Canonical Allele Identifier: CA351691140
Gene: SETD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475565A>C , CM000665.2:g.9475565A>C GRCh38
NC_000003.11:g.9517249A>C , CM000665.1:g.9517249A>C GRCh37
NC_000003.10:g.9492249A>C NCBI36
NG_034132.1:g.82866A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2758A>C
ENST00000682536.1:c.3899A>C ENSP00000507956.1:p.Gln1300Pro
ENST00000687014.1:n.4792A>C
ENST00000689167.1:n.2183A>C
ENST00000691925.1:n.6600A>C
ENST00000693430.1:n.6045A>C
ENST00000402198.7:c.3803A>C MANE Select ENSP00000385852.2:p.Gln1268Pro
ENST00000663774.1:c.*3949A>C ENSP00000499452.1:n.*3949A>C
ENST00000665872.1:c.*3872A>C ENSP00000499600.1:n.*3872A>C
ENST00000666307.1:c.*4177A>C ENSP00000499402.1:n.*4177A>C
ENST00000670063.1:c.*3908A>C ENSP00000499725.1:n.*3908A>C
ENST00000302463.10:c.3509A>C ENSP00000302028.6:p.Gln1170Pro
ENST00000399686.6:c.2722+409A>C
ENST00000402198.5:c.3803A>C ENSP00000385852.1:p.Gln1268Pro
ENST00000406341.5:c.3803A>C ENSP00000383939.1:p.Gln1268Pro
ENST00000407969.5:c.3860A>C ENSP00000384114.1:p.Gln1287Pro
ENST00000413704.5:c.2839A>C
ENST00000459941.1:n.934A>C
ENST00000466242.5:n.3144A>C
ENST00000466826.1:n.190A>C
ENST00000493918.5:n.3967A>C
NM_001080517.2:c.3803A>C NP_001073986.1:p.Gln1268Pro
NM_001292043.1:c.3509A>C NP_001278972.1:p.Gln1170Pro
XM_005265301.1:c.3860A>C XP_005265358.1:p.Gln1287Pro
XM_005265303.1:c.3803A>C XP_005265360.1:p.Gln1268Pro
XM_011533920.1:c.3977A>C XP_011532222.1:p.Gln1326Pro
XM_011533921.1:c.3977A>C XP_011532223.1:p.Gln1326Pro
XM_011533922.1:c.3956A>C XP_011532224.1:p.Gln1319Pro
XM_011533923.1:c.3956A>C XP_011532225.1:p.Gln1319Pro
XM_011533924.1:c.3956A>C XP_011532226.1:p.Gln1319Pro
XM_011533925.1:c.3938A>C XP_011532227.1:p.Gln1313Pro
XM_011533926.1:c.3920A>C XP_011532228.1:p.Gln1307Pro
XM_011533927.1:c.3920A>C XP_011532229.1:p.Gln1307Pro
XM_011533928.1:c.3899A>C XP_011532230.1:p.Gln1300Pro
XM_011533929.1:c.3881A>C XP_011532231.1:p.Gln1294Pro
XM_011533930.1:c.3842A>C XP_011532232.1:p.Gln1281Pro
XM_011533931.1:c.3566A>C XP_011532233.1:p.Gln1189Pro
XM_011533932.1:c.3527A>C XP_011532234.1:p.Gln1176Pro
XM_011533933.1:c.3527A>C XP_011532235.1:p.Gln1176Pro
NM_001349451.1:c.3509A>C NP_001336380.1:p.Gln1170Pro
XM_011533921.2:c.3977A>C XP_011532223.1:p.Gln1326Pro
XM_017006767.1:c.3977A>C XP_016862256.1:p.Gln1326Pro
XM_017006768.2:c.3956A>C XP_016862257.1:p.Gln1319Pro
XM_017006770.1:c.3920A>C XP_016862259.1:p.Gln1307Pro
XM_017006771.1:c.3917A>C XP_016862260.1:p.Gln1306Pro
XM_017006772.1:c.3881A>C XP_016862261.1:p.Gln1294Pro
XM_017006773.1:c.3881A>C XP_016862262.1:p.Gln1294Pro
XM_017006774.1:c.3860A>C XP_016862263.1:p.Gln1287Pro
XM_017006775.1:c.3824A>C XP_016862264.1:p.Gln1275Pro
XM_017006776.1:c.3566A>C XP_016862265.1:p.Gln1189Pro
XM_017006777.1:c.3566A>C XP_016862266.1:p.Gln1189Pro
XM_017006778.1:c.3566A>C XP_016862267.1:p.Gln1189Pro
XM_017006779.1:c.3527A>C XP_016862268.1:p.Gln1176Pro
XM_017006780.1:c.3527A>C XP_016862269.1:p.Gln1176Pro
XM_017006783.1:c.3299A>C XP_016862272.1:p.Gln1100Pro
XM_024453620.1:c.3938A>C XP_024309388.1:p.Gln1313Pro
XM_024453621.1:c.3614A>C XP_024309389.1:p.Gln1205Pro
XR_001740195.2:n.8186A>C
NM_001080517.3:c.3803A>C MANE Select NP_001073986.1:p.Gln1268Pro
NM_001292043.2:c.3509A>C NP_001278972.1:p.Gln1170Pro
NM_001349451.2:c.3509A>C NP_001336380.1:p.Gln1170Pro