Canonical Allele Identifier: CA351496805

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626427A>C (hg19) ; chr3:g.12584928A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584928A>C , CM000665.2:g.12584928A>C	GRCh38
NC_000003.11:g.12626427A>C , CM000665.1:g.12626427A>C	GRCh37
NC_000003.10:g.12601427A>C	NCBI36
NG_007467.1:g.84252T>G , LRG_413:g.84252T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1387T>G (RAF1)	ENSP00000401088.1:n.*1387T>G
ENST00000432427.3:c.1039T>G (RAF1)
ENST00000460610.2:n.6034T>G (RAF1)
ENST00000471449.2:n.532T>G (RAF1)
ENST00000475353.2:n.4002T>G (RAF1)
ENST00000684903.1:c.*1399T>G (RAF1)	ENSP00000508612.1:n.*1399T>G
ENST00000685348.1:c.*1433T>G (RAF1)	ENSP00000510285.1:n.*1433T>G
ENST00000685437.1:c.1623T>G (RAF1)	ENSP00000508794.1:p.Tyr541Ter
ENST00000685653.1:c.1722T>G (RAF1)	ENSP00000509968.1:p.Tyr574Ter
ENST00000685697.1:n.2457T>G (RAF1)
ENST00000685738.1:c.*686T>G (RAF1)	ENSP00000510156.1:n.*686T>G
ENST00000686409.1:n.5131T>G (RAF1)
ENST00000686455.1:n.4443T>G (RAF1)
ENST00000686762.1:c.*281T>G (RAF1)	ENSP00000509767.1:n.*281T>G
ENST00000687257.1:n.4176T>G (RAF1)
ENST00000687326.1:c.*3014T>G (RAF1)	ENSP00000509665.1:n.*3014T>G
ENST00000687505.1:n.1840T>G (RAF1)
ENST00000687923.1:c.1611T>G (RAF1)	ENSP00000510255.1:p.Tyr537Ter
ENST00000688269.1:n.2318T>G (RAF1)
ENST00000688444.1:n.3839T>G (RAF1)
ENST00000688543.1:c.1623T>G (RAF1)	ENSP00000509612.1:p.Tyr541Ter
ENST00000688625.1:c.*3091T>G (RAF1)	ENSP00000509522.1:n.*3091T>G
ENST00000688803.1:n.3150T>G (RAF1)
ENST00000688914.1:n.1135T>G (RAF1)
ENST00000689097.1:c.*1399T>G (RAF1)	ENSP00000509756.1:n.*1399T>G
ENST00000689389.1:c.1545T>G (RAF1)	ENSP00000510213.1:p.Tyr515Ter
ENST00000689418.1:c.*3617T>G (RAF1)	ENSP00000509467.1:n.*3617T>G
ENST00000689540.1:n.4090T>G (RAF1)
ENST00000689876.1:c.*271T>G (RAF1)	ENSP00000508535.1:n.*271T>G
ENST00000689914.1:c.*656T>G (RAF1)	ENSP00000509847.1:n.*656T>G
ENST00000690397.1:c.1611T>G (RAF1)	ENSP00000508730.1:p.Tyr537Ter
ENST00000690460.1:c.1710T>G (RAF1)	ENSP00000509106.1:p.Tyr570Ter
ENST00000690585.1:c.448T>G (RAF1)
ENST00000690625.1:n.2758T>G (RAF1)
ENST00000691396.1:c.*1594T>G (RAF1)	ENSP00000510712.1:n.*1594T>G
ENST00000691643.1:n.2775T>G (RAF1)
ENST00000691724.1:c.*679T>G (RAF1)	ENSP00000509255.1:n.*679T>G
ENST00000691779.1:c.*1300T>G (RAF1)	ENSP00000508592.1:n.*1300T>G
ENST00000691888.1:c.596T>G (RAF1)
ENST00000691899.1:c.1722T>G (RAF1)	ENSP00000508763.1:p.Tyr574Ter
ENST00000692069.1:n.4646T>G (RAF1)
ENST00000692093.1:c.1623T>G (RAF1)	ENSP00000509669.1:p.Tyr541Ter
ENST00000692311.1:n.2546T>G (RAF1)
ENST00000692558.1:n.4305T>G (RAF1)
ENST00000692773.1:c.*1459T>G (RAF1)	ENSP00000509055.1:n.*1459T>G
ENST00000692830.1:c.*1467T>G (RAF1)	ENSP00000509461.1:n.*1467T>G
ENST00000693312.1:c.1497T>G (RAF1)	ENSP00000508686.1:p.Tyr499Ter
