Canonical Allele Identifier: CA351690999

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9517231T>G (hg19) ; chr3:g.9475547T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475547T>G , CM000665.2:g.9475547T>G	GRCh38
NC_000003.11:g.9517231T>G , CM000665.1:g.9517231T>G	GRCh37
NC_000003.10:g.9492231T>G	NCBI36
NG_034132.1:g.82848T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2740T>G
ENST00000682536.1:c.3881T>G	ENSP00000507956.1:p.Phe1294Cys
ENST00000687014.1:n.4774T>G
ENST00000689167.1:n.2165T>G
ENST00000691925.1:n.6582T>G
ENST00000693430.1:n.6027T>G
ENST00000402198.7:c.3785T>G MANE Select	ENSP00000385852.2:p.Phe1262Cys
ENST00000663774.1:c.*3931T>G	ENSP00000499452.1:n.*3931T>G
ENST00000665872.1:c.*3854T>G	ENSP00000499600.1:n.*3854T>G
ENST00000666307.1:c.*4159T>G	ENSP00000499402.1:n.*4159T>G
ENST00000670063.1:c.*3890T>G	ENSP00000499725.1:n.*3890T>G
ENST00000302463.10:c.3491T>G	ENSP00000302028.6:p.Phe1164Cys
ENST00000399686.6:c.2722+391T>G
ENST00000402198.5:c.3785T>G	ENSP00000385852.1:p.Phe1262Cys
ENST00000406341.5:c.3785T>G	ENSP00000383939.1:p.Phe1262Cys
ENST00000407969.5:c.3842T>G	ENSP00000384114.1:p.Phe1281Cys
ENST00000413704.5:c.2821T>G
ENST00000459941.1:n.916T>G
ENST00000466242.5:n.3126T>G
ENST00000466826.1:n.172T>G
ENST00000493918.5:n.3949T>G
NM_001080517.2:c.3785T>G	NP_001073986.1:p.Phe1262Cys
NM_001292043.1:c.3491T>G	NP_001278972.1:p.Phe1164Cys
XM_005265301.1:c.3842T>G	XP_005265358.1:p.Phe1281Cys
XM_005265303.1:c.3785T>G	XP_005265360.1:p.Phe1262Cys
XM_011533920.1:c.3959T>G	XP_011532222.1:p.Phe1320Cys
XM_011533921.1:c.3959T>G	XP_011532223.1:p.Phe1320Cys
XM_011533922.1:c.3938T>G	XP_011532224.1:p.Phe1313Cys
XM_011533923.1:c.3938T>G	XP_011532225.1:p.Phe1313Cys
XM_011533924.1:c.3938T>G	XP_011532226.1:p.Phe1313Cys
XM_011533925.1:c.3920T>G	XP_011532227.1:p.Phe1307Cys
XM_011533926.1:c.3902T>G	XP_011532228.1:p.Phe1301Cys
XM_011533927.1:c.3902T>G	XP_011532229.1:p.Phe1301Cys
XM_011533928.1:c.3881T>G	XP_011532230.1:p.Phe1294Cys
XM_011533929.1:c.3863T>G	XP_011532231.1:p.Phe1288Cys
XM_011533930.1:c.3824T>G	XP_011532232.1:p.Phe1275Cys
XM_011533931.1:c.3548T>G	XP_011532233.1:p.Phe1183Cys
XM_011533932.1:c.3509T>G	XP_011532234.1:p.Phe1170Cys
XM_011533933.1:c.3509T>G	XP_011532235.1:p.Phe1170Cys
NM_001349451.1:c.3491T>G	NP_001336380.1:p.Phe1164Cys
XM_011533921.2:c.3959T>G	XP_011532223.1:p.Phe1320Cys
XM_017006767.1:c.3959T>G	XP_016862256.1:p.Phe1320Cys
XM_017006768.2:c.3938T>G	XP_016862257.1:p.Phe1313Cys
XM_017006770.1:c.3902T>G	XP_016862259.1:p.Phe1301Cys
XM_017006771.1:c.3899T>G	XP_016862260.1:p.Phe1300Cys
XM_017006772.1:c.3863T>G	XP_016862261.1:p.Phe1288Cys
XM_017006773.1:c.3863T>G	XP_016862262.1:p.Phe1288Cys
XM_017006774.1:c.3842T>G	XP_016862263.1:p.Phe1281Cys
XM_017006775.1:c.3806T>G	XP_016862264.1:p.Phe1269Cys
XM_017006776.1:c.3548T>G	XP_016862265.1:p.Phe1183Cys
XM_017006777.1:c.3548T>G	XP_016862266.1:p.Phe1183Cys
XM_017006778.1:c.3548T>G	XP_016862267.1:p.Phe1183Cys
XM_017006779.1:c.3509T>G	XP_016862268.1:p.Phe1170Cys
XM_017006780.1:c.3509T>G	XP_016862269.1:p.Phe1170Cys
XM_017006783.1:c.3281T>G	XP_016862272.1:p.Phe1094Cys
XM_024453620.1:c.3920T>G	XP_024309388.1:p.Phe1307Cys
XM_024453621.1:c.3596T>G	XP_024309389.1:p.Phe1199Cys
XR_001740195.2:n.8168T>G
NM_001080517.3:c.3785T>G MANE Select	NP_001073986.1:p.Phe1262Cys
NM_001292043.2:c.3491T>G	NP_001278972.1:p.Phe1164Cys
NM_001349451.2:c.3491T>G	NP_001336380.1:p.Phe1164Cys