Canonical Allele Identifier: CA1344742768
Gene: SETD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475737A= , CM000665.2:g.9475737A= GRCh38
NC_000003.11:g.9517421A= , CM000665.1:g.9517421A= GRCh37
NC_000003.10:g.9492421A= NCBI36
NG_034132.1:g.83038A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2930A=
ENST00000682536.1:c.4071A= ENSP00000507956.1:p.Pro1357=
ENST00000687014.1:n.4964A=
ENST00000689167.1:n.2355A=
ENST00000693430.1:n.6217A=
ENST00000402198.7:c.3975A= MANE Select ENSP00000385852.2:p.Pro1325=
ENST00000663774.1:c.*4121A= ENSP00000499452.1:n.*4121A=
ENST00000665872.1:c.*4044A= ENSP00000499600.1:n.*4044A=
ENST00000666307.1:c.*4349A= ENSP00000499402.1:n.*4349A=
ENST00000670063.1:c.*4080A= ENSP00000499725.1:n.*4080A=
ENST00000302463.10:c.3681A= ENSP00000302028.6:p.Pro1227=
ENST00000399686.6:c.2722+581A=
ENST00000402198.5:c.3975A= ENSP00000385852.1:p.Pro1325=
ENST00000406341.5:c.3975A= ENSP00000383939.1:p.Pro1325=
ENST00000407969.5:c.4032A= ENSP00000384114.1:p.Pro1344=
ENST00000413704.5:c.3011A=
ENST00000466242.5:n.3316A=
ENST00000493918.5:n.4139A=
NM_001080517.2:c.3975A= NP_001073986.1:p.Pro1325=
NM_001292043.1:c.3681A= NP_001278972.1:p.Pro1227=
XM_005265301.1:c.4032A= XP_005265358.1:p.Pro1344=
XM_005265303.1:c.3975A= XP_005265360.1:p.Pro1325=
XM_011533920.1:c.4149A= XP_011532222.1:p.Pro1383=
XM_011533921.1:c.4149A= XP_011532223.1:p.Pro1383=
XM_011533922.1:c.4128A= XP_011532224.1:p.Pro1376=
XM_011533923.1:c.4128A= XP_011532225.1:p.Pro1376=
XM_011533924.1:c.4128A= XP_011532226.1:p.Pro1376=
XM_011533925.1:c.4110A= XP_011532227.1:p.Pro1370=
XM_011533926.1:c.4092A= XP_011532228.1:p.Pro1364=
XM_011533927.1:c.4092A= XP_011532229.1:p.Pro1364=
XM_011533928.1:c.4071A= XP_011532230.1:p.Pro1357=
XM_011533929.1:c.4053A= XP_011532231.1:p.Pro1351=
XM_011533930.1:c.4014A= XP_011532232.1:p.Pro1338=
XM_011533931.1:c.3738A= XP_011532233.1:p.Pro1246=
XM_011533932.1:c.3699A= XP_011532234.1:p.Pro1233=
XM_011533933.1:c.3699A= XP_011532235.1:p.Pro1233=
NM_001349451.1:c.3681A= NP_001336380.1:p.Pro1227=
XM_011533921.2:c.4149A= XP_011532223.1:p.Pro1383=
XM_017006767.1:c.4149A= XP_016862256.1:p.Pro1383=
XM_017006768.2:c.4128A= XP_016862257.1:p.Pro1376=
XM_017006770.1:c.4092A= XP_016862259.1:p.Pro1364=
XM_017006771.1:c.4089A= XP_016862260.1:p.Pro1363=
XM_017006772.1:c.4053A= XP_016862261.1:p.Pro1351=
XM_017006773.1:c.4053A= XP_016862262.1:p.Pro1351=
XM_017006774.1:c.4032A= XP_016862263.1:p.Pro1344=
XM_017006775.1:c.3996A= XP_016862264.1:p.Pro1332=
XM_017006776.1:c.3738A= XP_016862265.1:p.Pro1246=
XM_017006777.1:c.3738A= XP_016862266.1:p.Pro1246=
XM_017006778.1:c.3738A= XP_016862267.1:p.Pro1246=
XM_017006779.1:c.3699A= XP_016862268.1:p.Pro1233=
XM_017006780.1:c.3699A= XP_016862269.1:p.Pro1233=
XM_017006783.1:c.3471A= XP_016862272.1:p.Pro1157=
XM_024453620.1:c.4110A= XP_024309388.1:p.Pro1370=
XM_024453621.1:c.3786A= XP_024309389.1:p.Pro1262=
XR_001740195.2:n.8358A=
NM_001080517.3:c.3975A= MANE Select NP_001073986.1:p.Pro1325=
NM_001292043.2:c.3681A= NP_001278972.1:p.Pro1227=
NM_001349451.2:c.3681A= NP_001336380.1:p.Pro1227=