Canonical Allele Identifier: CA432522015

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626391A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584892A>C , CM000665.2:g.12584892A>C	GRCh38
NC_000003.11:g.12626391A>C , CM000665.1:g.12626391A>C	GRCh37
NC_000003.10:g.12601391A>C	NCBI36
NG_007467.1:g.84288T>G , LRG_413:g.84288T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1423T>G (RAF1)	ENSP00000401088.1:n.*1423T>G
ENST00000432427.3:c.1075T>G (RAF1)
ENST00000460610.2:n.6070T>G (RAF1)
ENST00000471449.2:n.568T>G (RAF1)
ENST00000475353.2:n.4038T>G (RAF1)
ENST00000684903.1:c.*1435T>G (RAF1)	ENSP00000508612.1:n.*1435T>G
ENST00000685348.1:c.*1469T>G (RAF1)	ENSP00000510285.1:n.*1469T>G
ENST00000685437.1:c.1659T>G (RAF1)	ENSP00000508794.1:p.Ala553=
ENST00000685653.1:c.1758T>G (RAF1)	ENSP00000509968.1:p.Ala586=
ENST00000685697.1:n.2493T>G (RAF1)
ENST00000685738.1:c.*722T>G (RAF1)	ENSP00000510156.1:n.*722T>G
ENST00000686409.1:n.5167T>G (RAF1)
ENST00000686455.1:n.4479T>G (RAF1)
ENST00000686762.1:c.*317T>G (RAF1)	ENSP00000509767.1:n.*317T>G
ENST00000687257.1:n.4212T>G (RAF1)
ENST00000687326.1:c.*3050T>G (RAF1)	ENSP00000509665.1:n.*3050T>G
ENST00000687505.1:n.1876T>G (RAF1)
ENST00000687923.1:c.1647T>G (RAF1)	ENSP00000510255.1:p.Ala549=
ENST00000688269.1:n.2354T>G (RAF1)
ENST00000688444.1:n.3875T>G (RAF1)
ENST00000688543.1:c.1659T>G (RAF1)	ENSP00000509612.1:p.Ala553=
ENST00000688625.1:c.*3127T>G (RAF1)	ENSP00000509522.1:n.*3127T>G
ENST00000688803.1:n.3186T>G (RAF1)
ENST00000688914.1:n.1171T>G (RAF1)
ENST00000689097.1:c.*1435T>G (RAF1)	ENSP00000509756.1:n.*1435T>G
ENST00000689389.1:c.1581T>G (RAF1)	ENSP00000510213.1:p.Ala527=
ENST00000689418.1:c.*3653T>G (RAF1)	ENSP00000509467.1:n.*3653T>G
ENST00000689540.1:n.4126T>G (RAF1)
ENST00000689876.1:c.*307T>G (RAF1)	ENSP00000508535.1:n.*307T>G
ENST00000689914.1:c.*692T>G (RAF1)	ENSP00000509847.1:n.*692T>G
ENST00000690397.1:c.1647T>G (RAF1)	ENSP00000508730.1:p.Ala549=
ENST00000690460.1:c.1746T>G (RAF1)	ENSP00000509106.1:p.Ala582=
ENST00000690585.1:c.484T>G (RAF1)
ENST00000690625.1:n.2794T>G (RAF1)
ENST00000691396.1:c.*1630T>G (RAF1)	ENSP00000510712.1:n.*1630T>G
ENST00000691643.1:n.2811T>G (RAF1)
ENST00000691724.1:c.*715T>G (RAF1)	ENSP00000509255.1:n.*715T>G
ENST00000691779.1:c.*1336T>G (RAF1)	ENSP00000508592.1:n.*1336T>G
ENST00000691888.1:c.632T>G (RAF1)
ENST00000691899.1:c.1758T>G (RAF1)	ENSP00000508763.1:p.Ala586=
ENST00000692069.1:n.4682T>G (RAF1)
ENST00000692093.1:c.1659T>G (RAF1)	ENSP00000509669.1:p.Ala553=
ENST00000692311.1:n.2582T>G (RAF1)
ENST00000692558.1:n.4341T>G (RAF1)
ENST00000692773.1:c.*1495T>G (RAF1)	ENSP00000509055.1:n.*1495T>G
ENST00000692830.1:c.*1503T>G (RAF1)	ENSP00000509461.1:n.*1503T>G
ENST00000693312.1:c.1533T>G (RAF1)	ENSP00000508686.1:p.Ala511=
