Canonical Allele Identifier: CA69951944

Gene: SETD5

Linked Data

• ClinVar Variation Id: 3058080
• ClinVar RCV Id: RCV003981828
• dbSNP Id: rs568748768
• gnomAD v3: 3-9475623-C-T
• gnomAD v4: 3-9475623-C-T
• MyVariant Identifiers: chr3:g.9517307C>T (hg19) ; chr3:g.9475623C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475623C>T , CM000665.2:g.9475623C>T	GRCh38
NC_000003.11:g.9517307C>T , CM000665.1:g.9517307C>T	GRCh37
NC_000003.10:g.9492307C>T	NCBI36
NG_034132.1:g.82924C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682236.1:n.2816C>T
ENST00000682536.1:c.3957C>T	ENSP00000507956.1:p.His1319=
ENST00000687014.1:n.4850C>T
ENST00000689167.1:n.2241C>T
ENST00000691925.1:n.6658C>T
ENST00000693430.1:n.6103C>T
ENST00000402198.7:c.3861C>T MANE Select	ENSP00000385852.2:p.His1287=
ENST00000663774.1:c.*4007C>T	ENSP00000499452.1:n.*4007C>T
ENST00000665872.1:c.*3930C>T	ENSP00000499600.1:n.*3930C>T
ENST00000666307.1:c.*4235C>T	ENSP00000499402.1:n.*4235C>T
ENST00000670063.1:c.*3966C>T	ENSP00000499725.1:n.*3966C>T
ENST00000302463.10:c.3567C>T	ENSP00000302028.6:p.His1189=
ENST00000399686.6:c.2722+467C>T
ENST00000402198.5:c.3861C>T	ENSP00000385852.1:p.His1287=
ENST00000406341.5:c.3861C>T	ENSP00000383939.1:p.His1287=
ENST00000407969.5:c.3918C>T	ENSP00000384114.1:p.His1306=
ENST00000413704.5:c.2897C>T
ENST00000459941.1:n.992C>T
ENST00000466242.5:n.3202C>T
ENST00000466826.1:n.248C>T
ENST00000493918.5:n.4025C>T
NM_001080517.2:c.3861C>T	NP_001073986.1:p.His1287=
NM_001292043.1:c.3567C>T	NP_001278972.1:p.His1189=
XM_005265301.1:c.3918C>T	XP_005265358.1:p.His1306=
XM_005265303.1:c.3861C>T	XP_005265360.1:p.His1287=
XM_011533920.1:c.4035C>T	XP_011532222.1:p.His1345=
XM_011533921.1:c.4035C>T	XP_011532223.1:p.His1345=
XM_011533922.1:c.4014C>T	XP_011532224.1:p.His1338=
XM_011533923.1:c.4014C>T	XP_011532225.1:p.His1338=
XM_011533924.1:c.4014C>T	XP_011532226.1:p.His1338=
XM_011533925.1:c.3996C>T	XP_011532227.1:p.His1332=
XM_011533926.1:c.3978C>T	XP_011532228.1:p.His1326=
XM_011533927.1:c.3978C>T	XP_011532229.1:p.His1326=
XM_011533928.1:c.3957C>T	XP_011532230.1:p.His1319=
XM_011533929.1:c.3939C>T	XP_011532231.1:p.His1313=
XM_011533930.1:c.3900C>T	XP_011532232.1:p.His1300=
XM_011533931.1:c.3624C>T	XP_011532233.1:p.His1208=
XM_011533932.1:c.3585C>T	XP_011532234.1:p.His1195=
XM_011533933.1:c.3585C>T	XP_011532235.1:p.His1195=
NM_001349451.1:c.3567C>T	NP_001336380.1:p.His1189=
XM_011533921.2:c.4035C>T	XP_011532223.1:p.His1345=
XM_017006767.1:c.4035C>T	XP_016862256.1:p.His1345=
XM_017006768.2:c.4014C>T	XP_016862257.1:p.His1338=
XM_017006770.1:c.3978C>T	XP_016862259.1:p.His1326=
XM_017006771.1:c.3975C>T	XP_016862260.1:p.His1325=
XM_017006772.1:c.3939C>T	XP_016862261.1:p.His1313=
XM_017006773.1:c.3939C>T	XP_016862262.1:p.His1313=
XM_017006774.1:c.3918C>T	XP_016862263.1:p.His1306=
XM_017006775.1:c.3882C>T	XP_016862264.1:p.His1294=
XM_017006776.1:c.3624C>T	XP_016862265.1:p.His1208=
XM_017006777.1:c.3624C>T	XP_016862266.1:p.His1208=
XM_017006778.1:c.3624C>T	XP_016862267.1:p.His1208=
XM_017006779.1:c.3585C>T	XP_016862268.1:p.His1195=
XM_017006780.1:c.3585C>T	XP_016862269.1:p.His1195=
XM_017006783.1:c.3357C>T	XP_016862272.1:p.His1119=
XM_024453620.1:c.3996C>T	XP_024309388.1:p.His1332=
XM_024453621.1:c.3672C>T	XP_024309389.1:p.His1224=
XR_001740195.2:n.8244C>T
NM_001080517.3:c.3861C>T MANE Select	NP_001073986.1:p.His1287=
NM_001292043.2:c.3567C>T	NP_001278972.1:p.His1189=
NM_001349451.2:c.3567C>T	NP_001336380.1:p.His1189=