G (RAF1)	NP_001341623.1:p.Gly437=
NM_001354695.3:c.1152T>G (RAF1)	NP_001341624.1:p.Gly384=
NM_002880.4:c.1494T>G (RAF1) MANE Select	NP_002871.1:p.Gly498=
NR_148940.3:n.1938T>G (RAF1)
NR_148941.3:n.1884T>G (RAF1)
NR_148942.3:n.1823T>G (RAF1)