Canonical Allele Identifier: CA69601822

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs763229187
• gnomAD v2: 3-12625846-T-C
• gnomAD v3: 3-12584347-T-C
• gnomAD v4: 3-12584347-T-C
• MyVariant Identifiers: chr3:g.12625846T>C (hg19) ; chr3:g.12584347T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584347T>C , CM000665.2:g.12584347T>C	GRCh38
NC_000003.11:g.12625846T>C , CM000665.1:g.12625846T>C	GRCh37
NC_000003.10:g.12600846T>C	NCBI36
NG_007467.1:g.84833A>G , LRG_413:g.84833A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1779A>G (RAF1)	ENSP00000401088.1:n.*1779A>G
ENST00000432427.3:c.1431A>G (RAF1)
ENST00000460610.2:n.6426A>G (RAF1)
ENST00000471449.2:n.924A>G (RAF1)
ENST00000475353.2:n.4394A>G (RAF1)
ENST00000684903.1:c.*1791A>G (RAF1)	ENSP00000508612.1:n.*1791A>G
ENST00000685348.1:c.*1825A>G (RAF1)	ENSP00000510285.1:n.*1825A>G
ENST00000685437.1:c.*167A>G (RAF1)	ENSP00000508794.1:n.*167A>G
ENST00000685653.1:c.*167A>G (RAF1)	ENSP00000509968.1:n.*167A>G
ENST00000685697.1:n.2849A>G (RAF1)
ENST00000685738.1:c.*1078A>G (RAF1)	ENSP00000510156.1:n.*1078A>G
ENST00000686409.1:n.5523A>G (RAF1)
ENST00000686455.1:n.4835A>G (RAF1)
ENST00000686762.1:c.*673A>G (RAF1)	ENSP00000509767.1:n.*673A>G
ENST00000687257.1:n.4568A>G (RAF1)
ENST00000687326.1:c.*3406A>G (RAF1)	ENSP00000509665.1:n.*3406A>G
ENST00000687505.1:n.2232A>G (RAF1)
ENST00000687923.1:c.*167A>G (RAF1)	ENSP00000510255.1:n.*167A>G
ENST00000688269.1:n.2710A>G (RAF1)
ENST00000688444.1:n.4231A>G (RAF1)
ENST00000688543.1:c.*167A>G (RAF1)	ENSP00000509612.1:n.*167A>G
ENST00000688625.1:c.*3483A>G (RAF1)	ENSP00000509522.1:n.*3483A>G
ENST00000688803.1:n.3542A>G (RAF1)
ENST00000689097.1:c.*1791A>G (RAF1)	ENSP00000509756.1:n.*1791A>G
ENST00000689389.1:c.*167A>G (RAF1)	ENSP00000510213.1:n.*167A>G
ENST00000689418.1:c.*4009A>G (RAF1)	ENSP00000509467.1:n.*4009A>G
ENST00000689540.1:n.4482A>G (RAF1)
ENST00000689876.1:c.*663A>G (RAF1)	ENSP00000508535.1:n.*663A>G
ENST00000689914.1:c.*1048A>G (RAF1)	ENSP00000509847.1:n.*1048A>G
ENST00000690397.1:c.*167A>G (RAF1)	ENSP00000508730.1:n.*167A>G
ENST00000690460.1:c.*167A>G (RAF1)	ENSP00000509106.1:n.*167A>G
ENST00000690585.1:c.840A>G (RAF1)
ENST00000690625.1:n.3150A>G (RAF1)
ENST00000691396.1:c.*1986A>G (RAF1)	ENSP00000510712.1:n.*1986A>G
ENST00000691643.1:n.3167A>G (RAF1)
ENST00000691724.1:c.*1071A>G (RAF1)	ENSP00000509255.1:n.*1071A>G
ENST00000691779.1:c.*1692A>G (RAF1)	ENSP00000508592.1:n.*1692A>G
ENST00000691888.1:c.988A>G (RAF1)
ENST00000691899.1:c.*167A>G (RAF1)	ENSP00000508763.1:n.*167A>G
ENST00000692069.1:n.5038A>G (RAF1)
ENST00000692093.1:c.*167A>G (RAF1)	ENSP00000509669.1:n.*167A>G
ENST00000692311.1:n.2938A>G (RAF1)
ENST00000692558.1:n.4697A>G (RAF1)
ENST00000692773.1:c.*1851A>G (RAF1)	ENSP00000509055.1:n.*1851A>G
ENST00000692830.1:c.*1859A>G (RAF1)	ENSP00000509461.1:n.*1859A>G
