Canonical Allele Identifier: CA432528368

Gene: SETD5

Linked Data

• gnomAD v4: 3-9475518-A-G
• MyVariant Identifiers: chr3:g.9517202A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475518A>G , CM000665.2:g.9475518A>G	GRCh38
NC_000003.11:g.9517202A>G , CM000665.1:g.9517202A>G	GRCh37
NC_000003.10:g.9492202A>G	NCBI36
NG_034132.1:g.82819A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682236.1:n.2711A>G
ENST00000682536.1:c.3852A>G	ENSP00000507956.1:p.Gln1284=
ENST00000687014.1:n.4745A>G
ENST00000689167.1:n.2136A>G
ENST00000691925.1:n.6553A>G
ENST00000693430.1:n.5998A>G
ENST00000402198.7:c.3756A>G MANE Select	ENSP00000385852.2:p.Gln1252=
ENST00000663774.1:c.*3902A>G	ENSP00000499452.1:n.*3902A>G
ENST00000665872.1:c.*3825A>G	ENSP00000499600.1:n.*3825A>G
ENST00000666307.1:c.*4130A>G	ENSP00000499402.1:n.*4130A>G
ENST00000670063.1:c.*3861A>G	ENSP00000499725.1:n.*3861A>G
ENST00000302463.10:c.3462A>G	ENSP00000302028.6:p.Gln1154=
ENST00000399686.6:c.2722+362A>G
ENST00000402198.5:c.3756A>G	ENSP00000385852.1:p.Gln1252=
ENST00000406341.5:c.3756A>G	ENSP00000383939.1:p.Gln1252=
ENST00000407969.5:c.3813A>G	ENSP00000384114.1:p.Gln1271=
ENST00000413704.5:c.2792A>G
ENST00000459941.1:n.887A>G
ENST00000466242.5:n.3097A>G
ENST00000466826.1:n.143A>G
ENST00000493918.5:n.3920A>G
NM_001080517.2:c.3756A>G	NP_001073986.1:p.Gln1252=
NM_001292043.1:c.3462A>G	NP_001278972.1:p.Gln1154=
XM_005265301.1:c.3813A>G	XP_005265358.1:p.Gln1271=
XM_005265303.1:c.3756A>G	XP_005265360.1:p.Gln1252=
XM_011533920.1:c.3930A>G	XP_011532222.1:p.Gln1310=
XM_011533921.1:c.3930A>G	XP_011532223.1:p.Gln1310=
XM_011533922.1:c.3909A>G	XP_011532224.1:p.Gln1303=
XM_011533923.1:c.3909A>G	XP_011532225.1:p.Gln1303=
XM_011533924.1:c.3909A>G	XP_011532226.1:p.Gln1303=
XM_011533925.1:c.3891A>G	XP_011532227.1:p.Gln1297=
XM_011533926.1:c.3873A>G	XP_011532228.1:p.Gln1291=
XM_011533927.1:c.3873A>G	XP_011532229.1:p.Gln1291=
XM_011533928.1:c.3852A>G	XP_011532230.1:p.Gln1284=
XM_011533929.1:c.3834A>G	XP_011532231.1:p.Gln1278=
XM_011533930.1:c.3795A>G	XP_011532232.1:p.Gln1265=
XM_011533931.1:c.3519A>G	XP_011532233.1:p.Gln1173=
XM_011533932.1:c.3480A>G	XP_011532234.1:p.Gln1160=
XM_011533933.1:c.3480A>G	XP_011532235.1:p.Gln1160=
NM_001349451.1:c.3462A>G	NP_001336380.1:p.Gln1154=
XM_011533921.2:c.3930A>G	XP_011532223.1:p.Gln1310=
XM_017006767.1:c.3930A>G	XP_016862256.1:p.Gln1310=
XM_017006768.2:c.3909A>G	XP_016862257.1:p.Gln1303=
XM_017006770.1:c.3873A>G	XP_016862259.1:p.Gln1291=
XM_017006771.1:c.3870A>G	XP_016862260.1:p.Gln1290=
XM_017006772.1:c.3834A>G	XP_016862261.1:p.Gln1278=
XM_017006773.1:c.3834A>G	XP_016862262.1:p.Gln1278=
XM_017006774.1:c.3813A>G	XP_016862263.1:p.Gln1271=
XM_017006775.1:c.3777A>G	XP_016862264.1:p.Gln1259=
XM_017006776.1:c.3519A>G	XP_016862265.1:p.Gln1173=
XM_017006777.1:c.3519A>G	XP_016862266.1:p.Gln1173=
XM_017006778.1:c.3519A>G	XP_016862267.1:p.Gln1173=
XM_017006779.1:c.3480A>G	XP_016862268.1:p.Gln1160=
XM_017006780.1:c.3480A>G	XP_016862269.1:p.Gln1160=
XM_017006783.1:c.3252A>G	XP_016862272.1:p.Gln1084=
XM_024453620.1:c.3891A>G	XP_024309388.1:p.Gln1297=
XM_024453621.1:c.3567A>G	XP_024309389.1:p.Gln1189=
XR_001740195.2:n.8139A>G
NM_001080517.3:c.3756A>G MANE Select	NP_001073986.1:p.Gln1252=
NM_001292043.2:c.3462A>G	NP_001278972.1:p.Gln1154=
NM_001349451.2:c.3462A>G	NP_001336380.1:p.Gln1154=