Canonical Allele Identifier: CA351691322
Gene: SETD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475583A>C , CM000665.2:g.9475583A>C GRCh38
NC_000003.11:g.9517267A>C , CM000665.1:g.9517267A>C GRCh37
NC_000003.10:g.9492267A>C NCBI36
NG_034132.1:g.82884A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2776A>C
ENST00000682536.1:c.3917A>C ENSP00000507956.1:p.Tyr1306Ser
ENST00000687014.1:n.4810A>C
ENST00000689167.1:n.2201A>C
ENST00000691925.1:n.6618A>C
ENST00000693430.1:n.6063A>C
ENST00000402198.7:c.3821A>C MANE Select ENSP00000385852.2:p.Tyr1274Ser
ENST00000663774.1:c.*3967A>C ENSP00000499452.1:n.*3967A>C
ENST00000665872.1:c.*3890A>C ENSP00000499600.1:n.*3890A>C
ENST00000666307.1:c.*4195A>C ENSP00000499402.1:n.*4195A>C
ENST00000670063.1:c.*3926A>C ENSP00000499725.1:n.*3926A>C
ENST00000302463.10:c.3527A>C ENSP00000302028.6:p.Tyr1176Ser
ENST00000399686.6:c.2722+427A>C
ENST00000402198.5:c.3821A>C ENSP00000385852.1:p.Tyr1274Ser
ENST00000406341.5:c.3821A>C ENSP00000383939.1:p.Tyr1274Ser
ENST00000407969.5:c.3878A>C ENSP00000384114.1:p.Tyr1293Ser
ENST00000413704.5:c.2857A>C
ENST00000459941.1:n.952A>C
ENST00000466242.5:n.3162A>C
ENST00000466826.1:n.208A>C
ENST00000493918.5:n.3985A>C
NM_001080517.2:c.3821A>C NP_001073986.1:p.Tyr1274Ser
NM_001292043.1:c.3527A>C NP_001278972.1:p.Tyr1176Ser
XM_005265301.1:c.3878A>C XP_005265358.1:p.Tyr1293Ser
XM_005265303.1:c.3821A>C XP_005265360.1:p.Tyr1274Ser
XM_011533920.1:c.3995A>C XP_011532222.1:p.Tyr1332Ser
XM_011533921.1:c.3995A>C XP_011532223.1:p.Tyr1332Ser
XM_011533922.1:c.3974A>C XP_011532224.1:p.Tyr1325Ser
XM_011533923.1:c.3974A>C XP_011532225.1:p.Tyr1325Ser
XM_011533924.1:c.3974A>C XP_011532226.1:p.Tyr1325Ser
XM_011533925.1:c.3956A>C XP_011532227.1:p.Tyr1319Ser
XM_011533926.1:c.3938A>C XP_011532228.1:p.Tyr1313Ser
XM_011533927.1:c.3938A>C XP_011532229.1:p.Tyr1313Ser
XM_011533928.1:c.3917A>C XP_011532230.1:p.Tyr1306Ser
XM_011533929.1:c.3899A>C XP_011532231.1:p.Tyr1300Ser
XM_011533930.1:c.3860A>C XP_011532232.1:p.Tyr1287Ser
XM_011533931.1:c.3584A>C XP_011532233.1:p.Tyr1195Ser
XM_011533932.1:c.3545A>C XP_011532234.1:p.Tyr1182Ser
XM_011533933.1:c.3545A>C XP_011532235.1:p.Tyr1182Ser
NM_001349451.1:c.3527A>C NP_001336380.1:p.Tyr1176Ser
XM_011533921.2:c.3995A>C XP_011532223.1:p.Tyr1332Ser
XM_017006767.1:c.3995A>C XP_016862256.1:p.Tyr1332Ser
XM_017006768.2:c.3974A>C XP_016862257.1:p.Tyr1325Ser
XM_017006770.1:c.3938A>C XP_016862259.1:p.Tyr1313Ser
XM_017006771.1:c.3935A>C XP_016862260.1:p.Tyr1312Ser
XM_017006772.1:c.3899A>C XP_016862261.1:p.Tyr1300Ser
XM_017006773.1:c.3899A>C XP_016862262.1:p.Tyr1300Ser
XM_017006774.1:c.3878A>C XP_016862263.1:p.Tyr1293Ser
XM_017006775.1:c.3842A>C XP_016862264.1:p.Tyr1281Ser
XM_017006776.1:c.3584A>C XP_016862265.1:p.Tyr1195Ser
XM_017006777.1:c.3584A>C XP_016862266.1:p.Tyr1195Ser
XM_017006778.1:c.3584A>C XP_016862267.1:p.Tyr1195Ser
XM_017006779.1:c.3545A>C XP_016862268.1:p.Tyr1182Ser
XM_017006780.1:c.3545A>C XP_016862269.1:p.Tyr1182Ser
XM_017006783.1:c.3317A>C XP_016862272.1:p.Tyr1106Ser
XM_024453620.1:c.3956A>C XP_024309388.1:p.Tyr1319Ser
XM_024453621.1:c.3632A>C XP_024309389.1:p.Tyr1211Ser
XR_001740195.2:n.8204A>C
NM_001080517.3:c.3821A>C MANE Select NP_001073986.1:p.Tyr1274Ser
NM_001292043.2:c.3527A>C NP_001278972.1:p.Tyr1176Ser
NM_001349451.2:c.3527A>C NP_001336380.1:p.Tyr1176Ser