Canonical Allele Identifier: CA351497038

Gene: RAF1 MKRN2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1344T>C (RAF1)	ENSP00000401088.1:n.*1344T>C
ENST00000432427.3:c.996T>C (RAF1)
ENST00000460610.2:n.5991T>C (RAF1)
ENST00000471449.2:n.489T>C (RAF1)
ENST00000475353.2:n.3959T>C (RAF1)
ENST00000684903.1:c.*1356T>C (RAF1)	ENSP00000508612.1:n.*1356T>C
ENST00000685348.1:c.*1390T>C (RAF1)	ENSP00000510285.1:n.*1390T>C
ENST00000685437.1:c.1580T>C (RAF1)	ENSP00000508794.1:p.Met527Thr
ENST00000685653.1:c.1679T>C (RAF1)	ENSP00000509968.1:p.Met560Thr
ENST00000685697.1:n.2414T>C (RAF1)
ENST00000685738.1:c.*643T>C (RAF1)	ENSP00000510156.1:n.*643T>C
ENST00000686409.1:n.5088T>C (RAF1)
ENST00000686455.1:n.4400T>C (RAF1)
ENST00000686762.1:c.*238T>C (RAF1)	ENSP00000509767.1:n.*238T>C
ENST00000687257.1:n.4133T>C (RAF1)
ENST00000687326.1:c.*2971T>C (RAF1)	ENSP00000509665.1:n.*2971T>C
ENST00000687505.1:n.1797T>C (RAF1)
ENST00000687923.1:c.1568T>C (RAF1)	ENSP00000510255.1:p.Met523Thr
ENST00000688269.1:n.2275T>C (RAF1)
ENST00000688444.1:n.3796T>C (RAF1)
ENST00000688543.1:c.1580T>C (RAF1)	ENSP00000509612.1:p.Met527Thr
ENST00000688625.1:c.*3048T>C (RAF1)	ENSP00000509522.1:n.*3048T>C
ENST00000688803.1:n.3107T>C (RAF1)
ENST00000688914.1:n.1092T>C (RAF1)
ENST00000689097.1:c.*1356T>C (RAF1)	ENSP00000509756.1:n.*1356T>C
ENST00000689389.1:c.1502T>C (RAF1)	ENSP00000510213.1:p.Met501Thr
ENST00000689418.1:c.*3574T>C (RAF1)	ENSP00000509467.1:n.*3574T>C
ENST00000689540.1:n.4047T>C (RAF1)
ENST00000689876.1:c.*228T>C (RAF1)	ENSP00000508535.1:n.*228T>C
ENST00000689914.1:c.*613T>C (RAF1)	ENSP00000509847.1:n.*613T>C
ENST00000690397.1:c.1568T>C (RAF1)	ENSP00000508730.1:p.Met523Thr
ENST00000690460.1:c.1667T>C (RAF1)	ENSP00000509106.1:p.Met556Thr
ENST00000690585.1:c.405T>C (RAF1)
ENST00000690625.1:n.2715T>C (RAF1)
ENST00000691396.1:c.*1551T>C (RAF1)	ENSP00000510712.1:n.*1551T>C
ENST00000691643.1:n.2732T>C (RAF1)
ENST00000691724.1:c.*636T>C (RAF1)	ENSP00000509255.1:n.*636T>C
ENST00000691779.1:c.*1257T>C (RAF1)	ENSP00000508592.1:n.*1257T>C
ENST00000691888.1:c.553T>C (RAF1)
ENST00000691899.1:c.1679T>C (RAF1)	ENSP00000508763.1:p.Met560Thr
ENST00000692069.1:n.4603T>C (RAF1)
ENST00000692093.1:c.1580T>C (RAF1)	ENSP00000509669.1:p.Met527Thr
ENST00000692311.1:n.2503T>C (RAF1)
ENST00000692558.1:n.4262T>C (RAF1)
ENST00000692773.1:c.*1416T>C (RAF1)	ENSP00000509055.1:n.*1416T>C
ENST00000692830.1:c.*1424T>C (RAF1)	ENSP00000509461.1:n.*1424T>C
ENST00000693312.1:c.1454T>C (RAF1)	ENSP00000508686.1:p.Met485Thr
ENST00000693664.1:c.*130T>C (RAF1)	ENSP00000509614.1:n.*130T>C
ENST00000693705.1:c.*1058T>C (RAF1)	ENSP00000510697.1:n.*1058T>C
ENST00000251849.9:c.1679T>C (RAF1) MANE Select	ENSP00000251849.4:p.Met560Thr
