Canonical Allele Identifier: CA898402354

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs1385982925
• gnomAD v3: 3-12584426-G-T
• gnomAD v4: 3-12584426-G-T
• MyVariant Identifiers: chr3:g.12625925G>T (hg19) ; chr3:g.12584426G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584426G>T , CM000665.2:g.12584426G>T	GRCh38
NC_000003.11:g.12625925G>T , CM000665.1:g.12625925G>T	GRCh37
NC_000003.10:g.12600925G>T	NCBI36
NG_007467.1:g.84754C>A , LRG_413:g.84754C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1700C>A (RAF1)	ENSP00000401088.1:n.*1700C>A
ENST00000432427.3:c.1352C>A (RAF1)
ENST00000460610.2:n.6347C>A (RAF1)
ENST00000471449.2:n.845C>A (RAF1)
ENST00000475353.2:n.4315C>A (RAF1)
ENST00000684903.1:c.*1712C>A (RAF1)	ENSP00000508612.1:n.*1712C>A
ENST00000685348.1:c.*1746C>A (RAF1)	ENSP00000510285.1:n.*1746C>A
ENST00000685437.1:c.*88C>A (RAF1)	ENSP00000508794.1:n.*88C>A
ENST00000685653.1:c.*88C>A (RAF1)	ENSP00000509968.1:n.*88C>A
ENST00000685697.1:n.2770C>A (RAF1)
ENST00000685738.1:c.*999C>A (RAF1)	ENSP00000510156.1:n.*999C>A
ENST00000686409.1:n.5444C>A (RAF1)
ENST00000686455.1:n.4756C>A (RAF1)
ENST00000686762.1:c.*594C>A (RAF1)	ENSP00000509767.1:n.*594C>A
ENST00000687257.1:n.4489C>A (RAF1)
ENST00000687326.1:c.*3327C>A (RAF1)	ENSP00000509665.1:n.*3327C>A
ENST00000687505.1:n.2153C>A (RAF1)
ENST00000687923.1:c.*88C>A (RAF1)	ENSP00000510255.1:n.*88C>A
ENST00000688269.1:n.2631C>A (RAF1)
ENST00000688444.1:n.4152C>A (RAF1)
ENST00000688543.1:c.*88C>A (RAF1)	ENSP00000509612.1:n.*88C>A
ENST00000688625.1:c.*3404C>A (RAF1)	ENSP00000509522.1:n.*3404C>A
ENST00000688803.1:n.3463C>A (RAF1)
ENST00000689097.1:c.*1712C>A (RAF1)	ENSP00000509756.1:n.*1712C>A
ENST00000689389.1:c.*88C>A (RAF1)	ENSP00000510213.1:n.*88C>A
ENST00000689418.1:c.*3930C>A (RAF1)	ENSP00000509467.1:n.*3930C>A
ENST00000689540.1:n.4403C>A (RAF1)
ENST00000689876.1:c.*584C>A (RAF1)	ENSP00000508535.1:n.*584C>A
ENST00000689914.1:c.*969C>A (RAF1)	ENSP00000509847.1:n.*969C>A
ENST00000690397.1:c.*88C>A (RAF1)	ENSP00000508730.1:n.*88C>A
ENST00000690460.1:c.*88C>A (RAF1)	ENSP00000509106.1:n.*88C>A
ENST00000690585.1:c.761C>A (RAF1)
ENST00000690625.1:n.3071C>A (RAF1)
ENST00000691396.1:c.*1907C>A (RAF1)	ENSP00000510712.1:n.*1907C>A
ENST00000691643.1:n.3088C>A (RAF1)
ENST00000691724.1:c.*992C>A (RAF1)	ENSP00000509255.1:n.*992C>A
ENST00000691779.1:c.*1613C>A (RAF1)	ENSP00000508592.1:n.*1613C>A
ENST00000691888.1:c.909C>A (RAF1)
ENST00000691899.1:c.*88C>A (RAF1)	ENSP00000508763.1:n.*88C>A
ENST00000692069.1:n.4959C>A (RAF1)
ENST00000692093.1:c.*88C>A (RAF1)	ENSP00000509669.1:n.*88C>A
ENST00000692311.1:n.2859C>A (RAF1)
ENST00000692558.1:n.4618C>A (RAF1)
ENST00000692773.1:c.*1772C>A (RAF1)	ENSP00000509055.1:n.*1772C>A
ENST00000692830.1:c.*1780C>A (RAF1)	ENSP00000509461.1:n.*1780C>A
