Canonical Allele Identifier: CA352526693

Gene: SETD2

Linked Data

• dbSNP Id: rs2106673782
• MyVariant Identifiers: chr3:g.47163756A>C (hg19) ; chr3:g.47122266A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47122266A>C , CM000665.2:g.47122266A>C	GRCh38
NC_000003.11:g.47163756A>C , CM000665.1:g.47163756A>C	GRCh37
NC_000003.10:g.47138760A>C	NCBI36
NG_032091.1:g.46712T>G , LRG_775:g.46712T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638947.2:c.2238T>G	ENSP00000491413.2:p.Asp746Glu
ENST00000685005.1:c.2271T>G	ENSP00000509568.1:p.Asp757Glu
ENST00000685399.1:c.250T>G
ENST00000685505.1:c.311T>G
ENST00000686773.1:c.250T>G
ENST00000688290.1:c.250T>G
ENST00000690461.1:c.534T>G	ENSP00000509352.1:p.Asp178Glu
ENST00000691544.1:c.72-24185T>G	ENSP00000510710.1:n.72-24185T>G
ENST00000692883.1:c.311T>G
ENST00000693321.1:c.250T>G
ENST00000409792.4:c.2370T>G MANE Select	ENSP00000386759.3:p.Asp790Glu
ENST00000330022.11:c.1985T>G
ENST00000409792.3:c.2370T>G	ENSP00000386759.3:p.Asp790Glu
ENST00000412450.1:c.2238T>G	ENSP00000416401.1:p.Asp746Glu
ENST00000431180.5:c.1522T>G
ENST00000445387.5:c.1270T>G
NM_014159.6:c.2370T>G , LRG_775t1:c.2370T>G	NP_054878.5:p.Asp790Glu
XM_011533631.1:c.2448T>G	XP_011531933.1:p.Asp816Glu
XM_011533632.1:c.2394T>G	XP_011531934.1:p.Asp798Glu
XM_011533633.1:c.2448T>G	XP_011531935.1:p.Asp816Glu
XM_011533634.1:c.2238T>G	XP_011531936.1:p.Asp746Glu
XR_940418.1:n.2463T>G
XR_940419.1:n.2551T>G
XR_940420.1:n.2551T>G
NM_001349370.1:c.2238T>G	NP_001336299.1:p.Asp746Glu
NR_146158.1:n.2423T>G
XM_011533632.3:c.2394T>G	XP_011531934.1:p.Asp798Glu
XM_024453487.1:c.2238T>G	XP_024309255.1:p.Asp746Glu
XM_024453488.1:c.2238T>G	XP_024309256.1:p.Asp746Glu
XM_024453489.1:c.2238T>G	XP_024309257.1:p.Asp746Glu
XR_001740131.2:n.2423T>G
XR_002959510.1:n.2299T>G
XR_002959511.1:n.2299T>G
XR_002959512.1:n.2299T>G
XR_002959513.1:n.2299T>G
XR_002959514.1:n.2299T>G
XR_002959515.1:n.2299T>G
XR_002959516.1:n.2299T>G
XR_002959517.1:n.2299T>G
NM_001349370.2:c.2238T>G	NP_001336299.1:p.Asp746Glu
NR_146158.2:n.2559T>G
NM_001349370.3:c.2238T>G	NP_001336299.1:p.Asp746Glu
NM_014159.7:c.2370T>G MANE Select	NP_054878.5:p.Asp790Glu
NR_146158.3:n.2559T>G