ENST00000693312.1:c.*167A>G (RAF1)	ENSP00000508686.1:n.*167A>G
ENST00000693664.1:c.*565A>G (RAF1)	ENSP00000509614.1:n.*565A>G
ENST00000693705.1:c.*1493A>G (RAF1)	ENSP00000510697.1:n.*1493A>G
ENST00000251849.9:c.*167A>G (RAF1) MANE Select	ENSP00000251849.4:n.*167A>G
ENST00000442415.7:c.*167A>G (RAF1)	ENSP00000401888.2:n.*167A>G
ENST00000676541.1:c.*2094T>C (MKRN2)	ENSP00000503730.1:n.*2094T>C
ENST00000677142.1:c.*2094T>C (MKRN2)	ENSP00000504455.1:n.*2094T>C
ENST00000677816.1:c.*649T>C (MKRN2)	ENSP00000502893.1:n.*649T>C
ENST00000677941.1:n.2157T>C (MKRN2)
ENST00000251849.8:c.*167A>G (RAF1)	ENSP00000251849.4:n.*167A>G
ENST00000423275.5:c.*1791A>G (RAF1)	ENSP00000401088.1:n.*1791A>G
ENST00000432427.2:c.1751A>G (RAF1)	ENSP00000398591.2:n.1751A>G
ENST00000442415.6:c.*167A>G (RAF1)	ENSP00000401888.2:n.*167A>G
ENST00000471449.1:n.803A>G (RAF1)
NM_002880.3:c.*167A>G , LRG_413t1:c.*167A>G (RAF1)	NP_002871.1:n.*167A>G
XM_005265355.1:c.*167A>G (RAF1)	XP_005265412.1:n.*167A>G
XM_005265357.1:c.*167A>G (RAF1)	XP_005265414.1:n.*167A>G
XM_005265358.3:c.*167A>G (RAF1)	XP_005265415.1:n.*167A>G
XM_005265359.3:c.*167A>G (RAF1)	XP_005265416.1:n.*167A>G
XM_011533974.1:c.*167A>G (RAF1)	XP_011532276.1:n.*167A>G
XM_011533975.1:c.*167A>G (RAF1)	XP_011532277.1:n.*167A>G
NM_001354689.1:c.*167A>G (RAF1)	NP_001341618.1:n.*167A>G
NM_001354690.1:c.*167A>G (RAF1)	NP_001341619.1:n.*167A>G
NM_001354691.1:c.*167A>G (RAF1)	NP_001341620.1:n.*167A>G
NM_001354692.1:c.*167A>G (RAF1)	NP_001341621.1:n.*167A>G
NM_001354693.1:c.*167A>G (RAF1)	NP_001341622.1:n.*167A>G
NM_001354694.1:c.*167A>G (RAF1)	NP_001341623.1:n.*167A>G
NM_001354695.1:c.*167A>G (RAF1)	NP_001341624.1:n.*167A>G
NR_148940.1:n.2642A>G (RAF1)
NR_148941.1:n.2588A>G (RAF1)
NR_148942.1:n.2527A>G (RAF1)
XM_011533974.3:c.*167A>G (RAF1)	XP_011532276.1:n.*167A>G
XM_017006966.1:c.*167A>G (RAF1)	XP_016862455.1:n.*167A>G
NM_001354689.3:c.*167A>G (RAF1)	NP_001341618.1:n.*167A>G
NM_001354690.2:c.*167A>G (RAF1)	NP_001341619.1:n.*167A>G
NM_001354691.2:c.*167A>G (RAF1)	NP_001341620.1:n.*167A>G
NM_001354692.2:c.*167A>G (RAF1)	NP_001341621.1:n.*167A>G
NM_001354693.2:c.*167A>G (RAF1)	NP_001341622.1:n.*167A>G
NM_001354694.2:c.*167A>G (RAF1)	NP_001341623.1:n.*167A>G
NM_001354695.2:c.*167A>G (RAF1)	NP_001341624.1:n.*167A>G
NR_148940.2:n.2558A>G (RAF1)
NR_148941.2:n.2504A>G (RAF1)
NR_148942.2:n.2443A>G (RAF1)
NM_001354690.3:c.*167A>G (RAF1)	NP_001341619.1:n.*167A>G
NM_001354691.3:c.*167A>G (RAF1)	NP_001341620.1:n.*167A>G
NM_001354692.3:c.*167A>G (RAF1)	NP_001341621.1:n.*167A>G
NM_001354693.3:c.*167A>G (RAF1)	NP_001341622.1:n.*167A>G
NM_001354694.3:c.*167A>G (RAF1)	NP_001341623.1:n.*167A>G
NM_001354695.3:c.*167A>G (RAF1)	NP_001341624.1:n.*167A>G
NM_002880.4:c.*167A>G (RAF1) MANE Select	NP_002871.1:n.*167A>G
NR_148940.3:n.2558A>G (RAF1)
NR_148941.3:n.2504A>G (RAF1)
NR_148942.3:n.2443A>G (RAF1)