ENST00000442415.7:c.1739T>C (RAF1)	ENSP00000401888.2:p.Met580Thr
ENST00000676541.1:c.*2718A>G (MKRN2)	ENSP00000503730.1:n.*2718A>G
ENST00000677142.1:c.*2718A>G (MKRN2)	ENSP00000504455.1:n.*2718A>G
ENST00000677816.1:c.*1273A>G (MKRN2)	ENSP00000502893.1:n.*1273A>G
ENST00000677941.1:n.2781A>G (MKRN2)
ENST00000251849.8:c.1679T>C (RAF1)	ENSP00000251849.4:p.Met560Thr
ENST00000423275.5:c.*1356T>C (RAF1)	ENSP00000401088.1:n.*1356T>C
ENST00000432427.2:c.1316T>C (RAF1)	ENSP00000398591.2:p.Met439Thr
ENST00000442415.6:c.1739T>C (RAF1)	ENSP00000401888.2:p.Met580Thr
ENST00000471449.1:n.368T>C (RAF1)
NM_002880.3:c.1679T>C , LRG_413t1:c.1679T>C (RAF1)	NP_002871.1:p.Met560Thr
XM_005265355.1:c.1679T>C (RAF1)	XP_005265412.1:p.Met560Thr
XM_005265357.1:c.1580T>C (RAF1)	XP_005265414.1:p.Met527Thr
XM_005265358.3:c.1436T>C (RAF1)	XP_005265415.1:p.Met479Thr
XM_005265359.3:c.1337T>C (RAF1)	XP_005265416.1:p.Met446Thr
XM_011533974.1:c.1679T>C (RAF1)	XP_011532276.1:p.Met560Thr
XM_011533975.1:c.1436T>C (RAF1)	XP_011532277.1:p.Met479Thr
NM_001354689.1:c.1739T>C (RAF1)	NP_001341618.1:p.Met580Thr
NM_001354690.1:c.1679T>C (RAF1)	NP_001341619.1:p.Met560Thr
NM_001354691.1:c.1436T>C (RAF1)	NP_001341620.1:p.Met479Thr
NM_001354692.1:c.1436T>C (RAF1)	NP_001341621.1:p.Met479Thr
NM_001354693.1:c.1580T>C (RAF1)	NP_001341622.1:p.Met527Thr
NM_001354694.1:c.1496T>C (RAF1)	NP_001341623.1:p.Met499Thr
NM_001354695.1:c.1337T>C (RAF1)	NP_001341624.1:p.Met446Thr
NR_148940.1:n.2207T>C (RAF1)
NR_148941.1:n.2153T>C (RAF1)
NR_148942.1:n.2092T>C (RAF1)
XM_011533974.3:c.1679T>C (RAF1)	XP_011532276.1:p.Met560Thr
XM_017006966.1:c.1580T>C (RAF1)	XP_016862455.1:p.Met527Thr
NM_001354689.3:c.1739T>C (RAF1)	NP_001341618.1:p.Met580Thr
NM_001354690.2:c.1679T>C (RAF1)	NP_001341619.1:p.Met560Thr
NM_001354691.2:c.1436T>C (RAF1)	NP_001341620.1:p.Met479Thr
NM_001354692.2:c.1436T>C (RAF1)	NP_001341621.1:p.Met479Thr
NM_001354693.2:c.1580T>C (RAF1)	NP_001341622.1:p.Met527Thr
NM_001354694.2:c.1496T>C (RAF1)	NP_001341623.1:p.Met499Thr
NM_001354695.2:c.1337T>C (RAF1)	NP_001341624.1:p.Met446Thr
NR_148940.2:n.2123T>C (RAF1)
NR_148941.2:n.2069T>C (RAF1)
NR_148942.2:n.2008T>C (RAF1)
NM_001354690.3:c.1679T>C (RAF1)	NP_001341619.1:p.Met560Thr
NM_001354691.3:c.1436T>C (RAF1)	NP_001341620.1:p.Met479Thr
NM_001354692.3:c.1436T>C (RAF1)	NP_001341621.1:p.Met479Thr
NM_001354693.3:c.1580T>C (RAF1)	NP_001341622.1:p.Met527Thr
NM_001354694.3:c.1496T>C (RAF1)	NP_001341623.1:p.Met499Thr
NM_001354695.3:c.1337T>C (RAF1)	NP_001341624.1:p.Met446Thr
NM_002880.4:c.1679T>C (RAF1) MANE Select	NP_002871.1:p.Met560Thr
NR_148940.3:n.2123T>C (RAF1)
NR_148941.3:n.2069T>C (RAF1)
NR_148942.3:n.2008T>C (RAF1)