Canonical Allele Identifier: CA351693788

Gene: SETD5

Linked Data

• dbSNP Id: rs1166693724
• gnomAD v2: 3-9517468-C-T
• gnomAD v4: 3-9475784-C-T
• MyVariant Identifiers: chr3:g.9517468C>T (hg19) ; chr3:g.9475784C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475784C>T , CM000665.2:g.9475784C>T	GRCh38
NC_000003.11:g.9517468C>T , CM000665.1:g.9517468C>T	GRCh37
NC_000003.10:g.9492468C>T	NCBI36
NG_034132.1:g.83085C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2977C>T
ENST00000682536.1:c.4118C>T	ENSP00000507956.1:p.Pro1373Leu
ENST00000687014.1:n.5011C>T
ENST00000689167.1:n.2402C>T
ENST00000693430.1:n.6264C>T
ENST00000402198.7:c.4022C>T MANE Select	ENSP00000385852.2:p.Pro1341Leu
ENST00000663774.1:c.*4168C>T	ENSP00000499452.1:n.*4168C>T
ENST00000665872.1:c.*4091C>T	ENSP00000499600.1:n.*4091C>T
ENST00000666307.1:c.*4396C>T	ENSP00000499402.1:n.*4396C>T
ENST00000670063.1:c.*4127C>T	ENSP00000499725.1:n.*4127C>T
ENST00000302463.10:c.3728C>T	ENSP00000302028.6:p.Pro1243Leu
ENST00000399686.6:c.2722+628C>T
ENST00000402198.5:c.4022C>T	ENSP00000385852.1:p.Pro1341Leu
ENST00000406341.5:c.4022C>T	ENSP00000383939.1:p.Pro1341Leu
ENST00000407969.5:c.4079C>T	ENSP00000384114.1:p.Pro1360Leu
ENST00000413704.5:c.3058C>T
ENST00000466242.5:n.3363C>T
ENST00000493918.5:n.4186C>T
NM_001080517.2:c.4022C>T	NP_001073986.1:p.Pro1341Leu
NM_001292043.1:c.3728C>T	NP_001278972.1:p.Pro1243Leu
XM_005265301.1:c.4079C>T	XP_005265358.1:p.Pro1360Leu
XM_005265303.1:c.4022C>T	XP_005265360.1:p.Pro1341Leu
XM_011533920.1:c.4196C>T	XP_011532222.1:p.Pro1399Leu
XM_011533921.1:c.4196C>T	XP_011532223.1:p.Pro1399Leu
XM_011533922.1:c.4175C>T	XP_011532224.1:p.Pro1392Leu
XM_011533923.1:c.4175C>T	XP_011532225.1:p.Pro1392Leu
XM_011533924.1:c.4175C>T	XP_011532226.1:p.Pro1392Leu
XM_011533925.1:c.4157C>T	XP_011532227.1:p.Pro1386Leu
XM_011533926.1:c.4139C>T	XP_011532228.1:p.Pro1380Leu
XM_011533927.1:c.4139C>T	XP_011532229.1:p.Pro1380Leu
XM_011533928.1:c.4118C>T	XP_011532230.1:p.Pro1373Leu
XM_011533929.1:c.4100C>T	XP_011532231.1:p.Pro1367Leu
XM_011533930.1:c.4061C>T	XP_011532232.1:p.Pro1354Leu
XM_011533931.1:c.3785C>T	XP_011532233.1:p.Pro1262Leu
XM_011533932.1:c.3746C>T	XP_011532234.1:p.Pro1249Leu
XM_011533933.1:c.3746C>T	XP_011532235.1:p.Pro1249Leu
NM_001349451.1:c.3728C>T	NP_001336380.1:p.Pro1243Leu
XM_011533921.2:c.4196C>T	XP_011532223.1:p.Pro1399Leu
XM_017006767.1:c.4196C>T	XP_016862256.1:p.Pro1399Leu
XM_017006768.2:c.4175C>T	XP_016862257.1:p.Pro1392Leu
XM_017006770.1:c.4139C>T	XP_016862259.1:p.Pro1380Leu
XM_017006771.1:c.4136C>T	XP_016862260.1:p.Pro1379Leu
XM_017006772.1:c.4100C>T	XP_016862261.1:p.Pro1367Leu
XM_017006773.1:c.4100C>T	XP_016862262.1:p.Pro1367Leu
XM_017006774.1:c.4079C>T	XP_016862263.1:p.Pro1360Leu
XM_017006775.1:c.4043C>T	XP_016862264.1:p.Pro1348Leu
XM_017006776.1:c.3785C>T	XP_016862265.1:p.Pro1262Leu
XM_017006777.1:c.3785C>T	XP_016862266.1:p.Pro1262Leu
XM_017006778.1:c.3785C>T	XP_016862267.1:p.Pro1262Leu
XM_017006779.1:c.3746C>T	XP_016862268.1:p.Pro1249Leu
XM_017006780.1:c.3746C>T	XP_016862269.1:p.Pro1249Leu
XM_017006783.1:c.3518C>T	XP_016862272.1:p.Pro1173Leu
XM_024453620.1:c.4157C>T	XP_024309388.1:p.Pro1386Leu
XM_024453621.1:c.3833C>T	XP_024309389.1:p.Pro1278Leu
XR_001740195.2:n.8405C>T
NM_001080517.3:c.4022C>T MANE Select	NP_001073986.1:p.Pro1341Leu
NM_001292043.2:c.3728C>T	NP_001278972.1:p.Pro1243Leu
NM_001349451.2:c.3728C>T	NP_001336380.1:p.Pro1243Leu