Canonical Allele Identifier: CA432365863

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9515114C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9473430C>T , CM000665.2:g.9473430C>T	GRCh38
NC_000003.11:g.9515114C>T , CM000665.1:g.9515114C>T	GRCh37
NC_000003.10:g.9490114C>T	NCBI36
NG_034132.1:g.80731C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.1860C>T
ENST00000682536.1:c.3486C>T	ENSP00000507956.1:p.Phe1162=
ENST00000687014.1:n.3894C>T
ENST00000689167.1:n.959C>T
ENST00000691925.1:n.4465C>T
ENST00000693430.1:n.4821C>T
ENST00000402198.7:c.3390C>T MANE Select	ENSP00000385852.2:p.Phe1130=
ENST00000663774.1:c.*3536C>T	ENSP00000499452.1:n.*3536C>T
ENST00000665872.1:c.*3459C>T	ENSP00000499600.1:n.*3459C>T
ENST00000666307.1:c.*3764C>T	ENSP00000499402.1:n.*3764C>T
ENST00000670063.1:c.*3495C>T	ENSP00000499725.1:n.*3495C>T
ENST00000302463.10:c.3096C>T	ENSP00000302028.6:p.Phe1032=
ENST00000399686.6:c.2392C>T
ENST00000402198.5:c.3390C>T	ENSP00000385852.1:p.Phe1130=
ENST00000406341.5:c.3390C>T	ENSP00000383939.1:p.Phe1130=
ENST00000407969.5:c.3447C>T	ENSP00000384114.1:p.Phe1149=
ENST00000413704.5:c.2426C>T
ENST00000459941.1:n.36C>T
ENST00000466242.5:n.2731C>T
ENST00000479538.1:n.8C>T
ENST00000486465.5:n.458C>T
ENST00000492939.5:n.195C>T
ENST00000493918.5:n.3554C>T
NM_001080517.2:c.3390C>T	NP_001073986.1:p.Phe1130=
NM_001292043.1:c.3096C>T	NP_001278972.1:p.Phe1032=
XM_005265301.1:c.3447C>T	XP_005265358.1:p.Phe1149=
XM_005265303.1:c.3390C>T	XP_005265360.1:p.Phe1130=
XM_011533920.1:c.3564C>T	XP_011532222.1:p.Phe1188=
XM_011533921.1:c.3564C>T	XP_011532223.1:p.Phe1188=
XM_011533922.1:c.3543C>T	XP_011532224.1:p.Phe1181=
XM_011533923.1:c.3543C>T	XP_011532225.1:p.Phe1181=
XM_011533924.1:c.3543C>T	XP_011532226.1:p.Phe1181=
XM_011533925.1:c.3525C>T	XP_011532227.1:p.Phe1175=
XM_011533926.1:c.3507C>T	XP_011532228.1:p.Phe1169=
XM_011533927.1:c.3507C>T	XP_011532229.1:p.Phe1169=
XM_011533928.1:c.3486C>T	XP_011532230.1:p.Phe1162=
XM_011533929.1:c.3468C>T	XP_011532231.1:p.Phe1156=
XM_011533930.1:c.3429C>T	XP_011532232.1:p.Phe1143=
XM_011533931.1:c.3153C>T	XP_011532233.1:p.Phe1051=
XM_011533932.1:c.3114C>T	XP_011532234.1:p.Phe1038=
XM_011533933.1:c.3114C>T	XP_011532235.1:p.Phe1038=
XM_011533934.1:c.3564C>T	XP_011532236.1:p.Phe1188=
NM_001349451.1:c.3096C>T	NP_001336380.1:p.Phe1032=
XM_011533921.2:c.3564C>T	XP_011532223.1:p.Phe1188=
XM_017006767.1:c.3564C>T	XP_016862256.1:p.Phe1188=
XM_017006768.2:c.3543C>T	XP_016862257.1:p.Phe1181=
XM_017006770.1:c.3507C>T	XP_016862259.1:p.Phe1169=
XM_017006771.1:c.3504C>T	XP_016862260.1:p.Phe1168=
XM_017006772.1:c.3468C>T	XP_016862261.1:p.Phe1156=
XM_017006773.1:c.3468C>T	XP_016862262.1:p.Phe1156=
XM_017006774.1:c.3447C>T	XP_016862263.1:p.Phe1149=
XM_017006775.1:c.3411C>T	XP_016862264.1:p.Phe1137=
XM_017006776.1:c.3153C>T	XP_016862265.1:p.Phe1051=
XM_017006777.1:c.3153C>T	XP_016862266.1:p.Phe1051=
XM_017006778.1:c.3153C>T	XP_016862267.1:p.Phe1051=
XM_017006779.1:c.3114C>T	XP_016862268.1:p.Phe1038=
XM_017006780.1:c.3114C>T	XP_016862269.1:p.Phe1038=
XM_017006782.1:c.3564C>T	XP_016862271.1:p.Phe1188=
XM_017006783.1:c.2886C>T	XP_016862272.1:p.Phe962=
XM_024453620.1:c.3525C>T	XP_024309388.1:p.Phe1175=
XM_024453621.1:c.3201C>T	XP_024309389.1:p.Phe1067=
XR_001740195.2:n.7773C>T
NM_001080517.3:c.3390C>T MANE Select	NP_001073986.1:p.Phe1130=
NM_001292043.2:c.3096C>T	NP_001278972.1:p.Phe1032=
NM_001349451.2:c.3096C>T	NP_001336380.1:p.Phe1032=