Canonical Allele Identifier: CA432528751

Gene: SETD5

Linked Data

• gnomAD v4: 3-9475641-C-T
• MyVariant Identifiers: chr3:g.9517325C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475641C>T , CM000665.2:g.9475641C>T	GRCh38
NC_000003.11:g.9517325C>T , CM000665.1:g.9517325C>T	GRCh37
NC_000003.10:g.9492325C>T	NCBI36
NG_034132.1:g.82942C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2834C>T
ENST00000682536.1:c.3975C>T	ENSP00000507956.1:p.Ser1325=
ENST00000687014.1:n.4868C>T
ENST00000689167.1:n.2259C>T
ENST00000691925.1:n.6676C>T
ENST00000693430.1:n.6121C>T
ENST00000402198.7:c.3879C>T MANE Select	ENSP00000385852.2:p.Ser1293=
ENST00000663774.1:c.*4025C>T	ENSP00000499452.1:n.*4025C>T
ENST00000665872.1:c.*3948C>T	ENSP00000499600.1:n.*3948C>T
ENST00000666307.1:c.*4253C>T	ENSP00000499402.1:n.*4253C>T
ENST00000670063.1:c.*3984C>T	ENSP00000499725.1:n.*3984C>T
ENST00000302463.10:c.3585C>T	ENSP00000302028.6:p.Ser1195=
ENST00000399686.6:c.2722+485C>T
ENST00000402198.5:c.3879C>T	ENSP00000385852.1:p.Ser1293=
ENST00000406341.5:c.3879C>T	ENSP00000383939.1:p.Ser1293=
ENST00000407969.5:c.3936C>T	ENSP00000384114.1:p.Ser1312=
ENST00000413704.5:c.2915C>T
ENST00000459941.1:n.1010C>T
ENST00000466242.5:n.3220C>T
ENST00000466826.1:n.266C>T
ENST00000493918.5:n.4043C>T
NM_001080517.2:c.3879C>T	NP_001073986.1:p.Ser1293=
NM_001292043.1:c.3585C>T	NP_001278972.1:p.Ser1195=
XM_005265301.1:c.3936C>T	XP_005265358.1:p.Ser1312=
XM_005265303.1:c.3879C>T	XP_005265360.1:p.Ser1293=
XM_011533920.1:c.4053C>T	XP_011532222.1:p.Ser1351=
XM_011533921.1:c.4053C>T	XP_011532223.1:p.Ser1351=
XM_011533922.1:c.4032C>T	XP_011532224.1:p.Ser1344=
XM_011533923.1:c.4032C>T	XP_011532225.1:p.Ser1344=
XM_011533924.1:c.4032C>T	XP_011532226.1:p.Ser1344=
XM_011533925.1:c.4014C>T	XP_011532227.1:p.Ser1338=
XM_011533926.1:c.3996C>T	XP_011532228.1:p.Ser1332=
XM_011533927.1:c.3996C>T	XP_011532229.1:p.Ser1332=
XM_011533928.1:c.3975C>T	XP_011532230.1:p.Ser1325=
XM_011533929.1:c.3957C>T	XP_011532231.1:p.Ser1319=
XM_011533930.1:c.3918C>T	XP_011532232.1:p.Ser1306=
XM_011533931.1:c.3642C>T	XP_011532233.1:p.Ser1214=
XM_011533932.1:c.3603C>T	XP_011532234.1:p.Ser1201=
XM_011533933.1:c.3603C>T	XP_011532235.1:p.Ser1201=
NM_001349451.1:c.3585C>T	NP_001336380.1:p.Ser1195=
XM_011533921.2:c.4053C>T	XP_011532223.1:p.Ser1351=
XM_017006767.1:c.4053C>T	XP_016862256.1:p.Ser1351=
XM_017006768.2:c.4032C>T	XP_016862257.1:p.Ser1344=
XM_017006770.1:c.3996C>T	XP_016862259.1:p.Ser1332=
XM_017006771.1:c.3993C>T	XP_016862260.1:p.Ser1331=
XM_017006772.1:c.3957C>T	XP_016862261.1:p.Ser1319=
XM_017006773.1:c.3957C>T	XP_016862262.1:p.Ser1319=
XM_017006774.1:c.3936C>T	XP_016862263.1:p.Ser1312=
XM_017006775.1:c.3900C>T	XP_016862264.1:p.Ser1300=
XM_017006776.1:c.3642C>T	XP_016862265.1:p.Ser1214=
XM_017006777.1:c.3642C>T	XP_016862266.1:p.Ser1214=
XM_017006778.1:c.3642C>T	XP_016862267.1:p.Ser1214=
XM_017006779.1:c.3603C>T	XP_016862268.1:p.Ser1201=
XM_017006780.1:c.3603C>T	XP_016862269.1:p.Ser1201=
XM_017006783.1:c.3375C>T	XP_016862272.1:p.Ser1125=
XM_024453620.1:c.4014C>T	XP_024309388.1:p.Ser1338=
XM_024453621.1:c.3690C>T	XP_024309389.1:p.Ser1230=
XR_001740195.2:n.8262C>T
NM_001080517.3:c.3879C>T MANE Select	NP_001073986.1:p.Ser1293=
NM_001292043.2:c.3585C>T	NP_001278972.1:p.Ser1195=
NM_001349451.2:c.3585C>T	NP_001336380.1:p.Ser1195=