Canonical Allele Identifier: CA351497034

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626470A>T (hg19) ; chr3:g.12584971A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584971A>T , CM000665.2:g.12584971A>T	GRCh38
NC_000003.11:g.12626470A>T , CM000665.1:g.12626470A>T	GRCh37
NC_000003.10:g.12601470A>T	NCBI36
NG_007467.1:g.84209T>A , LRG_413:g.84209T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1344T>A (RAF1)	ENSP00000401088.1:n.*1344T>A
ENST00000432427.3:c.996T>A (RAF1)
ENST00000460610.2:n.5991T>A (RAF1)
ENST00000471449.2:n.489T>A (RAF1)
ENST00000475353.2:n.3959T>A (RAF1)
ENST00000684903.1:c.*1356T>A (RAF1)	ENSP00000508612.1:n.*1356T>A
ENST00000685348.1:c.*1390T>A (RAF1)	ENSP00000510285.1:n.*1390T>A
ENST00000685437.1:c.1580T>A (RAF1)	ENSP00000508794.1:p.Met527Lys
ENST00000685653.1:c.1679T>A (RAF1)	ENSP00000509968.1:p.Met560Lys
ENST00000685697.1:n.2414T>A (RAF1)
ENST00000685738.1:c.*643T>A (RAF1)	ENSP00000510156.1:n.*643T>A
ENST00000686409.1:n.5088T>A (RAF1)
ENST00000686455.1:n.4400T>A (RAF1)
ENST00000686762.1:c.*238T>A (RAF1)	ENSP00000509767.1:n.*238T>A
ENST00000687257.1:n.4133T>A (RAF1)
ENST00000687326.1:c.*2971T>A (RAF1)	ENSP00000509665.1:n.*2971T>A
ENST00000687505.1:n.1797T>A (RAF1)
ENST00000687923.1:c.1568T>A (RAF1)	ENSP00000510255.1:p.Met523Lys
ENST00000688269.1:n.2275T>A (RAF1)
ENST00000688444.1:n.3796T>A (RAF1)
ENST00000688543.1:c.1580T>A (RAF1)	ENSP00000509612.1:p.Met527Lys
ENST00000688625.1:c.*3048T>A (RAF1)	ENSP00000509522.1:n.*3048T>A
ENST00000688803.1:n.3107T>A (RAF1)
ENST00000688914.1:n.1092T>A (RAF1)
ENST00000689097.1:c.*1356T>A (RAF1)	ENSP00000509756.1:n.*1356T>A
ENST00000689389.1:c.1502T>A (RAF1)	ENSP00000510213.1:p.Met501Lys
ENST00000689418.1:c.*3574T>A (RAF1)	ENSP00000509467.1:n.*3574T>A
ENST00000689540.1:n.4047T>A (RAF1)
ENST00000689876.1:c.*228T>A (RAF1)	ENSP00000508535.1:n.*228T>A
ENST00000689914.1:c.*613T>A (RAF1)	ENSP00000509847.1:n.*613T>A
ENST00000690397.1:c.1568T>A (RAF1)	ENSP00000508730.1:p.Met523Lys
ENST00000690460.1:c.1667T>A (RAF1)	ENSP00000509106.1:p.Met556Lys
ENST00000690585.1:c.405T>A (RAF1)
ENST00000690625.1:n.2715T>A (RAF1)
ENST00000691396.1:c.*1551T>A (RAF1)	ENSP00000510712.1:n.*1551T>A
ENST00000691643.1:n.2732T>A (RAF1)
ENST00000691724.1:c.*636T>A (RAF1)	ENSP00000509255.1:n.*636T>A
ENST00000691779.1:c.*1257T>A (RAF1)	ENSP00000508592.1:n.*1257T>A
ENST00000691888.1:c.553T>A (RAF1)
ENST00000691899.1:c.1679T>A (RAF1)	ENSP00000508763.1:p.Met560Lys
ENST00000692069.1:n.4603T>A (RAF1)
ENST00000692093.1:c.1580T>A (RAF1)	ENSP00000509669.1:p.Met527Lys
ENST00000692311.1:n.2503T>A (RAF1)
ENST00000692558.1:n.4262T>A (RAF1)
ENST00000692773.1:c.*1416T>A (RAF1)	ENSP00000509055.1:n.*1416T>A
ENST00000692830.1:c.*1424T>A (RAF1)	ENSP00000509461.1:n.*1424T>A
ENST00000693312.1:c.1454T>A (RAF1)	ENSP00000508686.1:p.Met485Lys
