Canonical Allele Identifier: CA1344742658

Gene: SETD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475689C= , CM000665.2:g.9475689C=	GRCh38
NC_000003.11:g.9517373C= , CM000665.1:g.9517373C=	GRCh37
NC_000003.10:g.9492373C=	NCBI36
NG_034132.1:g.82990C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2882C=
ENST00000682536.1:c.4023C=	ENSP00000507956.1:p.Asp1341=
ENST00000687014.1:n.4916C=
ENST00000689167.1:n.2307C=
ENST00000693430.1:n.6169C=
ENST00000402198.7:c.3927C= MANE Select	ENSP00000385852.2:p.Asp1309=
ENST00000663774.1:c.*4073C=	ENSP00000499452.1:n.*4073C=
ENST00000665872.1:c.*3996C=	ENSP00000499600.1:n.*3996C=
ENST00000666307.1:c.*4301C=	ENSP00000499402.1:n.*4301C=
ENST00000670063.1:c.*4032C=	ENSP00000499725.1:n.*4032C=
ENST00000302463.10:c.3633C=	ENSP00000302028.6:p.Asp1211=
ENST00000399686.6:c.2722+533C=
ENST00000402198.5:c.3927C=	ENSP00000385852.1:p.Asp1309=
ENST00000406341.5:c.3927C=	ENSP00000383939.1:p.Asp1309=
ENST00000407969.5:c.3984C=	ENSP00000384114.1:p.Asp1328=
ENST00000413704.5:c.2963C=
ENST00000459941.1:n.1058C=
ENST00000466242.5:n.3268C=
ENST00000493918.5:n.4091C=
NM_001080517.2:c.3927C=	NP_001073986.1:p.Asp1309=
NM_001292043.1:c.3633C=	NP_001278972.1:p.Asp1211=
XM_005265301.1:c.3984C=	XP_005265358.1:p.Asp1328=
XM_005265303.1:c.3927C=	XP_005265360.1:p.Asp1309=
XM_011533920.1:c.4101C=	XP_011532222.1:p.Asp1367=
XM_011533921.1:c.4101C=	XP_011532223.1:p.Asp1367=
XM_011533922.1:c.4080C=	XP_011532224.1:p.Asp1360=
XM_011533923.1:c.4080C=	XP_011532225.1:p.Asp1360=
XM_011533924.1:c.4080C=	XP_011532226.1:p.Asp1360=
XM_011533925.1:c.4062C=	XP_011532227.1:p.Asp1354=
XM_011533926.1:c.4044C=	XP_011532228.1:p.Asp1348=
XM_011533927.1:c.4044C=	XP_011532229.1:p.Asp1348=
XM_011533928.1:c.4023C=	XP_011532230.1:p.Asp1341=
XM_011533929.1:c.4005C=	XP_011532231.1:p.Asp1335=
XM_011533930.1:c.3966C=	XP_011532232.1:p.Asp1322=
XM_011533931.1:c.3690C=	XP_011532233.1:p.Asp1230=
XM_011533932.1:c.3651C=	XP_011532234.1:p.Asp1217=
XM_011533933.1:c.3651C=	XP_011532235.1:p.Asp1217=
NM_001349451.1:c.3633C=	NP_001336380.1:p.Asp1211=
XM_011533921.2:c.4101C=	XP_011532223.1:p.Asp1367=
XM_017006767.1:c.4101C=	XP_016862256.1:p.Asp1367=
XM_017006768.2:c.4080C=	XP_016862257.1:p.Asp1360=
XM_017006770.1:c.4044C=	XP_016862259.1:p.Asp1348=
XM_017006771.1:c.4041C=	XP_016862260.1:p.Asp1347=
XM_017006772.1:c.4005C=	XP_016862261.1:p.Asp1335=
XM_017006773.1:c.4005C=	XP_016862262.1:p.Asp1335=
XM_017006774.1:c.3984C=	XP_016862263.1:p.Asp1328=
XM_017006775.1:c.3948C=	XP_016862264.1:p.Asp1316=
XM_017006776.1:c.3690C=	XP_016862265.1:p.Asp1230=
XM_017006777.1:c.3690C=	XP_016862266.1:p.Asp1230=
XM_017006778.1:c.3690C=	XP_016862267.1:p.Asp1230=
XM_017006779.1:c.3651C=	XP_016862268.1:p.Asp1217=
XM_017006780.1:c.3651C=	XP_016862269.1:p.Asp1217=
XM_017006783.1:c.3423C=	XP_016862272.1:p.Asp1141=
XM_024453620.1:c.4062C=	XP_024309388.1:p.Asp1354=
XM_024453621.1:c.3738C=	XP_024309389.1:p.Asp1246=
XR_001740195.2:n.8310C=
NM_001080517.3:c.3927C= MANE Select	NP_001073986.1:p.Asp1309=
NM_001292043.2:c.3633C=	NP_001278972.1:p.Asp1211=
NM_001349451.2:c.3633C=	NP_001336380.1:p.Asp1211=