Canonical Allele Identifier: CA351509254
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600245A>C , CM000665.2:g.12600245A>C GRCh38
NC_000003.11:g.12641744A>C , CM000665.1:g.12641744A>C GRCh37
NC_000003.10:g.12616744A>C NCBI36
NG_007467.1:g.68935T>G , LRG_413:g.68935T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*562T>G ENSP00000401088.1:n.*562T>G
ENST00000432427.3:c.217T>G
ENST00000465826.6:n.488T>G
ENST00000491290.2:n.1274T>G
ENST00000684903.1:c.*574T>G ENSP00000508612.1:n.*574T>G
ENST00000685348.1:c.*574T>G ENSP00000510285.1:n.*574T>G
ENST00000685437.1:c.798T>G ENSP00000508794.1:p.Asn266Lys
ENST00000685438.1:n.661T>G
ENST00000685653.1:c.897T>G ENSP00000509968.1:p.Asn299Lys
ENST00000685738.1:c.897T>G ENSP00000510156.1:p.Asn299Lys
ENST00000686409.1:n.1605T>G
ENST00000686455.1:n.1260T>G
ENST00000686479.1:n.1268T>G
ENST00000686762.1:c.897T>G ENSP00000509767.1:p.Asn299Lys
ENST00000687257.1:n.1133T>G
ENST00000687326.1:c.897T>G ENSP00000509665.1:p.Asn299Lys
ENST00000687486.1:c.182+143T>G
ENST00000687505.1:n.1015T>G
ENST00000687923.1:c.798T>G ENSP00000510255.1:p.Asn266Lys
ENST00000687940.1:n.1274T>G
ENST00000688269.1:n.1493T>G
ENST00000688326.1:c.217T>G
ENST00000688444.1:n.1223T>G
ENST00000688543.1:c.798T>G ENSP00000509612.1:p.Asn266Lys
ENST00000688625.1:c.*475T>G ENSP00000509522.1:n.*475T>G
ENST00000688803.1:n.1128T>G
ENST00000689097.1:c.*574T>G ENSP00000509756.1:n.*574T>G
ENST00000689389.1:c.897T>G ENSP00000510213.1:p.Asn299Lys
ENST00000689418.1:c.*574T>G ENSP00000509467.1:n.*574T>G
ENST00000689481.1:c.*574T>G ENSP00000510248.1:n.*574T>G
ENST00000689540.1:n.1047T>G
ENST00000689876.1:c.897T>G ENSP00000508535.1:p.Asn299Lys
ENST00000689914.1:c.897T>G ENSP00000509847.1:p.Asn299Lys
ENST00000690397.1:c.786T>G ENSP00000508730.1:p.Asn262Lys
ENST00000690460.1:c.885T>G ENSP00000509106.1:p.Asn295Lys
ENST00000690625.1:n.1200T>G
ENST00000691268.1:c.324T>G
ENST00000691396.1:c.*690T>G ENSP00000510712.1:n.*690T>G
ENST00000691724.1:c.897T>G ENSP00000509255.1:p.Asn299Lys
ENST00000691779.1:c.*475T>G ENSP00000508592.1:n.*475T>G
ENST00000691899.1:c.897T>G ENSP00000508763.1:p.Asn299Lys
ENST00000692069.1:n.1120T>G
ENST00000692093.1:c.798T>G ENSP00000509669.1:p.Asn266Lys
ENST00000692311.1:n.1378T>G
ENST00000692558.1:n.1262T>G
ENST00000692773.1:c.*634T>G ENSP00000509055.1:n.*634T>G
ENST00000692830.1:c.*642T>G ENSP00000509461.1:n.*642T>G
ENST00000693069.1:c.798T>G ENSP00000510072.1:p.Asn266Lys
