Canonical Allele Identifier: CA351502490

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632435T>G (hg19) ; chr3:g.12590936T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590936T>G , CM000665.2:g.12590936T>G	GRCh38
NC_000003.11:g.12632435T>G , CM000665.1:g.12632435T>G	GRCh37
NC_000003.10:g.12607435T>G	NCBI36
NG_007467.1:g.78244A>C , LRG_413:g.78244A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*897A>C	ENSP00000401088.1:n.*897A>C
ENST00000432427.3:c.549A>C
ENST00000460610.2:n.26A>C
ENST00000465826.6:n.823A>C
ENST00000475353.2:n.1154A>C
ENST00000494557.2:n.1043A>C
ENST00000684903.1:c.*909A>C	ENSP00000508612.1:n.*909A>C
ENST00000685348.1:c.*909A>C	ENSP00000510285.1:n.*909A>C
ENST00000685437.1:c.1133A>C	ENSP00000508794.1:p.Tyr378Ser
ENST00000685653.1:c.1232A>C	ENSP00000509968.1:p.Tyr411Ser
ENST00000685738.1:c.*196A>C	ENSP00000510156.1:n.*196A>C
ENST00000686409.1:n.2283A>C
ENST00000686455.1:n.1595A>C
ENST00000686762.1:c.1232A>C	ENSP00000509767.1:p.Tyr411Ser
ENST00000687257.1:n.1468A>C
ENST00000687326.1:c.*166A>C	ENSP00000509665.1:n.*166A>C
ENST00000687505.1:n.1350A>C
ENST00000687923.1:c.1121A>C	ENSP00000510255.1:p.Tyr374Ser
ENST00000687940.1:n.1609A>C
ENST00000688269.1:n.1828A>C
ENST00000688326.1:c.665A>C
ENST00000688444.1:n.1558A>C
ENST00000688543.1:c.1133A>C	ENSP00000509612.1:p.Tyr378Ser
ENST00000688625.1:c.*810A>C	ENSP00000509522.1:n.*810A>C
ENST00000688803.1:n.1463A>C
ENST00000688914.1:n.218A>C
ENST00000689097.1:c.*909A>C	ENSP00000509756.1:n.*909A>C
ENST00000689389.1:c.1193+772A>C	ENSP00000510213.1:n.1193+772A>C
ENST00000689418.1:c.*909A>C	ENSP00000509467.1:n.*909A>C
ENST00000689481.1:c.*909A>C	ENSP00000510248.1:n.*909A>C
ENST00000689540.1:n.1382A>C
ENST00000689876.1:c.1232A>C	ENSP00000508535.1:p.Tyr411Ser
ENST00000689914.1:c.*166A>C	ENSP00000509847.1:n.*166A>C
ENST00000690397.1:c.1121A>C	ENSP00000508730.1:p.Tyr374Ser
ENST00000690460.1:c.1220A>C	ENSP00000509106.1:p.Tyr407Ser
ENST00000690585.1:c.124A>C
ENST00000690625.1:n.2268A>C
ENST00000691396.1:c.*1084A>C	ENSP00000510712.1:n.*1084A>C
ENST00000691724.1:c.*189A>C	ENSP00000509255.1:n.*189A>C
ENST00000691779.1:c.*810A>C	ENSP00000508592.1:n.*810A>C
ENST00000691888.1:c.124A>C
ENST00000691899.1:c.1232A>C	ENSP00000508763.1:p.Tyr411Ser
ENST00000692069.1:n.1798A>C
ENST00000692093.1:c.1133A>C	ENSP00000509669.1:p.Tyr378Ser
ENST00000692311.1:n.2056A>C
ENST00000692558.1:n.1597A>C
ENST00000692773.1:c.*969A>C	ENSP00000509055.1:n.*969A>C
ENST00000692830.1:c.*977A>C	ENSP00000509461.1:n.*977A>C