ENST00000693664.1:c.*130T>A (RAF1)	ENSP00000509614.1:n.*130T>A
ENST00000693705.1:c.*1058T>A (RAF1)	ENSP00000510697.1:n.*1058T>A
ENST00000251849.9:c.1679T>A (RAF1) MANE Select	ENSP00000251849.4:p.Met560Lys
ENST00000442415.7:c.1739T>A (RAF1)	ENSP00000401888.2:p.Met580Lys
ENST00000676541.1:c.*2718A>T (MKRN2)	ENSP00000503730.1:n.*2718A>T
ENST00000677142.1:c.*2718A>T (MKRN2)	ENSP00000504455.1:n.*2718A>T
ENST00000677816.1:c.*1273A>T (MKRN2)	ENSP00000502893.1:n.*1273A>T
ENST00000677941.1:n.2781A>T (MKRN2)
ENST00000251849.8:c.1679T>A (RAF1)	ENSP00000251849.4:p.Met560Lys
ENST00000423275.5:c.*1356T>A (RAF1)	ENSP00000401088.1:n.*1356T>A
ENST00000432427.2:c.1316T>A (RAF1)	ENSP00000398591.2:p.Met439Lys
ENST00000442415.6:c.1739T>A (RAF1)	ENSP00000401888.2:p.Met580Lys
ENST00000471449.1:n.368T>A (RAF1)
NM_002880.3:c.1679T>A , LRG_413t1:c.1679T>A (RAF1)	NP_002871.1:p.Met560Lys
XM_005265355.1:c.1679T>A (RAF1)	XP_005265412.1:p.Met560Lys
XM_005265357.1:c.1580T>A (RAF1)	XP_005265414.1:p.Met527Lys
XM_005265358.3:c.1436T>A (RAF1)	XP_005265415.1:p.Met479Lys
XM_005265359.3:c.1337T>A (RAF1)	XP_005265416.1:p.Met446Lys
XM_011533974.1:c.1679T>A (RAF1)	XP_011532276.1:p.Met560Lys
XM_011533975.1:c.1436T>A (RAF1)	XP_011532277.1:p.Met479Lys
NM_001354689.1:c.1739T>A (RAF1)	NP_001341618.1:p.Met580Lys
NM_001354690.1:c.1679T>A (RAF1)	NP_001341619.1:p.Met560Lys
NM_001354691.1:c.1436T>A (RAF1)	NP_001341620.1:p.Met479Lys
NM_001354692.1:c.1436T>A (RAF1)	NP_001341621.1:p.Met479Lys
NM_001354693.1:c.1580T>A (RAF1)	NP_001341622.1:p.Met527Lys
NM_001354694.1:c.1496T>A (RAF1)	NP_001341623.1:p.Met499Lys
NM_001354695.1:c.1337T>A (RAF1)	NP_001341624.1:p.Met446Lys
NR_148940.1:n.2207T>A (RAF1)
NR_148941.1:n.2153T>A (RAF1)
NR_148942.1:n.2092T>A (RAF1)
XM_011533974.3:c.1679T>A (RAF1)	XP_011532276.1:p.Met560Lys
XM_017006966.1:c.1580T>A (RAF1)	XP_016862455.1:p.Met527Lys
NM_001354689.3:c.1739T>A (RAF1)	NP_001341618.1:p.Met580Lys
NM_001354690.2:c.1679T>A (RAF1)	NP_001341619.1:p.Met560Lys
NM_001354691.2:c.1436T>A (RAF1)	NP_001341620.1:p.Met479Lys
NM_001354692.2:c.1436T>A (RAF1)	NP_001341621.1:p.Met479Lys
NM_001354693.2:c.1580T>A (RAF1)	NP_001341622.1:p.Met527Lys
NM_001354694.2:c.1496T>A (RAF1)	NP_001341623.1:p.Met499Lys
NM_001354695.2:c.1337T>A (RAF1)	NP_001341624.1:p.Met446Lys
NR_148940.2:n.2123T>A (RAF1)
NR_148941.2:n.2069T>A (RAF1)
NR_148942.2:n.2008T>A (RAF1)
NM_001354690.3:c.1679T>A (RAF1)	NP_001341619.1:p.Met560Lys
NM_001354691.3:c.1436T>A (RAF1)	NP_001341620.1:p.Met479Lys
NM_001354692.3:c.1436T>A (RAF1)	NP_001341621.1:p.Met479Lys
NM_001354693.3:c.1580T>A (RAF1)	NP_001341622.1:p.Met527Lys
NM_001354694.3:c.1496T>A (RAF1)	NP_001341623.1:p.Met499Lys
NM_001354695.3:c.1337T>A (RAF1)	NP_001341624.1:p.Met446Lys
NM_002880.4:c.1679T>A (RAF1) MANE Select	NP_002871.1:p.Met560Lys
NR_148940.3:n.2123T>A (RAF1)
NR_148941.3:n.2069T>A (RAF1)
NR_148942.3:n.2008T>A (RAF1)