Canonical Allele Identifier: CA2664506640

Linked Data

gnomAD v4: 3-12584339-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584339C>A , CM000665.2:g.12584339C>A GRCh38
NC_000003.11:g.12625838C>A , CM000665.1:g.12625838C>A GRCh37
NC_000003.10:g.12600838C>A NCBI36
NG_007467.1:g.84841G>T , LRG_413:g.84841G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1787G>T (RAF1) ENSP00000401088.1:n.*1787G>T
ENST00000432427.3:c.1439G>T (RAF1)
ENST00000460610.2:n.6434G>T (RAF1)
ENST00000471449.2:n.932G>T (RAF1)
ENST00000475353.2:n.4402G>T (RAF1)
ENST00000684903.1:c.*1799G>T (RAF1) ENSP00000508612.1:n.*1799G>T
ENST00000685348.1:c.*1833G>T (RAF1) ENSP00000510285.1:n.*1833G>T
ENST00000685437.1:c.*175G>T (RAF1) ENSP00000508794.1:n.*175G>T
ENST00000685653.1:c.*175G>T (RAF1) ENSP00000509968.1:n.*175G>T
ENST00000685697.1:n.2857G>T (RAF1)
ENST00000685738.1:c.*1086G>T (RAF1) ENSP00000510156.1:n.*1086G>T
ENST00000686409.1:n.5531G>T (RAF1)
ENST00000686455.1:n.4843G>T (RAF1)
ENST00000686762.1:c.*681G>T (RAF1) ENSP00000509767.1:n.*681G>T
ENST00000687257.1:n.4576G>T (RAF1)
ENST00000687326.1:c.*3414G>T (RAF1) ENSP00000509665.1:n.*3414G>T
ENST00000687505.1:n.2240G>T (RAF1)
ENST00000687923.1:c.*175G>T (RAF1) ENSP00000510255.1:n.*175G>T
ENST00000688269.1:n.2718G>T (RAF1)
ENST00000688444.1:n.4239G>T (RAF1)
ENST00000688543.1:c.*175G>T (RAF1) ENSP00000509612.1:n.*175G>T
ENST00000688625.1:c.*3491G>T (RAF1) ENSP00000509522.1:n.*3491G>T
ENST00000688803.1:n.3550G>T (RAF1)
ENST00000689097.1:c.*1799G>T (RAF1) ENSP00000509756.1:n.*1799G>T
ENST00000689389.1:c.*175G>T (RAF1) ENSP00000510213.1:n.*175G>T
ENST00000689418.1:c.*4017G>T (RAF1) ENSP00000509467.1:n.*4017G>T
ENST00000689540.1:n.4490G>T (RAF1)
ENST00000689876.1:c.*671G>T (RAF1) ENSP00000508535.1:n.*671G>T
ENST00000689914.1:c.*1056G>T (RAF1) ENSP00000509847.1:n.*1056G>T
ENST00000690397.1:c.*175G>T (RAF1) ENSP00000508730.1:n.*175G>T
ENST00000690460.1:c.*175G>T (RAF1) ENSP00000509106.1:n.*175G>T
ENST00000690585.1:c.848G>T (RAF1)
ENST00000690625.1:n.3158G>T (RAF1)
ENST00000691396.1:c.*1994G>T (RAF1) ENSP00000510712.1:n.*1994G>T
ENST00000691643.1:n.3175G>T (RAF1)
ENST00000691724.1:c.*1079G>T (RAF1) ENSP00000509255.1:n.*1079G>T
ENST00000691779.1:c.*1700G>T (RAF1) ENSP00000508592.1:n.*1700G>T
ENST00000691888.1:c.996G>T (RAF1)
ENST00000691899.1:c.*175G>T (RAF1) ENSP00000508763.1:n.*175G>T
ENST00000692069.1:n.5046G>T (RAF1)
ENST00000692093.1:c.*175G>T (RAF1) ENSP00000509669.1:n.*175G>T
ENST00000692311.1:n.2946G>T (RAF1)
ENST00000692558.1:n.4705G>T (RAF1)
ENST00000692773.1:c.*1859G>T (RAF1) ENSP00000509055.1:n.*1859G>T
ENST00000692830.1:c.*1867G>T (RAF1) ENSP00000509461.1:n.*1867G>T
ENST00000693312.1:c.*175G>T (RAF1) ENSP00000508686.1:n.*175G>T