ENST00000693312.1:c.*88C>A (RAF1)	ENSP00000508686.1:n.*88C>A
ENST00000693664.1:c.*486C>A (RAF1)	ENSP00000509614.1:n.*486C>A
ENST00000693705.1:c.*1414C>A (RAF1)	ENSP00000510697.1:n.*1414C>A
ENST00000251849.9:c.*88C>A (RAF1) MANE Select	ENSP00000251849.4:n.*88C>A
ENST00000442415.7:c.*88C>A (RAF1)	ENSP00000401888.2:n.*88C>A
ENST00000676541.1:c.*2173G>T (MKRN2)	ENSP00000503730.1:n.*2173G>T
ENST00000677142.1:c.*2173G>T (MKRN2)	ENSP00000504455.1:n.*2173G>T
ENST00000677816.1:c.*728G>T (MKRN2)	ENSP00000502893.1:n.*728G>T
ENST00000677941.1:n.2236G>T (MKRN2)
ENST00000251849.8:c.*88C>A (RAF1)	ENSP00000251849.4:n.*88C>A
ENST00000423275.5:c.*1712C>A (RAF1)	ENSP00000401088.1:n.*1712C>A
ENST00000432427.2:c.1672C>A (RAF1)	ENSP00000398591.2:n.1672C>A
ENST00000442415.6:c.*88C>A (RAF1)	ENSP00000401888.2:n.*88C>A
ENST00000471449.1:n.724C>A (RAF1)
NM_002880.3:c.*88C>A , LRG_413t1:c.*88C>A (RAF1)	NP_002871.1:n.*88C>A
XM_005265355.1:c.*88C>A (RAF1)	XP_005265412.1:n.*88C>A
XM_005265357.1:c.*88C>A (RAF1)	XP_005265414.1:n.*88C>A
XM_005265358.3:c.*88C>A (RAF1)	XP_005265415.1:n.*88C>A
XM_005265359.3:c.*88C>A (RAF1)	XP_005265416.1:n.*88C>A
XM_011533974.1:c.*88C>A (RAF1)	XP_011532276.1:n.*88C>A
XM_011533975.1:c.*88C>A (RAF1)	XP_011532277.1:n.*88C>A
NM_001354689.1:c.*88C>A (RAF1)	NP_001341618.1:n.*88C>A
NM_001354690.1:c.*88C>A (RAF1)	NP_001341619.1:n.*88C>A
NM_001354691.1:c.*88C>A (RAF1)	NP_001341620.1:n.*88C>A
NM_001354692.1:c.*88C>A (RAF1)	NP_001341621.1:n.*88C>A
NM_001354693.1:c.*88C>A (RAF1)	NP_001341622.1:n.*88C>A
NM_001354694.1:c.*88C>A (RAF1)	NP_001341623.1:n.*88C>A
NM_001354695.1:c.*88C>A (RAF1)	NP_001341624.1:n.*88C>A
NR_148940.1:n.2563C>A (RAF1)
NR_148941.1:n.2509C>A (RAF1)
NR_148942.1:n.2448C>A (RAF1)
XM_011533974.3:c.*88C>A (RAF1)	XP_011532276.1:n.*88C>A
XM_017006966.1:c.*88C>A (RAF1)	XP_016862455.1:n.*88C>A
NM_001354689.3:c.*88C>A (RAF1)	NP_001341618.1:n.*88C>A
NM_001354690.2:c.*88C>A (RAF1)	NP_001341619.1:n.*88C>A
NM_001354691.2:c.*88C>A (RAF1)	NP_001341620.1:n.*88C>A
NM_001354692.2:c.*88C>A (RAF1)	NP_001341621.1:n.*88C>A
NM_001354693.2:c.*88C>A (RAF1)	NP_001341622.1:n.*88C>A
NM_001354694.2:c.*88C>A (RAF1)	NP_001341623.1:n.*88C>A
NM_001354695.2:c.*88C>A (RAF1)	NP_001341624.1:n.*88C>A
NR_148940.2:n.2479C>A (RAF1)
NR_148941.2:n.2425C>A (RAF1)
NR_148942.2:n.2364C>A (RAF1)
NM_001354690.3:c.*88C>A (RAF1)	NP_001341619.1:n.*88C>A
NM_001354691.3:c.*88C>A (RAF1)	NP_001341620.1:n.*88C>A
NM_001354692.3:c.*88C>A (RAF1)	NP_001341621.1:n.*88C>A
NM_001354693.3:c.*88C>A (RAF1)	NP_001341622.1:n.*88C>A
NM_001354694.3:c.*88C>A (RAF1)	NP_001341623.1:n.*88C>A
NM_001354695.3:c.*88C>A (RAF1)	NP_001341624.1:n.*88C>A
NM_002880.4:c.*88C>A (RAF1) MANE Select	NP_002871.1:n.*88C>A
NR_148940.3:n.2479C>A (RAF1)
NR_148941.3:n.2425C>A (RAF1)
NR_148942.3:n.2364C>A (RAF1)