Canonical Allele Identifier: CA351684952

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9514964A>T (hg19) ; chr3:g.9473280A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9473280A>T , CM000665.2:g.9473280A>T	GRCh38
NC_000003.11:g.9514964A>T , CM000665.1:g.9514964A>T	GRCh37
NC_000003.10:g.9489964A>T	NCBI36
NG_034132.1:g.80581A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.1710A>T
ENST00000682536.1:c.3336A>T	ENSP00000507956.1:p.Glu1112Asp
ENST00000687014.1:n.3744A>T
ENST00000689167.1:n.809A>T
ENST00000691925.1:n.4315A>T
ENST00000693430.1:n.4671A>T
ENST00000402198.7:c.3240A>T MANE Select	ENSP00000385852.2:p.Glu1080Asp
ENST00000663774.1:c.*3386A>T	ENSP00000499452.1:n.*3386A>T
ENST00000665872.1:c.*3309A>T	ENSP00000499600.1:n.*3309A>T
ENST00000666307.1:c.*3614A>T	ENSP00000499402.1:n.*3614A>T
ENST00000670063.1:c.*3345A>T	ENSP00000499725.1:n.*3345A>T
ENST00000302463.10:c.2946A>T	ENSP00000302028.6:p.Glu982Asp
ENST00000399686.6:c.2242A>T
ENST00000402198.5:c.3240A>T	ENSP00000385852.1:p.Glu1080Asp
ENST00000406341.5:c.3240A>T	ENSP00000383939.1:p.Glu1080Asp
ENST00000407969.5:c.3297A>T	ENSP00000384114.1:p.Glu1099Asp
ENST00000413704.5:c.2276A>T
ENST00000421188.1:c.1231A>T
ENST00000466242.5:n.2581A>T
ENST00000486465.5:n.308A>T
ENST00000492939.5:n.45A>T
ENST00000493918.5:n.3404A>T
NM_001080517.2:c.3240A>T	NP_001073986.1:p.Glu1080Asp
NM_001292043.1:c.2946A>T	NP_001278972.1:p.Glu982Asp
XM_005265301.1:c.3297A>T	XP_005265358.1:p.Glu1099Asp
XM_005265303.1:c.3240A>T	XP_005265360.1:p.Glu1080Asp
XM_011533920.1:c.3414A>T	XP_011532222.1:p.Glu1138Asp
XM_011533921.1:c.3414A>T	XP_011532223.1:p.Glu1138Asp
XM_011533922.1:c.3393A>T	XP_011532224.1:p.Glu1131Asp
XM_011533923.1:c.3393A>T	XP_011532225.1:p.Glu1131Asp
XM_011533924.1:c.3393A>T	XP_011532226.1:p.Glu1131Asp
XM_011533925.1:c.3375A>T	XP_011532227.1:p.Glu1125Asp
XM_011533926.1:c.3357A>T	XP_011532228.1:p.Glu1119Asp
XM_011533927.1:c.3357A>T	XP_011532229.1:p.Glu1119Asp
XM_011533928.1:c.3336A>T	XP_011532230.1:p.Glu1112Asp
XM_011533929.1:c.3318A>T	XP_011532231.1:p.Glu1106Asp
XM_011533930.1:c.3279A>T	XP_011532232.1:p.Glu1093Asp
XM_011533931.1:c.3003A>T	XP_011532233.1:p.Glu1001Asp
XM_011533932.1:c.2964A>T	XP_011532234.1:p.Glu988Asp
XM_011533933.1:c.2964A>T	XP_011532235.1:p.Glu988Asp
XM_011533934.1:c.3414A>T	XP_011532236.1:p.Glu1138Asp
NM_001349451.1:c.2946A>T	NP_001336380.1:p.Glu982Asp
XM_011533921.2:c.3414A>T	XP_011532223.1:p.Glu1138Asp
XM_017006767.1:c.3414A>T	XP_016862256.1:p.Glu1138Asp
XM_017006768.2:c.3393A>T	XP_016862257.1:p.Glu1131Asp
XM_017006770.1:c.3357A>T	XP_016862259.1:p.Glu1119Asp
XM_017006771.1:c.3354A>T	XP_016862260.1:p.Glu1118Asp
XM_017006772.1:c.3318A>T	XP_016862261.1:p.Glu1106Asp
XM_017006773.1:c.3318A>T	XP_016862262.1:p.Glu1106Asp
XM_017006774.1:c.3297A>T	XP_016862263.1:p.Glu1099Asp
XM_017006775.1:c.3261A>T	XP_016862264.1:p.Glu1087Asp
XM_017006776.1:c.3003A>T	XP_016862265.1:p.Glu1001Asp
XM_017006777.1:c.3003A>T	XP_016862266.1:p.Glu1001Asp
XM_017006778.1:c.3003A>T	XP_016862267.1:p.Glu1001Asp
XM_017006779.1:c.2964A>T	XP_016862268.1:p.Glu988Asp
XM_017006780.1:c.2964A>T	XP_016862269.1:p.Glu988Asp
XM_017006782.1:c.3414A>T	XP_016862271.1:p.Glu1138Asp
XM_017006783.1:c.2736A>T	XP_016862272.1:p.Glu912Asp
XM_024453620.1:c.3375A>T	XP_024309388.1:p.Glu1125Asp
XM_024453621.1:c.3051A>T	XP_024309389.1:p.Glu1017Asp
XR_001740195.2:n.7623A>T
NM_001080517.3:c.3240A>T MANE Select	NP_001073986.1:p.Glu1080Asp
NM_001292043.2:c.2946A>T	NP_001278972.1:p.Glu982Asp
NM_001349451.2:c.2946A>T	NP_001336380.1:p.Glu982Asp