Canonical Allele Identifier: CA351692059
Gene: SETD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475652C>A , CM000665.2:g.9475652C>A GRCh38
NC_000003.11:g.9517336C>A , CM000665.1:g.9517336C>A GRCh37
NC_000003.10:g.9492336C>A NCBI36
NG_034132.1:g.82953C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2845C>A
ENST00000682536.1:c.3986C>A ENSP00000507956.1:p.Thr1329Lys
ENST00000687014.1:n.4879C>A
ENST00000689167.1:n.2270C>A
ENST00000691925.1:n.6687C>A
ENST00000693430.1:n.6132C>A
ENST00000402198.7:c.3890C>A MANE Select ENSP00000385852.2:p.Thr1297Lys
ENST00000663774.1:c.*4036C>A ENSP00000499452.1:n.*4036C>A
ENST00000665872.1:c.*3959C>A ENSP00000499600.1:n.*3959C>A
ENST00000666307.1:c.*4264C>A ENSP00000499402.1:n.*4264C>A
ENST00000670063.1:c.*3995C>A ENSP00000499725.1:n.*3995C>A
ENST00000302463.10:c.3596C>A ENSP00000302028.6:p.Thr1199Lys
ENST00000399686.6:c.2722+496C>A
ENST00000402198.5:c.3890C>A ENSP00000385852.1:p.Thr1297Lys
ENST00000406341.5:c.3890C>A ENSP00000383939.1:p.Thr1297Lys
ENST00000407969.5:c.3947C>A ENSP00000384114.1:p.Thr1316Lys
ENST00000413704.5:c.2926C>A
ENST00000459941.1:n.1021C>A
ENST00000466242.5:n.3231C>A
ENST00000466826.1:n.277C>A
ENST00000493918.5:n.4054C>A
NM_001080517.2:c.3890C>A NP_001073986.1:p.Thr1297Lys
NM_001292043.1:c.3596C>A NP_001278972.1:p.Thr1199Lys
XM_005265301.1:c.3947C>A XP_005265358.1:p.Thr1316Lys
XM_005265303.1:c.3890C>A XP_005265360.1:p.Thr1297Lys
XM_011533920.1:c.4064C>A XP_011532222.1:p.Thr1355Lys
XM_011533921.1:c.4064C>A XP_011532223.1:p.Thr1355Lys
XM_011533922.1:c.4043C>A XP_011532224.1:p.Thr1348Lys
XM_011533923.1:c.4043C>A XP_011532225.1:p.Thr1348Lys
XM_011533924.1:c.4043C>A XP_011532226.1:p.Thr1348Lys
XM_011533925.1:c.4025C>A XP_011532227.1:p.Thr1342Lys
XM_011533926.1:c.4007C>A XP_011532228.1:p.Thr1336Lys
XM_011533927.1:c.4007C>A XP_011532229.1:p.Thr1336Lys
XM_011533928.1:c.3986C>A XP_011532230.1:p.Thr1329Lys
XM_011533929.1:c.3968C>A XP_011532231.1:p.Thr1323Lys
XM_011533930.1:c.3929C>A XP_011532232.1:p.Thr1310Lys
XM_011533931.1:c.3653C>A XP_011532233.1:p.Thr1218Lys
XM_011533932.1:c.3614C>A XP_011532234.1:p.Thr1205Lys
XM_011533933.1:c.3614C>A XP_011532235.1:p.Thr1205Lys
NM_001349451.1:c.3596C>A NP_001336380.1:p.Thr1199Lys
XM_011533921.2:c.4064C>A XP_011532223.1:p.Thr1355Lys
XM_017006767.1:c.4064C>A XP_016862256.1:p.Thr1355Lys
XM_017006768.2:c.4043C>A XP_016862257.1:p.Thr1348Lys
XM_017006770.1:c.4007C>A XP_016862259.1:p.Thr1336Lys
XM_017006771.1:c.4004C>A XP_016862260.1:p.Thr1335Lys
XM_017006772.1:c.3968C>A XP_016862261.1:p.Thr1323Lys
XM_017006773.1:c.3968C>A XP_016862262.1:p.Thr1323Lys
XM_017006774.1:c.3947C>A XP_016862263.1:p.Thr1316Lys
XM_017006775.1:c.3911C>A XP_016862264.1:p.Thr1304Lys
XM_017006776.1:c.3653C>A XP_016862265.1:p.Thr1218Lys
XM_017006777.1:c.3653C>A XP_016862266.1:p.Thr1218Lys
XM_017006778.1:c.3653C>A XP_016862267.1:p.Thr1218Lys
XM_017006779.1:c.3614C>A XP_016862268.1:p.Thr1205Lys
XM_017006780.1:c.3614C>A XP_016862269.1:p.Thr1205Lys
XM_017006783.1:c.3386C>A XP_016862272.1:p.Thr1129Lys
XM_024453620.1:c.4025C>A XP_024309388.1:p.Thr1342Lys
XM_024453621.1:c.3701C>A XP_024309389.1:p.Thr1234Lys
XR_001740195.2:n.8273C>A
NM_001080517.3:c.3890C>A MANE Select NP_001073986.1:p.Thr1297Lys
NM_001292043.2:c.3596C>A NP_001278972.1:p.Thr1199Lys
NM_001349451.2:c.3596C>A NP_001336380.1:p.Thr1199Lys