Canonical Allele Identifier: CA1344742555
Gene: SETD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475638A= , CM000665.2:g.9475638A= GRCh38
NC_000003.11:g.9517322A= , CM000665.1:g.9517322A= GRCh37
NC_000003.10:g.9492322A= NCBI36
NG_034132.1:g.82939A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2831A=
ENST00000682536.1:c.3972A= ENSP00000507956.1:p.Ser1324=
ENST00000687014.1:n.4865A=
ENST00000689167.1:n.2256A=
ENST00000691925.1:n.6673A=
ENST00000693430.1:n.6118A=
ENST00000402198.7:c.3876A= MANE Select ENSP00000385852.2:p.Ser1292=
ENST00000663774.1:c.*4022A= ENSP00000499452.1:n.*4022A=
ENST00000665872.1:c.*3945A= ENSP00000499600.1:n.*3945A=
ENST00000666307.1:c.*4250A= ENSP00000499402.1:n.*4250A=
ENST00000670063.1:c.*3981A= ENSP00000499725.1:n.*3981A=
ENST00000302463.10:c.3582A= ENSP00000302028.6:p.Ser1194=
ENST00000399686.6:c.2722+482A=
ENST00000402198.5:c.3876A= ENSP00000385852.1:p.Ser1292=
ENST00000406341.5:c.3876A= ENSP00000383939.1:p.Ser1292=
ENST00000407969.5:c.3933A= ENSP00000384114.1:p.Ser1311=
ENST00000413704.5:c.2912A=
ENST00000459941.1:n.1007A=
ENST00000466242.5:n.3217A=
ENST00000466826.1:n.263A=
ENST00000493918.5:n.4040A=
NM_001080517.2:c.3876A= NP_001073986.1:p.Ser1292=
NM_001292043.1:c.3582A= NP_001278972.1:p.Ser1194=
XM_005265301.1:c.3933A= XP_005265358.1:p.Ser1311=
XM_005265303.1:c.3876A= XP_005265360.1:p.Ser1292=
XM_011533920.1:c.4050A= XP_011532222.1:p.Ser1350=
XM_011533921.1:c.4050A= XP_011532223.1:p.Ser1350=
XM_011533922.1:c.4029A= XP_011532224.1:p.Ser1343=
XM_011533923.1:c.4029A= XP_011532225.1:p.Ser1343=
XM_011533924.1:c.4029A= XP_011532226.1:p.Ser1343=
XM_011533925.1:c.4011A= XP_011532227.1:p.Ser1337=
XM_011533926.1:c.3993A= XP_011532228.1:p.Ser1331=
XM_011533927.1:c.3993A= XP_011532229.1:p.Ser1331=
XM_011533928.1:c.3972A= XP_011532230.1:p.Ser1324=
XM_011533929.1:c.3954A= XP_011532231.1:p.Ser1318=
XM_011533930.1:c.3915A= XP_011532232.1:p.Ser1305=
XM_011533931.1:c.3639A= XP_011532233.1:p.Ser1213=
XM_011533932.1:c.3600A= XP_011532234.1:p.Ser1200=
XM_011533933.1:c.3600A= XP_011532235.1:p.Ser1200=
NM_001349451.1:c.3582A= NP_001336380.1:p.Ser1194=
XM_011533921.2:c.4050A= XP_011532223.1:p.Ser1350=
XM_017006767.1:c.4050A= XP_016862256.1:p.Ser1350=
XM_017006768.2:c.4029A= XP_016862257.1:p.Ser1343=
XM_017006770.1:c.3993A= XP_016862259.1:p.Ser1331=
XM_017006771.1:c.3990A= XP_016862260.1:p.Ser1330=
XM_017006772.1:c.3954A= XP_016862261.1:p.Ser1318=
XM_017006773.1:c.3954A= XP_016862262.1:p.Ser1318=
XM_017006774.1:c.3933A= XP_016862263.1:p.Ser1311=
XM_017006775.1:c.3897A= XP_016862264.1:p.Ser1299=
XM_017006776.1:c.3639A= XP_016862265.1:p.Ser1213=
XM_017006777.1:c.3639A= XP_016862266.1:p.Ser1213=
XM_017006778.1:c.3639A= XP_016862267.1:p.Ser1213=
XM_017006779.1:c.3600A= XP_016862268.1:p.Ser1200=
XM_017006780.1:c.3600A= XP_016862269.1:p.Ser1200=
XM_017006783.1:c.3372A= XP_016862272.1:p.Ser1124=
XM_024453620.1:c.4011A= XP_024309388.1:p.Ser1337=
XM_024453621.1:c.3687A= XP_024309389.1:p.Ser1229=
XR_001740195.2:n.8259A=
NM_001080517.3:c.3876A= MANE Select NP_001073986.1:p.Ser1292=
NM_001292043.2:c.3582A= NP_001278972.1:p.Ser1194=
NM_001349451.2:c.3582A= NP_001336380.1:p.Ser1194=