ENST00000693664.1:c.*573G>T (RAF1) ENSP00000509614.1:n.*573G>T
ENST00000693705.1:c.*1501G>T (RAF1) ENSP00000510697.1:n.*1501G>T
ENST00000251849.9:c.*175G>T (RAF1) MANE Select ENSP00000251849.4:n.*175G>T
ENST00000442415.7:c.*175G>T (RAF1) ENSP00000401888.2:n.*175G>T
ENST00000676541.1:c.*2086C>A (MKRN2) ENSP00000503730.1:n.*2086C>A
ENST00000677142.1:c.*2086C>A (MKRN2) ENSP00000504455.1:n.*2086C>A
ENST00000677816.1:c.*641C>A (MKRN2) ENSP00000502893.1:n.*641C>A
ENST00000677941.1:n.2149C>A (MKRN2)
ENST00000251849.8:c.*175G>T (RAF1) ENSP00000251849.4:n.*175G>T
ENST00000423275.5:c.*1799G>T (RAF1) ENSP00000401088.1:n.*1799G>T
ENST00000432427.2:c.1759G>T (RAF1) ENSP00000398591.2:n.1759G>T
ENST00000442415.6:c.*175G>T (RAF1) ENSP00000401888.2:n.*175G>T
NM_002880.3:c.*175G>T , LRG_413t1:c.*175G>T (RAF1) NP_002871.1:n.*175G>T
XM_005265355.1:c.*175G>T (RAF1) XP_005265412.1:n.*175G>T
XM_005265357.1:c.*175G>T (RAF1) XP_005265414.1:n.*175G>T
XM_005265358.3:c.*175G>T (RAF1) XP_005265415.1:n.*175G>T
XM_005265359.3:c.*175G>T (RAF1) XP_005265416.1:n.*175G>T
XM_011533974.1:c.*175G>T (RAF1) XP_011532276.1:n.*175G>T
XM_011533975.1:c.*175G>T (RAF1) XP_011532277.1:n.*175G>T
NM_001354689.1:c.*175G>T (RAF1) NP_001341618.1:n.*175G>T
NM_001354690.1:c.*175G>T (RAF1) NP_001341619.1:n.*175G>T
NM_001354691.1:c.*175G>T (RAF1) NP_001341620.1:n.*175G>T
NM_001354692.1:c.*175G>T (RAF1) NP_001341621.1:n.*175G>T
NM_001354693.1:c.*175G>T (RAF1) NP_001341622.1:n.*175G>T
NM_001354694.1:c.*175G>T (RAF1) NP_001341623.1:n.*175G>T
NM_001354695.1:c.*175G>T (RAF1) NP_001341624.1:n.*175G>T
NR_148940.1:n.2650G>T (RAF1)
NR_148941.1:n.2596G>T (RAF1)
NR_148942.1:n.2535G>T (RAF1)
XM_011533974.3:c.*175G>T (RAF1) XP_011532276.1:n.*175G>T
XM_017006966.1:c.*175G>T (RAF1) XP_016862455.1:n.*175G>T
NM_001354689.3:c.*175G>T (RAF1) NP_001341618.1:n.*175G>T
NM_001354690.2:c.*175G>T (RAF1) NP_001341619.1:n.*175G>T
NM_001354691.2:c.*175G>T (RAF1) NP_001341620.1:n.*175G>T
NM_001354692.2:c.*175G>T (RAF1) NP_001341621.1:n.*175G>T
NM_001354693.2:c.*175G>T (RAF1) NP_001341622.1:n.*175G>T
NM_001354694.2:c.*175G>T (RAF1) NP_001341623.1:n.*175G>T
NM_001354695.2:c.*175G>T (RAF1) NP_001341624.1:n.*175G>T
NR_148940.2:n.2566G>T (RAF1)
NR_148941.2:n.2512G>T (RAF1)
NR_148942.2:n.2451G>T (RAF1)
NM_001354690.3:c.*175G>T (RAF1) NP_001341619.1:n.*175G>T
NM_001354691.3:c.*175G>T (RAF1) NP_001341620.1:n.*175G>T
NM_001354692.3:c.*175G>T (RAF1) NP_001341621.1:n.*175G>T
NM_001354693.3:c.*175G>T (RAF1) NP_001341622.1:n.*175G>T
NM_001354694.3:c.*175G>T (RAF1) NP_001341623.1:n.*175G>T
NM_001354695.3:c.*175G>T (RAF1) NP_001341624.1:n.*175G>T
NM_002880.4:c.*175G>T (RAF1) MANE Select NP_002871.1:n.*175G>T
NR_148940.3:n.2566G>T (RAF1)
NR_148941.3:n.2512G>T (RAF1)
NR_148942.3:n.2451G>T (RAF1)