Canonical Allele Identifier: CA351690692
Gene: SETD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475501C>A , CM000665.2:g.9475501C>A GRCh38
NC_000003.11:g.9517185C>A , CM000665.1:g.9517185C>A GRCh37
NC_000003.10:g.9492185C>A NCBI36
NG_034132.1:g.82802C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2694C>A
ENST00000682536.1:c.3835C>A ENSP00000507956.1:p.Pro1279Thr
ENST00000687014.1:n.4728C>A
ENST00000689167.1:n.2119C>A
ENST00000691925.1:n.6536C>A
ENST00000693430.1:n.5981C>A
ENST00000402198.7:c.3739C>A MANE Select ENSP00000385852.2:p.Pro1247Thr
ENST00000663774.1:c.*3885C>A ENSP00000499452.1:n.*3885C>A
ENST00000665872.1:c.*3808C>A ENSP00000499600.1:n.*3808C>A
ENST00000666307.1:c.*4113C>A ENSP00000499402.1:n.*4113C>A
ENST00000670063.1:c.*3844C>A ENSP00000499725.1:n.*3844C>A
ENST00000302463.10:c.3445C>A ENSP00000302028.6:p.Pro1149Thr
ENST00000399686.6:c.2722+345C>A
ENST00000402198.5:c.3739C>A ENSP00000385852.1:p.Pro1247Thr
ENST00000406341.5:c.3739C>A ENSP00000383939.1:p.Pro1247Thr
ENST00000407969.5:c.3796C>A ENSP00000384114.1:p.Pro1266Thr
ENST00000413704.5:c.2775C>A
ENST00000459941.1:n.870C>A
ENST00000466242.5:n.3080C>A
ENST00000466826.1:n.126C>A
ENST00000493918.5:n.3903C>A
NM_001080517.2:c.3739C>A NP_001073986.1:p.Pro1247Thr
NM_001292043.1:c.3445C>A NP_001278972.1:p.Pro1149Thr
XM_005265301.1:c.3796C>A XP_005265358.1:p.Pro1266Thr
XM_005265303.1:c.3739C>A XP_005265360.1:p.Pro1247Thr
XM_011533920.1:c.3913C>A XP_011532222.1:p.Pro1305Thr
XM_011533921.1:c.3913C>A XP_011532223.1:p.Pro1305Thr
XM_011533922.1:c.3892C>A XP_011532224.1:p.Pro1298Thr
XM_011533923.1:c.3892C>A XP_011532225.1:p.Pro1298Thr
XM_011533924.1:c.3892C>A XP_011532226.1:p.Pro1298Thr
XM_011533925.1:c.3874C>A XP_011532227.1:p.Pro1292Thr
XM_011533926.1:c.3856C>A XP_011532228.1:p.Pro1286Thr
XM_011533927.1:c.3856C>A XP_011532229.1:p.Pro1286Thr
XM_011533928.1:c.3835C>A XP_011532230.1:p.Pro1279Thr
XM_011533929.1:c.3817C>A XP_011532231.1:p.Pro1273Thr
XM_011533930.1:c.3778C>A XP_011532232.1:p.Pro1260Thr
XM_011533931.1:c.3502C>A XP_011532233.1:p.Pro1168Thr
XM_011533932.1:c.3463C>A XP_011532234.1:p.Pro1155Thr
XM_011533933.1:c.3463C>A XP_011532235.1:p.Pro1155Thr
NM_001349451.1:c.3445C>A NP_001336380.1:p.Pro1149Thr
XM_011533921.2:c.3913C>A XP_011532223.1:p.Pro1305Thr
XM_017006767.1:c.3913C>A XP_016862256.1:p.Pro1305Thr
XM_017006768.2:c.3892C>A XP_016862257.1:p.Pro1298Thr
XM_017006770.1:c.3856C>A XP_016862259.1:p.Pro1286Thr
XM_017006771.1:c.3853C>A XP_016862260.1:p.Pro1285Thr
XM_017006772.1:c.3817C>A XP_016862261.1:p.Pro1273Thr
XM_017006773.1:c.3817C>A XP_016862262.1:p.Pro1273Thr
XM_017006774.1:c.3796C>A XP_016862263.1:p.Pro1266Thr
XM_017006775.1:c.3760C>A XP_016862264.1:p.Pro1254Thr
XM_017006776.1:c.3502C>A XP_016862265.1:p.Pro1168Thr
XM_017006777.1:c.3502C>A XP_016862266.1:p.Pro1168Thr
XM_017006778.1:c.3502C>A XP_016862267.1:p.Pro1168Thr
XM_017006779.1:c.3463C>A XP_016862268.1:p.Pro1155Thr
XM_017006780.1:c.3463C>A XP_016862269.1:p.Pro1155Thr
XM_017006783.1:c.3235C>A XP_016862272.1:p.Pro1079Thr
XM_024453620.1:c.3874C>A XP_024309388.1:p.Pro1292Thr
XM_024453621.1:c.3550C>A XP_024309389.1:p.Pro1184Thr
XR_001740195.2:n.8122C>A
NM_001080517.3:c.3739C>A MANE Select NP_001073986.1:p.Pro1247Thr
NM_001292043.2:c.3445C>A NP_001278972.1:p.Pro1149Thr
NM_001349451.2:c.3445C>A NP_001336380.1:p.Pro1149Thr