Canonical Allele Identifier: CA2239791

Gene: SETD5

Linked Data

• dbSNP Id: rs774302600
• ExAC: 3:9517179 G / A
• gnomAD v2: 3-9517179-G-A
• gnomAD v4: 3-9475495-G-A
• MyVariant Identifiers: chr3:g.9517179G>A (hg19) ; chr3:g.9475495G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475495G>A , CM000665.2:g.9475495G>A	GRCh38
NC_000003.11:g.9517179G>A , CM000665.1:g.9517179G>A	GRCh37
NC_000003.10:g.9492179G>A	NCBI36
NG_034132.1:g.82796G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2688G>A
ENST00000682536.1:c.3829G>A	ENSP00000507956.1:p.Asp1277Asn
ENST00000687014.1:n.4722G>A
ENST00000689167.1:n.2113G>A
ENST00000691925.1:n.6530G>A
ENST00000693430.1:n.5975G>A
ENST00000402198.7:c.3733G>A MANE Select	ENSP00000385852.2:p.Asp1245Asn
ENST00000663774.1:c.*3879G>A	ENSP00000499452.1:n.*3879G>A
ENST00000665872.1:c.*3802G>A	ENSP00000499600.1:n.*3802G>A
ENST00000666307.1:c.*4107G>A	ENSP00000499402.1:n.*4107G>A
ENST00000670063.1:c.*3838G>A	ENSP00000499725.1:n.*3838G>A
ENST00000302463.10:c.3439G>A	ENSP00000302028.6:p.Asp1147Asn
ENST00000399686.6:c.2722+339G>A
ENST00000402198.5:c.3733G>A	ENSP00000385852.1:p.Asp1245Asn
ENST00000406341.5:c.3733G>A	ENSP00000383939.1:p.Asp1245Asn
ENST00000407969.5:c.3790G>A	ENSP00000384114.1:p.Asp1264Asn
ENST00000413704.5:c.2769G>A
ENST00000459941.1:n.864G>A
ENST00000466242.5:n.3074G>A
ENST00000466826.1:n.120G>A
ENST00000493918.5:n.3897G>A
NM_001080517.2:c.3733G>A	NP_001073986.1:p.Asp1245Asn
NM_001292043.1:c.3439G>A	NP_001278972.1:p.Asp1147Asn
XM_005265301.1:c.3790G>A	XP_005265358.1:p.Asp1264Asn
XM_005265303.1:c.3733G>A	XP_005265360.1:p.Asp1245Asn
XM_011533920.1:c.3907G>A	XP_011532222.1:p.Asp1303Asn
XM_011533921.1:c.3907G>A	XP_011532223.1:p.Asp1303Asn
XM_011533922.1:c.3886G>A	XP_011532224.1:p.Asp1296Asn
XM_011533923.1:c.3886G>A	XP_011532225.1:p.Asp1296Asn
XM_011533924.1:c.3886G>A	XP_011532226.1:p.Asp1296Asn
XM_011533925.1:c.3868G>A	XP_011532227.1:p.Asp1290Asn
XM_011533926.1:c.3850G>A	XP_011532228.1:p.Asp1284Asn
XM_011533927.1:c.3850G>A	XP_011532229.1:p.Asp1284Asn
XM_011533928.1:c.3829G>A	XP_011532230.1:p.Asp1277Asn
XM_011533929.1:c.3811G>A	XP_011532231.1:p.Asp1271Asn
XM_011533930.1:c.3772G>A	XP_011532232.1:p.Asp1258Asn
XM_011533931.1:c.3496G>A	XP_011532233.1:p.Asp1166Asn
XM_011533932.1:c.3457G>A	XP_011532234.1:p.Asp1153Asn
XM_011533933.1:c.3457G>A	XP_011532235.1:p.Asp1153Asn
NM_001349451.1:c.3439G>A	NP_001336380.1:p.Asp1147Asn
XM_011533921.2:c.3907G>A	XP_011532223.1:p.Asp1303Asn
XM_017006767.1:c.3907G>A	XP_016862256.1:p.Asp1303Asn
XM_017006768.2:c.3886G>A	XP_016862257.1:p.Asp1296Asn
XM_017006770.1:c.3850G>A	XP_016862259.1:p.Asp1284Asn
XM_017006771.1:c.3847G>A	XP_016862260.1:p.Asp1283Asn
XM_017006772.1:c.3811G>A	XP_016862261.1:p.Asp1271Asn
XM_017006773.1:c.3811G>A	XP_016862262.1:p.Asp1271Asn
XM_017006774.1:c.3790G>A	XP_016862263.1:p.Asp1264Asn
XM_017006775.1:c.3754G>A	XP_016862264.1:p.Asp1252Asn
XM_017006776.1:c.3496G>A	XP_016862265.1:p.Asp1166Asn
XM_017006777.1:c.3496G>A	XP_016862266.1:p.Asp1166Asn
XM_017006778.1:c.3496G>A	XP_016862267.1:p.Asp1166Asn
XM_017006779.1:c.3457G>A	XP_016862268.1:p.Asp1153Asn
XM_017006780.1:c.3457G>A	XP_016862269.1:p.Asp1153Asn
XM_017006783.1:c.3229G>A	XP_016862272.1:p.Asp1077Asn
XM_024453620.1:c.3868G>A	XP_024309388.1:p.Asp1290Asn
XM_024453621.1:c.3544G>A	XP_024309389.1:p.Asp1182Asn
XR_001740195.2:n.8116G>A
NM_001080517.3:c.3733G>A MANE Select	NP_001073986.1:p.Asp1245Asn
NM_001292043.2:c.3439G>A	NP_001278972.1:p.Asp1147Asn
NM_001349451.2:c.3439G>A	NP_001336380.1:p.Asp1147Asn