Canonical Allele Identifier: CA352526628

Gene: SETD2

Linked Data

• dbSNP Id: rs1025206273
• MyVariant Identifiers: chr3:g.47163739G>C (hg19) ; chr3:g.47122249G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47122249G>C , CM000665.2:g.47122249G>C	GRCh38
NC_000003.11:g.47163739G>C , CM000665.1:g.47163739G>C	GRCh37
NC_000003.10:g.47138743G>C	NCBI36
NG_032091.1:g.46729C>G , LRG_775:g.46729C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638947.2:c.2255C>G	ENSP00000491413.2:p.Thr752Ser
ENST00000685005.1:c.2288C>G	ENSP00000509568.1:p.Thr763Ser
ENST00000685399.1:c.267C>G
ENST00000685505.1:c.328C>G
ENST00000686773.1:c.267C>G
ENST00000688290.1:c.267C>G
ENST00000690461.1:c.551C>G	ENSP00000509352.1:p.Thr184Ser
ENST00000691544.1:c.72-24168C>G	ENSP00000510710.1:n.72-24168C>G
ENST00000692883.1:c.328C>G
ENST00000693321.1:c.267C>G
ENST00000409792.4:c.2387C>G MANE Select	ENSP00000386759.3:p.Thr796Ser
ENST00000330022.11:c.2002C>G
ENST00000409792.3:c.2387C>G	ENSP00000386759.3:p.Thr796Ser
ENST00000412450.1:c.2255C>G	ENSP00000416401.1:p.Thr752Ser
ENST00000431180.5:c.1539C>G
ENST00000445387.5:c.1287C>G
NM_014159.6:c.2387C>G , LRG_775t1:c.2387C>G	NP_054878.5:p.Thr796Ser
XM_011533631.1:c.2465C>G	XP_011531933.1:p.Thr822Ser
XM_011533632.1:c.2411C>G	XP_011531934.1:p.Thr804Ser
XM_011533633.1:c.2465C>G	XP_011531935.1:p.Thr822Ser
XM_011533634.1:c.2255C>G	XP_011531936.1:p.Thr752Ser
XR_940418.1:n.2480C>G
XR_940419.1:n.2568C>G
XR_940420.1:n.2568C>G
NM_001349370.1:c.2255C>G	NP_001336299.1:p.Thr752Ser
NR_146158.1:n.2440C>G
XM_011533632.3:c.2411C>G	XP_011531934.1:p.Thr804Ser
XM_024453487.1:c.2255C>G	XP_024309255.1:p.Thr752Ser
XM_024453488.1:c.2255C>G	XP_024309256.1:p.Thr752Ser
XM_024453489.1:c.2255C>G	XP_024309257.1:p.Thr752Ser
XR_001740131.2:n.2440C>G
XR_002959510.1:n.2316C>G
XR_002959511.1:n.2316C>G
XR_002959512.1:n.2316C>G
XR_002959513.1:n.2316C>G
XR_002959514.1:n.2316C>G
XR_002959515.1:n.2316C>G
XR_002959516.1:n.2316C>G
XR_002959517.1:n.2316C>G
NM_001349370.2:c.2255C>G	NP_001336299.1:p.Thr752Ser
NR_146158.2:n.2576C>G
NM_001349370.3:c.2255C>G	NP_001336299.1:p.Thr752Ser
NM_014159.7:c.2387C>G MANE Select	NP_054878.5:p.Thr796Ser
NR_146158.3:n.2576C>G