Canonical Allele Identifier: CA2363615
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 542227
dbSNP Id: rs145650484
gnomAD v2: 3-47164241-T-C
gnomAD v3: 3-47122751-T-C
gnomAD v4: 3-47122751-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47122751T>C , CM000665.2:g.47122751T>C GRCh38
NC_000003.11:g.47164241T>C , CM000665.1:g.47164241T>C GRCh37
NC_000003.10:g.47139245T>C NCBI36
NG_032091.1:g.46227A>G , LRG_775:g.46227A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000638947.2:c.1753A>G ENSP00000491413.2:p.Lys585Glu
ENST00000685005.1:c.1786A>G ENSP00000509568.1:p.Lys596Glu
ENST00000690461.1:c.49A>G ENSP00000509352.1:p.Lys17Glu
ENST00000691544.1:c.72-24670A>G ENSP00000510710.1:n.72-24670A>G
ENST00000409792.4:c.1885A>G MANE Select ENSP00000386759.3:p.Lys629Glu
ENST00000330022.11:c.1500A>G
ENST00000409792.3:c.1885A>G ENSP00000386759.3:p.Lys629Glu
ENST00000412450.1:c.1753A>G ENSP00000416401.1:p.Lys585Glu
ENST00000431180.5:c.1037A>G
ENST00000445387.5:c.785A>G
NM_014159.6:c.1885A>G , LRG_775t1:c.1885A>G NP_054878.5:p.Lys629Glu
XM_011533631.1:c.1963A>G XP_011531933.1:p.Lys655Glu
XM_011533632.1:c.1909A>G XP_011531934.1:p.Lys637Glu
XM_011533633.1:c.1963A>G XP_011531935.1:p.Lys655Glu
XM_011533634.1:c.1753A>G XP_011531936.1:p.Lys585Glu
XR_940418.1:n.1978A>G
XR_940419.1:n.2066A>G
XR_940420.1:n.2066A>G
NM_001349370.1:c.1753A>G NP_001336299.1:p.Lys585Glu
NR_146158.1:n.1938A>G
XM_011533632.3:c.1909A>G XP_011531934.1:p.Lys637Glu
XM_024453487.1:c.1753A>G XP_024309255.1:p.Lys585Glu
XM_024453488.1:c.1753A>G XP_024309256.1:p.Lys585Glu
XM_024453489.1:c.1753A>G XP_024309257.1:p.Lys585Glu
XR_001740131.2:n.1938A>G
XR_002959510.1:n.1814A>G
XR_002959511.1:n.1814A>G
XR_002959512.1:n.1814A>G
XR_002959513.1:n.1814A>G
XR_002959514.1:n.1814A>G
XR_002959515.1:n.1814A>G
XR_002959516.1:n.1814A>G
XR_002959517.1:n.1814A>G
NM_001349370.2:c.1753A>G NP_001336299.1:p.Lys585Glu
NR_146158.2:n.2074A>G
NM_001349370.3:c.1753A>G NP_001336299.1:p.Lys585Glu
NM_014159.7:c.1885A>G MANE Select NP_054878.5:p.Lys629Glu
NR_146158.3:n.2074A>G