Canonical Allele Identifier: CA1344742588
Gene: SETD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475658A= , CM000665.2:g.9475658A= GRCh38
NC_000003.11:g.9517342A= , CM000665.1:g.9517342A= GRCh37
NC_000003.10:g.9492342A= NCBI36
NG_034132.1:g.82959A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2851A=
ENST00000682536.1:c.3992A= ENSP00000507956.1:p.Tyr1331=
ENST00000687014.1:n.4885A=
ENST00000689167.1:n.2276A=
ENST00000691925.1:n.6693A=
ENST00000693430.1:n.6138A=
ENST00000402198.7:c.3896A= MANE Select ENSP00000385852.2:p.Tyr1299=
ENST00000663774.1:c.*4042A= ENSP00000499452.1:n.*4042A=
ENST00000665872.1:c.*3965A= ENSP00000499600.1:n.*3965A=
ENST00000666307.1:c.*4270A= ENSP00000499402.1:n.*4270A=
ENST00000670063.1:c.*4001A= ENSP00000499725.1:n.*4001A=
ENST00000302463.10:c.3602A= ENSP00000302028.6:p.Tyr1201=
ENST00000399686.6:c.2722+502A=
ENST00000402198.5:c.3896A= ENSP00000385852.1:p.Tyr1299=
ENST00000406341.5:c.3896A= ENSP00000383939.1:p.Tyr1299=
ENST00000407969.5:c.3953A= ENSP00000384114.1:p.Tyr1318=
ENST00000413704.5:c.2932A=
ENST00000459941.1:n.1027A=
ENST00000466242.5:n.3237A=
ENST00000466826.1:n.283A=
ENST00000493918.5:n.4060A=
NM_001080517.2:c.3896A= NP_001073986.1:p.Tyr1299=
NM_001292043.1:c.3602A= NP_001278972.1:p.Tyr1201=
XM_005265301.1:c.3953A= XP_005265358.1:p.Tyr1318=
XM_005265303.1:c.3896A= XP_005265360.1:p.Tyr1299=
XM_011533920.1:c.4070A= XP_011532222.1:p.Tyr1357=
XM_011533921.1:c.4070A= XP_011532223.1:p.Tyr1357=
XM_011533922.1:c.4049A= XP_011532224.1:p.Tyr1350=
XM_011533923.1:c.4049A= XP_011532225.1:p.Tyr1350=
XM_011533924.1:c.4049A= XP_011532226.1:p.Tyr1350=
XM_011533925.1:c.4031A= XP_011532227.1:p.Tyr1344=
XM_011533926.1:c.4013A= XP_011532228.1:p.Tyr1338=
XM_011533927.1:c.4013A= XP_011532229.1:p.Tyr1338=
XM_011533928.1:c.3992A= XP_011532230.1:p.Tyr1331=
XM_011533929.1:c.3974A= XP_011532231.1:p.Tyr1325=
XM_011533930.1:c.3935A= XP_011532232.1:p.Tyr1312=
XM_011533931.1:c.3659A= XP_011532233.1:p.Tyr1220=
XM_011533932.1:c.3620A= XP_011532234.1:p.Tyr1207=
XM_011533933.1:c.3620A= XP_011532235.1:p.Tyr1207=
NM_001349451.1:c.3602A= NP_001336380.1:p.Tyr1201=
XM_011533921.2:c.4070A= XP_011532223.1:p.Tyr1357=
XM_017006767.1:c.4070A= XP_016862256.1:p.Tyr1357=
XM_017006768.2:c.4049A= XP_016862257.1:p.Tyr1350=
XM_017006770.1:c.4013A= XP_016862259.1:p.Tyr1338=
XM_017006771.1:c.4010A= XP_016862260.1:p.Tyr1337=
XM_017006772.1:c.3974A= XP_016862261.1:p.Tyr1325=
XM_017006773.1:c.3974A= XP_016862262.1:p.Tyr1325=
XM_017006774.1:c.3953A= XP_016862263.1:p.Tyr1318=
XM_017006775.1:c.3917A= XP_016862264.1:p.Tyr1306=
XM_017006776.1:c.3659A= XP_016862265.1:p.Tyr1220=
XM_017006777.1:c.3659A= XP_016862266.1:p.Tyr1220=
XM_017006778.1:c.3659A= XP_016862267.1:p.Tyr1220=
XM_017006779.1:c.3620A= XP_016862268.1:p.Tyr1207=
XM_017006780.1:c.3620A= XP_016862269.1:p.Tyr1207=
XM_017006783.1:c.3392A= XP_016862272.1:p.Tyr1131=
XM_024453620.1:c.4031A= XP_024309388.1:p.Tyr1344=
XM_024453621.1:c.3707A= XP_024309389.1:p.Tyr1236=
XR_001740195.2:n.8279A=
NM_001080517.3:c.3896A= MANE Select NP_001073986.1:p.Tyr1299=
NM_001292043.2:c.3602A= NP_001278972.1:p.Tyr1201=
NM_001349451.2:c.3602A= NP_001336380.1:p.Tyr1201=