Canonical Allele Identifier: CA1344742412
Gene: SETD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475560T= , CM000665.2:g.9475560T= GRCh38
NC_000003.11:g.9517244T= , CM000665.1:g.9517244T= GRCh37
NC_000003.10:g.9492244T= NCBI36
NG_034132.1:g.82861T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2753T=
ENST00000682536.1:c.3894T= ENSP00000507956.1:p.Pro1298=
ENST00000687014.1:n.4787T=
ENST00000689167.1:n.2178T=
ENST00000691925.1:n.6595T=
ENST00000693430.1:n.6040T=
ENST00000402198.7:c.3798T= MANE Select ENSP00000385852.2:p.Pro1266=
ENST00000663774.1:c.*3944T= ENSP00000499452.1:n.*3944T=
ENST00000665872.1:c.*3867T= ENSP00000499600.1:n.*3867T=
ENST00000666307.1:c.*4172T= ENSP00000499402.1:n.*4172T=
ENST00000670063.1:c.*3903T= ENSP00000499725.1:n.*3903T=
ENST00000302463.10:c.3504T= ENSP00000302028.6:p.Pro1168=
ENST00000399686.6:c.2722+404T=
ENST00000402198.5:c.3798T= ENSP00000385852.1:p.Pro1266=
ENST00000406341.5:c.3798T= ENSP00000383939.1:p.Pro1266=
ENST00000407969.5:c.3855T= ENSP00000384114.1:p.Pro1285=
ENST00000413704.5:c.2834T=
ENST00000459941.1:n.929T=
ENST00000466242.5:n.3139T=
ENST00000466826.1:n.185T=
ENST00000493918.5:n.3962T=
NM_001080517.2:c.3798T= NP_001073986.1:p.Pro1266=
NM_001292043.1:c.3504T= NP_001278972.1:p.Pro1168=
XM_005265301.1:c.3855T= XP_005265358.1:p.Pro1285=
XM_005265303.1:c.3798T= XP_005265360.1:p.Pro1266=
XM_011533920.1:c.3972T= XP_011532222.1:p.Pro1324=
XM_011533921.1:c.3972T= XP_011532223.1:p.Pro1324=
XM_011533922.1:c.3951T= XP_011532224.1:p.Pro1317=
XM_011533923.1:c.3951T= XP_011532225.1:p.Pro1317=
XM_011533924.1:c.3951T= XP_011532226.1:p.Pro1317=
XM_011533925.1:c.3933T= XP_011532227.1:p.Pro1311=
XM_011533926.1:c.3915T= XP_011532228.1:p.Pro1305=
XM_011533927.1:c.3915T= XP_011532229.1:p.Pro1305=
XM_011533928.1:c.3894T= XP_011532230.1:p.Pro1298=
XM_011533929.1:c.3876T= XP_011532231.1:p.Pro1292=
XM_011533930.1:c.3837T= XP_011532232.1:p.Pro1279=
XM_011533931.1:c.3561T= XP_011532233.1:p.Pro1187=
XM_011533932.1:c.3522T= XP_011532234.1:p.Pro1174=
XM_011533933.1:c.3522T= XP_011532235.1:p.Pro1174=
NM_001349451.1:c.3504T= NP_001336380.1:p.Pro1168=
XM_011533921.2:c.3972T= XP_011532223.1:p.Pro1324=
XM_017006767.1:c.3972T= XP_016862256.1:p.Pro1324=
XM_017006768.2:c.3951T= XP_016862257.1:p.Pro1317=
XM_017006770.1:c.3915T= XP_016862259.1:p.Pro1305=
XM_017006771.1:c.3912T= XP_016862260.1:p.Pro1304=
XM_017006772.1:c.3876T= XP_016862261.1:p.Pro1292=
XM_017006773.1:c.3876T= XP_016862262.1:p.Pro1292=
XM_017006774.1:c.3855T= XP_016862263.1:p.Pro1285=
XM_017006775.1:c.3819T= XP_016862264.1:p.Pro1273=
XM_017006776.1:c.3561T= XP_016862265.1:p.Pro1187=
XM_017006777.1:c.3561T= XP_016862266.1:p.Pro1187=
XM_017006778.1:c.3561T= XP_016862267.1:p.Pro1187=
XM_017006779.1:c.3522T= XP_016862268.1:p.Pro1174=
XM_017006780.1:c.3522T= XP_016862269.1:p.Pro1174=
XM_017006783.1:c.3294T= XP_016862272.1:p.Pro1098=
XM_024453620.1:c.3933T= XP_024309388.1:p.Pro1311=
XM_024453621.1:c.3609T= XP_024309389.1:p.Pro1203=
XR_001740195.2:n.8181T=
NM_001080517.3:c.3798T= MANE Select NP_001073986.1:p.Pro1266=
NM_001292043.2:c.3504T= NP_001278972.1:p.Pro1168=
NM_001349451.2:c.3504T= NP_001336380.1:p.Pro1168=