ENST00000693664.1:c.*173T>G (RAF1)	ENSP00000509614.1:n.*173T>G
ENST00000693705.1:c.*1101T>G (RAF1)	ENSP00000510697.1:n.*1101T>G
ENST00000251849.9:c.1722T>G (RAF1) MANE Select	ENSP00000251849.4:p.Tyr574Ter
ENST00000442415.7:c.1782T>G (RAF1)	ENSP00000401888.2:p.Tyr594Ter
ENST00000676541.1:c.*2675A>C (MKRN2)	ENSP00000503730.1:n.*2675A>C
ENST00000677142.1:c.*2675A>C (MKRN2)	ENSP00000504455.1:n.*2675A>C
ENST00000677816.1:c.*1230A>C (MKRN2)	ENSP00000502893.1:n.*1230A>C
ENST00000677941.1:n.2738A>C (MKRN2)
ENST00000251849.8:c.1722T>G (RAF1)	ENSP00000251849.4:p.Tyr574Ter
ENST00000423275.5:c.*1399T>G (RAF1)	ENSP00000401088.1:n.*1399T>G
ENST00000432427.2:c.1359T>G (RAF1)	ENSP00000398591.2:p.Tyr453Ter
ENST00000442415.6:c.1782T>G (RAF1)	ENSP00000401888.2:p.Tyr594Ter
ENST00000471449.1:n.411T>G (RAF1)
NM_002880.3:c.1722T>G , LRG_413t1:c.1722T>G (RAF1)	NP_002871.1:p.Tyr574Ter
XM_005265355.1:c.1722T>G (RAF1)	XP_005265412.1:p.Tyr574Ter
XM_005265357.1:c.1623T>G (RAF1)	XP_005265414.1:p.Tyr541Ter
XM_005265358.3:c.1479T>G (RAF1)	XP_005265415.1:p.Tyr493Ter
XM_005265359.3:c.1380T>G (RAF1)	XP_005265416.1:p.Tyr460Ter
XM_011533974.1:c.1722T>G (RAF1)	XP_011532276.1:p.Tyr574Ter
XM_011533975.1:c.1479T>G (RAF1)	XP_011532277.1:p.Tyr493Ter
NM_001354689.1:c.1782T>G (RAF1)	NP_001341618.1:p.Tyr594Ter
NM_001354690.1:c.1722T>G (RAF1)	NP_001341619.1:p.Tyr574Ter
NM_001354691.1:c.1479T>G (RAF1)	NP_001341620.1:p.Tyr493Ter
NM_001354692.1:c.1479T>G (RAF1)	NP_001341621.1:p.Tyr493Ter
NM_001354693.1:c.1623T>G (RAF1)	NP_001341622.1:p.Tyr541Ter
NM_001354694.1:c.1539T>G (RAF1)	NP_001341623.1:p.Tyr513Ter
NM_001354695.1:c.1380T>G (RAF1)	NP_001341624.1:p.Tyr460Ter
NR_148940.1:n.2250T>G (RAF1)
NR_148941.1:n.2196T>G (RAF1)
NR_148942.1:n.2135T>G (RAF1)
XM_011533974.3:c.1722T>G (RAF1)	XP_011532276.1:p.Tyr574Ter
XM_017006966.1:c.1623T>G (RAF1)	XP_016862455.1:p.Tyr541Ter
NM_001354689.3:c.1782T>G (RAF1)	NP_001341618.1:p.Tyr594Ter
NM_001354690.2:c.1722T>G (RAF1)	NP_001341619.1:p.Tyr574Ter
NM_001354691.2:c.1479T>G (RAF1)	NP_001341620.1:p.Tyr493Ter
NM_001354692.2:c.1479T>G (RAF1)	NP_001341621.1:p.Tyr493Ter
NM_001354693.2:c.1623T>G (RAF1)	NP_001341622.1:p.Tyr541Ter
NM_001354694.2:c.1539T>G (RAF1)	NP_001341623.1:p.Tyr513Ter
NM_001354695.2:c.1380T>G (RAF1)	NP_001341624.1:p.Tyr460Ter
NR_148940.2:n.2166T>G (RAF1)
NR_148941.2:n.2112T>G (RAF1)
NR_148942.2:n.2051T>G (RAF1)
NM_001354690.3:c.1722T>G (RAF1)	NP_001341619.1:p.Tyr574Ter
NM_001354691.3:c.1479T>G (RAF1)	NP_001341620.1:p.Tyr493Ter
NM_001354692.3:c.1479T>G (RAF1)	NP_001341621.1:p.Tyr493Ter
NM_001354693.3:c.1623T>G (RAF1)	NP_001341622.1:p.Tyr541Ter
NM_001354694.3:c.1539T>G (RAF1)	NP_001341623.1:p.Tyr513Ter
NM_001354695.3:c.1380T>G (RAF1)	NP_001341624.1:p.Tyr460Ter
NM_002880.4:c.1722T>G (RAF1) MANE Select	NP_002871.1:p.Tyr574Ter
NR_148940.3:n.2166T>G (RAF1)
NR_148941.3:n.2112T>G (RAF1)
NR_148942.3:n.2051T>G (RAF1)