Canonical Allele Identifier: CA2839040492
Gene: SETD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475237dup , CM000665.2:g.9475237dup GRCh38
NC_000003.11:g.9516921dup , CM000665.1:g.9516921dup GRCh37
NC_000003.10:g.9491921dup NCBI36
NG_034132.1:g.82538dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2675+81dup
ENST00000682536.1:c.3816+81dup ENSP00000507956.1:n.3816+81dup
ENST00000687014.1:n.4709+81dup
ENST00000689167.1:n.1855dup
ENST00000691925.1:n.6272dup
ENST00000693430.1:n.5717dup
ENST00000402198.7:c.3720+81dup MANE Select ENSP00000385852.2:n.3720+81dup
ENST00000663774.1:c.*3866+81dup ENSP00000499452.1:n.*3866+81dup
ENST00000665872.1:c.*3789+81dup ENSP00000499600.1:n.*3789+81dup
ENST00000666307.1:c.*4094+81dup ENSP00000499402.1:n.*4094+81dup
ENST00000670063.1:c.*3825+81dup ENSP00000499725.1:n.*3825+81dup
ENST00000302463.10:c.3426+81dup ENSP00000302028.6:n.3426+81dup
ENST00000399686.6:c.2722+81dup
ENST00000402198.5:c.3720+81dup ENSP00000385852.1:n.3720+81dup
ENST00000406341.5:c.3720+81dup ENSP00000383939.1:n.3720+81dup
ENST00000407969.5:c.3777+81dup ENSP00000384114.1:n.3777+81dup
ENST00000413704.5:c.2756+81dup
ENST00000459941.1:n.851+81dup
ENST00000466242.5:n.3061+81dup
ENST00000466826.1:n.107+81dup
ENST00000492939.5:n.606dup
ENST00000493918.5:n.3884+81dup
NM_001080517.2:c.3720+81dup NP_001073986.1:n.3720+81dup
NM_001292043.1:c.3426+81dup NP_001278972.1:n.3426+81dup
XM_005265301.1:c.3777+81dup XP_005265358.1:n.3777+81dup
XM_005265303.1:c.3720+81dup XP_005265360.1:n.3720+81dup
XM_011533920.1:c.3894+81dup XP_011532222.1:n.3894+81dup
XM_011533921.1:c.3894+81dup XP_011532223.1:n.3894+81dup
XM_011533922.1:c.3873+81dup XP_011532224.1:n.3873+81dup
XM_011533923.1:c.3873+81dup XP_011532225.1:n.3873+81dup
XM_011533924.1:c.3873+81dup XP_011532226.1:n.3873+81dup
XM_011533925.1:c.3855+81dup XP_011532227.1:n.3855+81dup
XM_011533926.1:c.3837+81dup XP_011532228.1:n.3837+81dup
XM_011533927.1:c.3837+81dup XP_011532229.1:n.3837+81dup
XM_011533928.1:c.3816+81dup XP_011532230.1:n.3816+81dup
XM_011533929.1:c.3798+81dup XP_011532231.1:n.3798+81dup
XM_011533930.1:c.3759+81dup XP_011532232.1:n.3759+81dup
XM_011533931.1:c.3483+81dup XP_011532233.1:n.3483+81dup
XM_011533932.1:c.3444+81dup XP_011532234.1:n.3444+81dup
XM_011533933.1:c.3444+81dup XP_011532235.1:n.3444+81dup
XM_011533934.1:c.3895-63dup XP_011532236.1:n.3895-63dup
NM_001349451.1:c.3426+81dup NP_001336380.1:n.3426+81dup
XM_011533921.2:c.3894+81dup XP_011532223.1:n.3894+81dup
XM_017006767.1:c.3894+81dup XP_016862256.1:n.3894+81dup
XM_017006768.2:c.3873+81dup XP_016862257.1:n.3873+81dup
XM_017006770.1:c.3837+81dup XP_016862259.1:n.3837+81dup
XM_017006771.1:c.3834+81dup XP_016862260.1:n.3834+81dup
XM_017006772.1:c.3798+81dup XP_016862261.1:n.3798+81dup
XM_017006773.1:c.3798+81dup XP_016862262.1:n.3798+81dup
XM_017006774.1:c.3777+81dup XP_016862263.1:n.3777+81dup
XM_017006775.1:c.3741+81dup XP_016862264.1:n.3741+81dup
XM_017006776.1:c.3483+81dup XP_016862265.1:n.3483+81dup
XM_017006777.1:c.3483+81dup XP_016862266.1:n.3483+81dup
XM_017006778.1:c.3483+81dup XP_016862267.1:n.3483+81dup
XM_017006779.1:c.3444+81dup XP_016862268.1:n.3444+81dup
XM_017006780.1:c.3444+81dup XP_016862269.1:n.3444+81dup
XM_017006782.1:c.3895-63dup XP_016862271.1:n.3895-63dup
XM_017006783.1:c.3216+81dup XP_016862272.1:n.3216+81dup
XM_024453620.1:c.3855+81dup XP_024309388.1:n.3855+81dup
XM_024453621.1:c.3531+81dup XP_024309389.1:n.3531+81dup
XR_001740195.2:n.8103+81dup
NM_001080517.3:c.3720+81dup MANE Select NP_001073986.1:n.3720+81dup
NM_001292043.2:c.3426+81dup NP_001278972.1:n.3426+81dup
NM_001349451.2:c.3426+81dup NP_001336380.1:n.3426+81dup