Canonical Allele Identifier: CA1344742379
Gene: SETD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475544C= , CM000665.2:g.9475544C= GRCh38
NC_000003.11:g.9517228C= , CM000665.1:g.9517228C= GRCh37
NC_000003.10:g.9492228C= NCBI36
NG_034132.1:g.82845C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2737C=
ENST00000682536.1:c.3878C= ENSP00000507956.1:p.Pro1293=
ENST00000687014.1:n.4771C=
ENST00000689167.1:n.2162C=
ENST00000691925.1:n.6579C=
ENST00000693430.1:n.6024C=
ENST00000402198.7:c.3782C= MANE Select ENSP00000385852.2:p.Pro1261=
ENST00000663774.1:c.*3928C= ENSP00000499452.1:n.*3928C=
ENST00000665872.1:c.*3851C= ENSP00000499600.1:n.*3851C=
ENST00000666307.1:c.*4156C= ENSP00000499402.1:n.*4156C=
ENST00000670063.1:c.*3887C= ENSP00000499725.1:n.*3887C=
ENST00000302463.10:c.3488C= ENSP00000302028.6:p.Pro1163=
ENST00000399686.6:c.2722+388C=
ENST00000402198.5:c.3782C= ENSP00000385852.1:p.Pro1261=
ENST00000406341.5:c.3782C= ENSP00000383939.1:p.Pro1261=
ENST00000407969.5:c.3839C= ENSP00000384114.1:p.Pro1280=
ENST00000413704.5:c.2818C=
ENST00000459941.1:n.913C=
ENST00000466242.5:n.3123C=
ENST00000466826.1:n.169C=
ENST00000493918.5:n.3946C=
NM_001080517.2:c.3782C= NP_001073986.1:p.Pro1261=
NM_001292043.1:c.3488C= NP_001278972.1:p.Pro1163=
XM_005265301.1:c.3839C= XP_005265358.1:p.Pro1280=
XM_005265303.1:c.3782C= XP_005265360.1:p.Pro1261=
XM_011533920.1:c.3956C= XP_011532222.1:p.Pro1319=
XM_011533921.1:c.3956C= XP_011532223.1:p.Pro1319=
XM_011533922.1:c.3935C= XP_011532224.1:p.Pro1312=
XM_011533923.1:c.3935C= XP_011532225.1:p.Pro1312=
XM_011533924.1:c.3935C= XP_011532226.1:p.Pro1312=
XM_011533925.1:c.3917C= XP_011532227.1:p.Pro1306=
XM_011533926.1:c.3899C= XP_011532228.1:p.Pro1300=
XM_011533927.1:c.3899C= XP_011532229.1:p.Pro1300=
XM_011533928.1:c.3878C= XP_011532230.1:p.Pro1293=
XM_011533929.1:c.3860C= XP_011532231.1:p.Pro1287=
XM_011533930.1:c.3821C= XP_011532232.1:p.Pro1274=
XM_011533931.1:c.3545C= XP_011532233.1:p.Pro1182=
XM_011533932.1:c.3506C= XP_011532234.1:p.Pro1169=
XM_011533933.1:c.3506C= XP_011532235.1:p.Pro1169=
NM_001349451.1:c.3488C= NP_001336380.1:p.Pro1163=
XM_011533921.2:c.3956C= XP_011532223.1:p.Pro1319=
XM_017006767.1:c.3956C= XP_016862256.1:p.Pro1319=
XM_017006768.2:c.3935C= XP_016862257.1:p.Pro1312=
XM_017006770.1:c.3899C= XP_016862259.1:p.Pro1300=
XM_017006771.1:c.3896C= XP_016862260.1:p.Pro1299=
XM_017006772.1:c.3860C= XP_016862261.1:p.Pro1287=
XM_017006773.1:c.3860C= XP_016862262.1:p.Pro1287=
XM_017006774.1:c.3839C= XP_016862263.1:p.Pro1280=
XM_017006775.1:c.3803C= XP_016862264.1:p.Pro1268=
XM_017006776.1:c.3545C= XP_016862265.1:p.Pro1182=
XM_017006777.1:c.3545C= XP_016862266.1:p.Pro1182=
XM_017006778.1:c.3545C= XP_016862267.1:p.Pro1182=
XM_017006779.1:c.3506C= XP_016862268.1:p.Pro1169=
XM_017006780.1:c.3506C= XP_016862269.1:p.Pro1169=
XM_017006783.1:c.3278C= XP_016862272.1:p.Pro1093=
XM_024453620.1:c.3917C= XP_024309388.1:p.Pro1306=
XM_024453621.1:c.3593C= XP_024309389.1:p.Pro1198=
XR_001740195.2:n.8165C=
NM_001080517.3:c.3782C= MANE Select NP_001073986.1:p.Pro1261=
NM_001292043.2:c.3488C= NP_001278972.1:p.Pro1163=
NM_001349451.2:c.3488C= NP_001336380.1:p.Pro1163=