Canonical Allele Identifier: CA432365687

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9514925C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9473241C>T , CM000665.2:g.9473241C>T	GRCh38
NC_000003.11:g.9514925C>T , CM000665.1:g.9514925C>T	GRCh37
NC_000003.10:g.9489925C>T	NCBI36
NG_034132.1:g.80542C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.1671C>T
ENST00000682536.1:c.3297C>T	ENSP00000507956.1:p.Ser1099=
ENST00000687014.1:n.3705C>T
ENST00000689167.1:n.770C>T
ENST00000691925.1:n.4276C>T
ENST00000693430.1:n.4632C>T
ENST00000402198.7:c.3201C>T MANE Select	ENSP00000385852.2:p.Ser1067=
ENST00000663774.1:c.*3347C>T	ENSP00000499452.1:n.*3347C>T
ENST00000665872.1:c.*3270C>T	ENSP00000499600.1:n.*3270C>T
ENST00000666307.1:c.*3575C>T	ENSP00000499402.1:n.*3575C>T
ENST00000670063.1:c.*3306C>T	ENSP00000499725.1:n.*3306C>T
ENST00000302463.10:c.2907C>T	ENSP00000302028.6:p.Ser969=
ENST00000399686.6:c.2203C>T
ENST00000402198.5:c.3201C>T	ENSP00000385852.1:p.Ser1067=
ENST00000406341.5:c.3201C>T	ENSP00000383939.1:p.Ser1067=
ENST00000407969.5:c.3258C>T	ENSP00000384114.1:p.Ser1086=
ENST00000413704.5:c.2237C>T
ENST00000421188.1:c.1192C>T
ENST00000466242.5:n.2542C>T
ENST00000486465.5:n.269C>T
ENST00000492939.5:n.6C>T
ENST00000493918.5:n.3365C>T
NM_001080517.2:c.3201C>T	NP_001073986.1:p.Ser1067=
NM_001292043.1:c.2907C>T	NP_001278972.1:p.Ser969=
XM_005265301.1:c.3258C>T	XP_005265358.1:p.Ser1086=
XM_005265303.1:c.3201C>T	XP_005265360.1:p.Ser1067=
XM_011533920.1:c.3375C>T	XP_011532222.1:p.Ser1125=
XM_011533921.1:c.3375C>T	XP_011532223.1:p.Ser1125=
XM_011533922.1:c.3354C>T	XP_011532224.1:p.Ser1118=
XM_011533923.1:c.3354C>T	XP_011532225.1:p.Ser1118=
XM_011533924.1:c.3354C>T	XP_011532226.1:p.Ser1118=
XM_011533925.1:c.3336C>T	XP_011532227.1:p.Ser1112=
XM_011533926.1:c.3318C>T	XP_011532228.1:p.Ser1106=
XM_011533927.1:c.3318C>T	XP_011532229.1:p.Ser1106=
XM_011533928.1:c.3297C>T	XP_011532230.1:p.Ser1099=
XM_011533929.1:c.3279C>T	XP_011532231.1:p.Ser1093=
XM_011533930.1:c.3240C>T	XP_011532232.1:p.Ser1080=
XM_011533931.1:c.2964C>T	XP_011532233.1:p.Ser988=
XM_011533932.1:c.2925C>T	XP_011532234.1:p.Ser975=
XM_011533933.1:c.2925C>T	XP_011532235.1:p.Ser975=
XM_011533934.1:c.3375C>T	XP_011532236.1:p.Ser1125=
NM_001349451.1:c.2907C>T	NP_001336380.1:p.Ser969=
XM_011533921.2:c.3375C>T	XP_011532223.1:p.Ser1125=
XM_017006767.1:c.3375C>T	XP_016862256.1:p.Ser1125=
XM_017006768.2:c.3354C>T	XP_016862257.1:p.Ser1118=
XM_017006770.1:c.3318C>T	XP_016862259.1:p.Ser1106=
XM_017006771.1:c.3315C>T	XP_016862260.1:p.Ser1105=
XM_017006772.1:c.3279C>T	XP_016862261.1:p.Ser1093=
XM_017006773.1:c.3279C>T	XP_016862262.1:p.Ser1093=
XM_017006774.1:c.3258C>T	XP_016862263.1:p.Ser1086=
XM_017006775.1:c.3222C>T	XP_016862264.1:p.Ser1074=
XM_017006776.1:c.2964C>T	XP_016862265.1:p.Ser988=
XM_017006777.1:c.2964C>T	XP_016862266.1:p.Ser988=
XM_017006778.1:c.2964C>T	XP_016862267.1:p.Ser988=
XM_017006779.1:c.2925C>T	XP_016862268.1:p.Ser975=
XM_017006780.1:c.2925C>T	XP_016862269.1:p.Ser975=
XM_017006782.1:c.3375C>T	XP_016862271.1:p.Ser1125=
XM_017006783.1:c.2697C>T	XP_016862272.1:p.Ser899=
XM_024453620.1:c.3336C>T	XP_024309388.1:p.Ser1112=
XM_024453621.1:c.3012C>T	XP_024309389.1:p.Ser1004=
XR_001740195.2:n.7584C>T
NM_001080517.3:c.3201C>T MANE Select	NP_001073986.1:p.Ser1067=
NM_001292043.2:c.2907C>T	NP_001278972.1:p.Ser969=
NM_001349451.2:c.2907C>T	NP_001336380.1:p.Ser969=