Canonical Allele Identifier: CA351692261

Gene: SETD5

Linked Data

• COSMIC: COSM1309515 ; COSM1309516
• MyVariant Identifiers: chr3:g.9517349C>A (hg19) ; chr3:g.9475665C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475665C>A , CM000665.2:g.9475665C>A	GRCh38
NC_000003.11:g.9517349C>A , CM000665.1:g.9517349C>A	GRCh37
NC_000003.10:g.9492349C>A	NCBI36
NG_034132.1:g.82966C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2858C>A
ENST00000682536.1:c.3999C>A	ENSP00000507956.1:p.Ser1333Arg
ENST00000687014.1:n.4892C>A
ENST00000689167.1:n.2283C>A
ENST00000691925.1:n.6700C>A
ENST00000693430.1:n.6145C>A
ENST00000402198.7:c.3903C>A MANE Select	ENSP00000385852.2:p.Ser1301Arg
ENST00000663774.1:c.*4049C>A	ENSP00000499452.1:n.*4049C>A
ENST00000665872.1:c.*3972C>A	ENSP00000499600.1:n.*3972C>A
ENST00000666307.1:c.*4277C>A	ENSP00000499402.1:n.*4277C>A
ENST00000670063.1:c.*4008C>A	ENSP00000499725.1:n.*4008C>A
ENST00000302463.10:c.3609C>A	ENSP00000302028.6:p.Ser1203Arg
ENST00000399686.6:c.2722+509C>A
ENST00000402198.5:c.3903C>A	ENSP00000385852.1:p.Ser1301Arg
ENST00000406341.5:c.3903C>A	ENSP00000383939.1:p.Ser1301Arg
ENST00000407969.5:c.3960C>A	ENSP00000384114.1:p.Ser1320Arg
ENST00000413704.5:c.2939C>A
ENST00000459941.1:n.1034C>A
ENST00000466242.5:n.3244C>A
ENST00000493918.5:n.4067C>A
NM_001080517.2:c.3903C>A	NP_001073986.1:p.Ser1301Arg
NM_001292043.1:c.3609C>A	NP_001278972.1:p.Ser1203Arg
XM_005265301.1:c.3960C>A	XP_005265358.1:p.Ser1320Arg
XM_005265303.1:c.3903C>A	XP_005265360.1:p.Ser1301Arg
XM_011533920.1:c.4077C>A	XP_011532222.1:p.Ser1359Arg
XM_011533921.1:c.4077C>A	XP_011532223.1:p.Ser1359Arg
XM_011533922.1:c.4056C>A	XP_011532224.1:p.Ser1352Arg
XM_011533923.1:c.4056C>A	XP_011532225.1:p.Ser1352Arg
XM_011533924.1:c.4056C>A	XP_011532226.1:p.Ser1352Arg
XM_011533925.1:c.4038C>A	XP_011532227.1:p.Ser1346Arg
XM_011533926.1:c.4020C>A	XP_011532228.1:p.Ser1340Arg
XM_011533927.1:c.4020C>A	XP_011532229.1:p.Ser1340Arg
XM_011533928.1:c.3999C>A	XP_011532230.1:p.Ser1333Arg
XM_011533929.1:c.3981C>A	XP_011532231.1:p.Ser1327Arg
XM_011533930.1:c.3942C>A	XP_011532232.1:p.Ser1314Arg
XM_011533931.1:c.3666C>A	XP_011532233.1:p.Ser1222Arg
XM_011533932.1:c.3627C>A	XP_011532234.1:p.Ser1209Arg
XM_011533933.1:c.3627C>A	XP_011532235.1:p.Ser1209Arg
NM_001349451.1:c.3609C>A	NP_001336380.1:p.Ser1203Arg
XM_011533921.2:c.4077C>A	XP_011532223.1:p.Ser1359Arg
XM_017006767.1:c.4077C>A	XP_016862256.1:p.Ser1359Arg
XM_017006768.2:c.4056C>A	XP_016862257.1:p.Ser1352Arg
XM_017006770.1:c.4020C>A	XP_016862259.1:p.Ser1340Arg
XM_017006771.1:c.4017C>A	XP_016862260.1:p.Ser1339Arg
XM_017006772.1:c.3981C>A	XP_016862261.1:p.Ser1327Arg
XM_017006773.1:c.3981C>A	XP_016862262.1:p.Ser1327Arg
XM_017006774.1:c.3960C>A	XP_016862263.1:p.Ser1320Arg
XM_017006775.1:c.3924C>A	XP_016862264.1:p.Ser1308Arg
XM_017006776.1:c.3666C>A	XP_016862265.1:p.Ser1222Arg
XM_017006777.1:c.3666C>A	XP_016862266.1:p.Ser1222Arg
XM_017006778.1:c.3666C>A	XP_016862267.1:p.Ser1222Arg
XM_017006779.1:c.3627C>A	XP_016862268.1:p.Ser1209Arg
XM_017006780.1:c.3627C>A	XP_016862269.1:p.Ser1209Arg
XM_017006783.1:c.3399C>A	XP_016862272.1:p.Ser1133Arg
XM_024453620.1:c.4038C>A	XP_024309388.1:p.Ser1346Arg
XM_024453621.1:c.3714C>A	XP_024309389.1:p.Ser1238Arg
XR_001740195.2:n.8286C>A
NM_001080517.3:c.3903C>A MANE Select	NP_001073986.1:p.Ser1301Arg
NM_001292043.2:c.3609C>A	NP_001278972.1:p.Ser1203Arg
NM_001349451.2:c.3609C>A	NP_001336380.1:p.Ser1203Arg