ENST00000693069.1:c.*166A>C	ENSP00000510072.1:n.*166A>C
ENST00000693312.1:c.1007A>C	ENSP00000508686.1:p.Tyr336Ser
ENST00000693664.1:c.1232A>C	ENSP00000509614.1:p.Tyr411Ser
ENST00000693705.1:c.*909A>C	ENSP00000510697.1:n.*909A>C
ENST00000251849.9:c.1232A>C MANE Select	ENSP00000251849.4:p.Tyr411Ser
ENST00000442415.7:c.1292A>C	ENSP00000401888.2:p.Tyr431Ser
ENST00000251849.8:c.1232A>C	ENSP00000251849.4:p.Tyr411Ser
ENST00000423275.5:c.*909A>C	ENSP00000401088.1:n.*909A>C
ENST00000432427.2:c.869A>C	ENSP00000398591.2:p.Tyr290Ser
ENST00000442415.6:c.1292A>C	ENSP00000401888.2:p.Tyr431Ser
ENST00000460610.1:n.189A>C
ENST00000465826.5:n.589A>C
ENST00000475353.1:n.400A>C
ENST00000494557.1:n.248A>C
NM_002880.3:c.1232A>C , LRG_413t1:c.1232A>C	NP_002871.1:p.Tyr411Ser
XM_005265355.1:c.1232A>C	XP_005265412.1:p.Tyr411Ser
XM_005265357.1:c.1133A>C	XP_005265414.1:p.Tyr378Ser
XM_005265358.3:c.989A>C	XP_005265415.1:p.Tyr330Ser
XM_005265359.3:c.890A>C	XP_005265416.1:p.Tyr297Ser
XM_005265360.1:c.1232A>C	XP_005265417.1:p.Tyr411Ser
XM_011533974.1:c.1232A>C	XP_011532276.1:p.Tyr411Ser
XM_011533975.1:c.989A>C	XP_011532277.1:p.Tyr330Ser
NM_001354689.1:c.1292A>C	NP_001341618.1:p.Tyr431Ser
NM_001354690.1:c.1232A>C	NP_001341619.1:p.Tyr411Ser
NM_001354691.1:c.989A>C	NP_001341620.1:p.Tyr330Ser
NM_001354692.1:c.989A>C	NP_001341621.1:p.Tyr330Ser
NM_001354693.1:c.1133A>C	NP_001341622.1:p.Tyr378Ser
NM_001354694.1:c.1049A>C	NP_001341623.1:p.Tyr350Ser
NM_001354695.1:c.890A>C	NP_001341624.1:p.Tyr297Ser
NR_148940.1:n.1760A>C
NR_148941.1:n.1706A>C
NR_148942.1:n.1645A>C
XM_011533974.3:c.1232A>C	XP_011532276.1:p.Tyr411Ser
XM_017006966.1:c.1133A>C	XP_016862455.1:p.Tyr378Ser
NM_001354689.3:c.1292A>C	NP_001341618.1:p.Tyr431Ser
NM_001354690.2:c.1232A>C	NP_001341619.1:p.Tyr411Ser
NM_001354691.2:c.989A>C	NP_001341620.1:p.Tyr330Ser
NM_001354692.2:c.989A>C	NP_001341621.1:p.Tyr330Ser
NM_001354693.2:c.1133A>C	NP_001341622.1:p.Tyr378Ser
NM_001354694.2:c.1049A>C	NP_001341623.1:p.Tyr350Ser
NM_001354695.2:c.890A>C	NP_001341624.1:p.Tyr297Ser
NR_148940.2:n.1676A>C
NR_148941.2:n.1622A>C
NR_148942.2:n.1561A>C
NM_001354690.3:c.1232A>C	NP_001341619.1:p.Tyr411Ser
NM_001354691.3:c.989A>C	NP_001341620.1:p.Tyr330Ser
NM_001354692.3:c.989A>C	NP_001341621.1:p.Tyr330Ser
NM_001354693.3:c.1133A>C	NP_001341622.1:p.Tyr378Ser
NM_001354694.3:c.1049A>C	NP_001341623.1:p.Tyr350Ser
NM_001354695.3:c.890A>C	NP_001341624.1:p.Tyr297Ser
NM_002880.4:c.1232A>C MANE Select	NP_002871.1:p.Tyr411Ser
NR_148940.3:n.1676A>C
NR_148941.3:n.1622A>C
NR_148942.3:n.1561A>C