Canonical Allele Identifier: CA432528482

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9517451T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475767T>A , CM000665.2:g.9475767T>A	GRCh38
NC_000003.11:g.9517451T>A , CM000665.1:g.9517451T>A	GRCh37
NC_000003.10:g.9492451T>A	NCBI36
NG_034132.1:g.83068T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2960T>A
ENST00000682536.1:c.4101T>A	ENSP00000507956.1:p.Leu1367=
ENST00000687014.1:n.4994T>A
ENST00000689167.1:n.2385T>A
ENST00000693430.1:n.6247T>A
ENST00000402198.7:c.4005T>A MANE Select	ENSP00000385852.2:p.Leu1335=
ENST00000663774.1:c.*4151T>A	ENSP00000499452.1:n.*4151T>A
ENST00000665872.1:c.*4074T>A	ENSP00000499600.1:n.*4074T>A
ENST00000666307.1:c.*4379T>A	ENSP00000499402.1:n.*4379T>A
ENST00000670063.1:c.*4110T>A	ENSP00000499725.1:n.*4110T>A
ENST00000302463.10:c.3711T>A	ENSP00000302028.6:p.Leu1237=
ENST00000399686.6:c.2722+611T>A
ENST00000402198.5:c.4005T>A	ENSP00000385852.1:p.Leu1335=
ENST00000406341.5:c.4005T>A	ENSP00000383939.1:p.Leu1335=
ENST00000407969.5:c.4062T>A	ENSP00000384114.1:p.Leu1354=
ENST00000413704.5:c.3041T>A
ENST00000466242.5:n.3346T>A
ENST00000493918.5:n.4169T>A
NM_001080517.2:c.4005T>A	NP_001073986.1:p.Leu1335=
NM_001292043.1:c.3711T>A	NP_001278972.1:p.Leu1237=
XM_005265301.1:c.4062T>A	XP_005265358.1:p.Leu1354=
XM_005265303.1:c.4005T>A	XP_005265360.1:p.Leu1335=
XM_011533920.1:c.4179T>A	XP_011532222.1:p.Leu1393=
XM_011533921.1:c.4179T>A	XP_011532223.1:p.Leu1393=
XM_011533922.1:c.4158T>A	XP_011532224.1:p.Leu1386=
XM_011533923.1:c.4158T>A	XP_011532225.1:p.Leu1386=
XM_011533924.1:c.4158T>A	XP_011532226.1:p.Leu1386=
XM_011533925.1:c.4140T>A	XP_011532227.1:p.Leu1380=
XM_011533926.1:c.4122T>A	XP_011532228.1:p.Leu1374=
XM_011533927.1:c.4122T>A	XP_011532229.1:p.Leu1374=
XM_011533928.1:c.4101T>A	XP_011532230.1:p.Leu1367=
XM_011533929.1:c.4083T>A	XP_011532231.1:p.Leu1361=
XM_011533930.1:c.4044T>A	XP_011532232.1:p.Leu1348=
XM_011533931.1:c.3768T>A	XP_011532233.1:p.Leu1256=
XM_011533932.1:c.3729T>A	XP_011532234.1:p.Leu1243=
XM_011533933.1:c.3729T>A	XP_011532235.1:p.Leu1243=
NM_001349451.1:c.3711T>A	NP_001336380.1:p.Leu1237=
XM_011533921.2:c.4179T>A	XP_011532223.1:p.Leu1393=
XM_017006767.1:c.4179T>A	XP_016862256.1:p.Leu1393=
XM_017006768.2:c.4158T>A	XP_016862257.1:p.Leu1386=
XM_017006770.1:c.4122T>A	XP_016862259.1:p.Leu1374=
XM_017006771.1:c.4119T>A	XP_016862260.1:p.Leu1373=
XM_017006772.1:c.4083T>A	XP_016862261.1:p.Leu1361=
XM_017006773.1:c.4083T>A	XP_016862262.1:p.Leu1361=
XM_017006774.1:c.4062T>A	XP_016862263.1:p.Leu1354=
XM_017006775.1:c.4026T>A	XP_016862264.1:p.Leu1342=
XM_017006776.1:c.3768T>A	XP_016862265.1:p.Leu1256=
XM_017006777.1:c.3768T>A	XP_016862266.1:p.Leu1256=
XM_017006778.1:c.3768T>A	XP_016862267.1:p.Leu1256=
XM_017006779.1:c.3729T>A	XP_016862268.1:p.Leu1243=
XM_017006780.1:c.3729T>A	XP_016862269.1:p.Leu1243=
XM_017006783.1:c.3501T>A	XP_016862272.1:p.Leu1167=
XM_024453620.1:c.4140T>A	XP_024309388.1:p.Leu1380=
XM_024453621.1:c.3816T>A	XP_024309389.1:p.Leu1272=
XR_001740195.2:n.8388T>A
NM_001080517.3:c.4005T>A MANE Select	NP_001073986.1:p.Leu1335=
NM_001292043.2:c.3711T>A	NP_001278972.1:p.Leu1237=
NM_001349451.2:c.3711T>A	NP_001336380.1:p.Leu1237=