ENST00000693664.1:c.*209T>G (RAF1)	ENSP00000509614.1:n.*209T>G
ENST00000693705.1:c.*1137T>G (RAF1)	ENSP00000510697.1:n.*1137T>G
ENST00000251849.9:c.1758T>G (RAF1) MANE Select	ENSP00000251849.4:p.Ala586=
ENST00000442415.7:c.1818T>G (RAF1)	ENSP00000401888.2:p.Ala606=
ENST00000676541.1:c.*2639A>C (MKRN2)	ENSP00000503730.1:n.*2639A>C
ENST00000677142.1:c.*2639A>C (MKRN2)	ENSP00000504455.1:n.*2639A>C
ENST00000677816.1:c.*1194A>C (MKRN2)	ENSP00000502893.1:n.*1194A>C
ENST00000677941.1:n.2702A>C (MKRN2)
ENST00000251849.8:c.1758T>G (RAF1)	ENSP00000251849.4:p.Ala586=
ENST00000423275.5:c.*1435T>G (RAF1)	ENSP00000401088.1:n.*1435T>G
ENST00000432427.2:c.1395T>G (RAF1)	ENSP00000398591.2:p.Ala465=
ENST00000442415.6:c.1818T>G (RAF1)	ENSP00000401888.2:p.Ala606=
ENST00000471449.1:n.447T>G (RAF1)
NM_002880.3:c.1758T>G , LRG_413t1:c.1758T>G (RAF1)	NP_002871.1:p.Ala586=
XM_005265355.1:c.1758T>G (RAF1)	XP_005265412.1:p.Ala586=
XM_005265357.1:c.1659T>G (RAF1)	XP_005265414.1:p.Ala553=
XM_005265358.3:c.1515T>G (RAF1)	XP_005265415.1:p.Ala505=
XM_005265359.3:c.1416T>G (RAF1)	XP_005265416.1:p.Ala472=
XM_011533974.1:c.1758T>G (RAF1)	XP_011532276.1:p.Ala586=
XM_011533975.1:c.1515T>G (RAF1)	XP_011532277.1:p.Ala505=
NM_001354689.1:c.1818T>G (RAF1)	NP_001341618.1:p.Ala606=
NM_001354690.1:c.1758T>G (RAF1)	NP_001341619.1:p.Ala586=
NM_001354691.1:c.1515T>G (RAF1)	NP_001341620.1:p.Ala505=
NM_001354692.1:c.1515T>G (RAF1)	NP_001341621.1:p.Ala505=
NM_001354693.1:c.1659T>G (RAF1)	NP_001341622.1:p.Ala553=
NM_001354694.1:c.1575T>G (RAF1)	NP_001341623.1:p.Ala525=
NM_001354695.1:c.1416T>G (RAF1)	NP_001341624.1:p.Ala472=
NR_148940.1:n.2286T>G (RAF1)
NR_148941.1:n.2232T>G (RAF1)
NR_148942.1:n.2171T>G (RAF1)
XM_011533974.3:c.1758T>G (RAF1)	XP_011532276.1:p.Ala586=
XM_017006966.1:c.1659T>G (RAF1)	XP_016862455.1:p.Ala553=
NM_001354689.3:c.1818T>G (RAF1)	NP_001341618.1:p.Ala606=
NM_001354690.2:c.1758T>G (RAF1)	NP_001341619.1:p.Ala586=
NM_001354691.2:c.1515T>G (RAF1)	NP_001341620.1:p.Ala505=
NM_001354692.2:c.1515T>G (RAF1)	NP_001341621.1:p.Ala505=
NM_001354693.2:c.1659T>G (RAF1)	NP_001341622.1:p.Ala553=
NM_001354694.2:c.1575T>G (RAF1)	NP_001341623.1:p.Ala525=
NM_001354695.2:c.1416T>G (RAF1)	NP_001341624.1:p.Ala472=
NR_148940.2:n.2202T>G (RAF1)
NR_148941.2:n.2148T>G (RAF1)
NR_148942.2:n.2087T>G (RAF1)
NM_001354690.3:c.1758T>G (RAF1)	NP_001341619.1:p.Ala586=
NM_001354691.3:c.1515T>G (RAF1)	NP_001341620.1:p.Ala505=
NM_001354692.3:c.1515T>G (RAF1)	NP_001341621.1:p.Ala505=
NM_001354693.3:c.1659T>G (RAF1)	NP_001341622.1:p.Ala553=
NM_001354694.3:c.1575T>G (RAF1)	NP_001341623.1:p.Ala525=
NM_001354695.3:c.1416T>G (RAF1)	NP_001341624.1:p.Ala472=
NM_002880.4:c.1758T>G (RAF1) MANE Select	NP_002871.1:p.Ala586=
NR_148940.3:n.2202T>G (RAF1)
NR_148941.3:n.2148T>G (RAF1)
NR_148942.3:n.2087T>G (RAF1)