Canonical Allele Identifier: CA432528604

Gene: SETD5

Linked Data

• dbSNP Id: rs1433379592
• gnomAD v3: 3-9475599-G-A
• gnomAD v4: 3-9475599-G-A
• MyVariant Identifiers: chr3:g.9517283G>A (hg19) ; chr3:g.9475599G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475599G>A , CM000665.2:g.9475599G>A	GRCh38
NC_000003.11:g.9517283G>A , CM000665.1:g.9517283G>A	GRCh37
NC_000003.10:g.9492283G>A	NCBI36
NG_034132.1:g.82900G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2792G>A
ENST00000682536.1:c.3933G>A	ENSP00000507956.1:p.Leu1311=
ENST00000687014.1:n.4826G>A
ENST00000689167.1:n.2217G>A
ENST00000691925.1:n.6634G>A
ENST00000693430.1:n.6079G>A
ENST00000402198.7:c.3837G>A MANE Select	ENSP00000385852.2:p.Leu1279=
ENST00000663774.1:c.*3983G>A	ENSP00000499452.1:n.*3983G>A
ENST00000665872.1:c.*3906G>A	ENSP00000499600.1:n.*3906G>A
ENST00000666307.1:c.*4211G>A	ENSP00000499402.1:n.*4211G>A
ENST00000670063.1:c.*3942G>A	ENSP00000499725.1:n.*3942G>A
ENST00000302463.10:c.3543G>A	ENSP00000302028.6:p.Leu1181=
ENST00000399686.6:c.2722+443G>A
ENST00000402198.5:c.3837G>A	ENSP00000385852.1:p.Leu1279=
ENST00000406341.5:c.3837G>A	ENSP00000383939.1:p.Leu1279=
ENST00000407969.5:c.3894G>A	ENSP00000384114.1:p.Leu1298=
ENST00000413704.5:c.2873G>A
ENST00000459941.1:n.968G>A
ENST00000466242.5:n.3178G>A
ENST00000466826.1:n.224G>A
ENST00000493918.5:n.4001G>A
NM_001080517.2:c.3837G>A	NP_001073986.1:p.Leu1279=
NM_001292043.1:c.3543G>A	NP_001278972.1:p.Leu1181=
XM_005265301.1:c.3894G>A	XP_005265358.1:p.Leu1298=
XM_005265303.1:c.3837G>A	XP_005265360.1:p.Leu1279=
XM_011533920.1:c.4011G>A	XP_011532222.1:p.Leu1337=
XM_011533921.1:c.4011G>A	XP_011532223.1:p.Leu1337=
XM_011533922.1:c.3990G>A	XP_011532224.1:p.Leu1330=
XM_011533923.1:c.3990G>A	XP_011532225.1:p.Leu1330=
XM_011533924.1:c.3990G>A	XP_011532226.1:p.Leu1330=
XM_011533925.1:c.3972G>A	XP_011532227.1:p.Leu1324=
XM_011533926.1:c.3954G>A	XP_011532228.1:p.Leu1318=
XM_011533927.1:c.3954G>A	XP_011532229.1:p.Leu1318=
XM_011533928.1:c.3933G>A	XP_011532230.1:p.Leu1311=
XM_011533929.1:c.3915G>A	XP_011532231.1:p.Leu1305=
XM_011533930.1:c.3876G>A	XP_011532232.1:p.Leu1292=
XM_011533931.1:c.3600G>A	XP_011532233.1:p.Leu1200=
XM_011533932.1:c.3561G>A	XP_011532234.1:p.Leu1187=
XM_011533933.1:c.3561G>A	XP_011532235.1:p.Leu1187=
NM_001349451.1:c.3543G>A	NP_001336380.1:p.Leu1181=
XM_011533921.2:c.4011G>A	XP_011532223.1:p.Leu1337=
XM_017006767.1:c.4011G>A	XP_016862256.1:p.Leu1337=
XM_017006768.2:c.3990G>A	XP_016862257.1:p.Leu1330=
XM_017006770.1:c.3954G>A	XP_016862259.1:p.Leu1318=
XM_017006771.1:c.3951G>A	XP_016862260.1:p.Leu1317=
XM_017006772.1:c.3915G>A	XP_016862261.1:p.Leu1305=
XM_017006773.1:c.3915G>A	XP_016862262.1:p.Leu1305=
XM_017006774.1:c.3894G>A	XP_016862263.1:p.Leu1298=
XM_017006775.1:c.3858G>A	XP_016862264.1:p.Leu1286=
XM_017006776.1:c.3600G>A	XP_016862265.1:p.Leu1200=
XM_017006777.1:c.3600G>A	XP_016862266.1:p.Leu1200=
XM_017006778.1:c.3600G>A	XP_016862267.1:p.Leu1200=
XM_017006779.1:c.3561G>A	XP_016862268.1:p.Leu1187=
XM_017006780.1:c.3561G>A	XP_016862269.1:p.Leu1187=
XM_017006783.1:c.3333G>A	XP_016862272.1:p.Leu1111=
XM_024453620.1:c.3972G>A	XP_024309388.1:p.Leu1324=
XM_024453621.1:c.3648G>A	XP_024309389.1:p.Leu1216=
XR_001740195.2:n.8220G>A
NM_001080517.3:c.3837G>A MANE Select	NP_001073986.1:p.Leu1279=
NM_001292043.2:c.3543G>A	NP_001278972.1:p.Leu1181=
NM_001349451.2:c.3543G>A	NP_001336380.1:p.Leu1181=