ENST00000693312.1:c.672T>G ENSP00000508686.1:p.Asn224Lys
ENST00000693664.1:c.897T>G ENSP00000509614.1:p.Asn299Lys
ENST00000693705.1:c.*574T>G ENSP00000510697.1:n.*574T>G
ENST00000251849.9:c.897T>G MANE Select ENSP00000251849.4:p.Asn299Lys
ENST00000442415.7:c.957T>G ENSP00000401888.2:p.Asn319Lys
ENST00000251849.8:c.897T>G ENSP00000251849.4:p.Asn299Lys
ENST00000423275.5:c.*574T>G ENSP00000401088.1:n.*574T>G
ENST00000432427.2:c.534T>G ENSP00000398591.2:p.Asn178Lys
ENST00000442415.6:c.957T>G ENSP00000401888.2:p.Asn319Lys
ENST00000465826.5:n.141T>G
ENST00000491290.1:n.526T>G
NM_002880.3:c.897T>G , LRG_413t1:c.897T>G NP_002871.1:p.Asn299Lys
XM_005265355.1:c.897T>G XP_005265412.1:p.Asn299Lys
XM_005265357.1:c.798T>G XP_005265414.1:p.Asn266Lys
XM_005265358.3:c.654T>G XP_005265415.1:p.Asn218Lys
XM_005265359.3:c.555T>G XP_005265416.1:p.Asn185Lys
XM_005265360.1:c.897T>G XP_005265417.1:p.Asn299Lys
XM_011533974.1:c.897T>G XP_011532276.1:p.Asn299Lys
XM_011533975.1:c.654T>G XP_011532277.1:p.Asn218Lys
NM_001354689.1:c.957T>G NP_001341618.1:p.Asn319Lys
NM_001354690.1:c.897T>G NP_001341619.1:p.Asn299Lys
NM_001354691.1:c.654T>G NP_001341620.1:p.Asn218Lys
NM_001354692.1:c.654T>G NP_001341621.1:p.Asn218Lys
NM_001354693.1:c.798T>G NP_001341622.1:p.Asn266Lys
NM_001354694.1:c.714T>G NP_001341623.1:p.Asn238Lys
NM_001354695.1:c.555T>G NP_001341624.1:p.Asn185Lys
NR_148940.1:n.1312T>G
NR_148941.1:n.1312T>G
NR_148942.1:n.1312T>G
XM_011533974.3:c.897T>G XP_011532276.1:p.Asn299Lys
XM_017006966.1:c.798T>G XP_016862455.1:p.Asn266Lys
XR_001740227.1:n.1129T>G
NM_001354689.3:c.957T>G NP_001341618.1:p.Asn319Lys
NM_001354690.2:c.897T>G NP_001341619.1:p.Asn299Lys
NM_001354691.2:c.654T>G NP_001341620.1:p.Asn218Lys
NM_001354692.2:c.654T>G NP_001341621.1:p.Asn218Lys
NM_001354693.2:c.798T>G NP_001341622.1:p.Asn266Lys
NM_001354694.2:c.714T>G NP_001341623.1:p.Asn238Lys
NM_001354695.2:c.555T>G NP_001341624.1:p.Asn185Lys
NR_148940.2:n.1228T>G
NR_148941.2:n.1228T>G
NR_148942.2:n.1228T>G
NM_001354690.3:c.897T>G NP_001341619.1:p.Asn299Lys
NM_001354691.3:c.654T>G NP_001341620.1:p.Asn218Lys
NM_001354692.3:c.654T>G NP_001341621.1:p.Asn218Lys
NM_001354693.3:c.798T>G NP_001341622.1:p.Asn266Lys
NM_001354694.3:c.714T>G NP_001341623.1:p.Asn238Lys
NM_001354695.3:c.555T>G NP_001341624.1:p.Asn185Lys
NM_002880.4:c.897T>G MANE Select NP_002871.1:p.Asn299Lys
NR_148940.3:n.1228T>G
NR_148941.3:n.1228T>G
NR_148942.3:n.1228T>G