Canonical Allele Identifier: CA1344742641

Gene: SETD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475681T= , CM000665.2:g.9475681T=	GRCh38
NC_000003.11:g.9517365T= , CM000665.1:g.9517365T=	GRCh37
NC_000003.10:g.9492365T=	NCBI36
NG_034132.1:g.82982T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2874T=
ENST00000682536.1:c.4015T=	ENSP00000507956.1:p.Ser1339=
ENST00000687014.1:n.4908T=
ENST00000689167.1:n.2299T=
ENST00000693430.1:n.6161T=
ENST00000402198.7:c.3919T= MANE Select	ENSP00000385852.2:p.Ser1307=
ENST00000663774.1:c.*4065T=	ENSP00000499452.1:n.*4065T=
ENST00000665872.1:c.*3988T=	ENSP00000499600.1:n.*3988T=
ENST00000666307.1:c.*4293T=	ENSP00000499402.1:n.*4293T=
ENST00000670063.1:c.*4024T=	ENSP00000499725.1:n.*4024T=
ENST00000302463.10:c.3625T=	ENSP00000302028.6:p.Ser1209=
ENST00000399686.6:c.2722+525T=
ENST00000402198.5:c.3919T=	ENSP00000385852.1:p.Ser1307=
ENST00000406341.5:c.3919T=	ENSP00000383939.1:p.Ser1307=
ENST00000407969.5:c.3976T=	ENSP00000384114.1:p.Ser1326=
ENST00000413704.5:c.2955T=
ENST00000459941.1:n.1050T=
ENST00000466242.5:n.3260T=
ENST00000493918.5:n.4083T=
NM_001080517.2:c.3919T=	NP_001073986.1:p.Ser1307=
NM_001292043.1:c.3625T=	NP_001278972.1:p.Ser1209=
XM_005265301.1:c.3976T=	XP_005265358.1:p.Ser1326=
XM_005265303.1:c.3919T=	XP_005265360.1:p.Ser1307=
XM_011533920.1:c.4093T=	XP_011532222.1:p.Ser1365=
XM_011533921.1:c.4093T=	XP_011532223.1:p.Ser1365=
XM_011533922.1:c.4072T=	XP_011532224.1:p.Ser1358=
XM_011533923.1:c.4072T=	XP_011532225.1:p.Ser1358=
XM_011533924.1:c.4072T=	XP_011532226.1:p.Ser1358=
XM_011533925.1:c.4054T=	XP_011532227.1:p.Ser1352=
XM_011533926.1:c.4036T=	XP_011532228.1:p.Ser1346=
XM_011533927.1:c.4036T=	XP_011532229.1:p.Ser1346=
XM_011533928.1:c.4015T=	XP_011532230.1:p.Ser1339=
XM_011533929.1:c.3997T=	XP_011532231.1:p.Ser1333=
XM_011533930.1:c.3958T=	XP_011532232.1:p.Ser1320=
XM_011533931.1:c.3682T=	XP_011532233.1:p.Ser1228=
XM_011533932.1:c.3643T=	XP_011532234.1:p.Ser1215=
XM_011533933.1:c.3643T=	XP_011532235.1:p.Ser1215=
NM_001349451.1:c.3625T=	NP_001336380.1:p.Ser1209=
XM_011533921.2:c.4093T=	XP_011532223.1:p.Ser1365=
XM_017006767.1:c.4093T=	XP_016862256.1:p.Ser1365=
XM_017006768.2:c.4072T=	XP_016862257.1:p.Ser1358=
XM_017006770.1:c.4036T=	XP_016862259.1:p.Ser1346=
XM_017006771.1:c.4033T=	XP_016862260.1:p.Ser1345=
XM_017006772.1:c.3997T=	XP_016862261.1:p.Ser1333=
XM_017006773.1:c.3997T=	XP_016862262.1:p.Ser1333=
XM_017006774.1:c.3976T=	XP_016862263.1:p.Ser1326=
XM_017006775.1:c.3940T=	XP_016862264.1:p.Ser1314=
XM_017006776.1:c.3682T=	XP_016862265.1:p.Ser1228=
XM_017006777.1:c.3682T=	XP_016862266.1:p.Ser1228=
XM_017006778.1:c.3682T=	XP_016862267.1:p.Ser1228=
XM_017006779.1:c.3643T=	XP_016862268.1:p.Ser1215=
XM_017006780.1:c.3643T=	XP_016862269.1:p.Ser1215=
XM_017006783.1:c.3415T=	XP_016862272.1:p.Ser1139=
XM_024453620.1:c.4054T=	XP_024309388.1:p.Ser1352=
XM_024453621.1:c.3730T=	XP_024309389.1:p.Ser1244=
XR_001740195.2:n.8302T=
NM_001080517.3:c.3919T= MANE Select	NP_001073986.1:p.Ser1307=
NM_001292043.2:c.3625T=	NP_001278972.1:p.Ser1209=
NM_001349451.2:c.3625T=	NP_001336380.1:p.Ser1209=