Canonical Allele Identifier: CA2363224

Gene: SETD2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47120260C>T , CM000665.2:g.47120260C>T	GRCh38
NC_000003.11:g.47161750C>T , CM000665.1:g.47161750C>T	GRCh37
NC_000003.10:g.47136754C>T	NCBI36
NG_032091.1:g.48718G>A , LRG_775:g.48718G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638947.2:c.4244G>A	ENSP00000491413.2:p.Arg1415Gln
ENST00000685005.1:c.4277G>A	ENSP00000509568.1:p.Arg1426Gln
ENST00000685399.1:c.2256G>A
ENST00000685505.1:c.2317G>A
ENST00000686773.1:c.2256G>A
ENST00000686876.1:c.1392G>A
ENST00000688290.1:c.2256G>A
ENST00000690157.1:c.1392G>A
ENST00000690461.1:c.2540G>A	ENSP00000509352.1:p.Arg847Gln
ENST00000691544.1:c.72-22179G>A	ENSP00000510710.1:n.72-22179G>A
ENST00000691902.1:c.1392G>A
ENST00000692883.1:c.2317G>A
ENST00000693321.1:c.2256G>A
ENST00000409792.4:c.4376G>A MANE Select	ENSP00000386759.3:p.Arg1459Gln
ENST00000638947.1:c.26G>A	ENSP00000491413.1:p.Arg9Gln
ENST00000330022.11:c.3991G>A
ENST00000409792.3:c.4376G>A	ENSP00000386759.3:p.Arg1459Gln
ENST00000431180.5:c.3528G>A
ENST00000445387.5:c.3276G>A
NM_014159.6:c.4376G>A , LRG_775t1:c.4376G>A	NP_054878.5:p.Arg1459Gln
XM_011533631.1:c.4454G>A	XP_011531933.1:p.Arg1485Gln
XM_011533632.1:c.4400G>A	XP_011531934.1:p.Arg1467Gln
XM_011533633.1:c.4454G>A	XP_011531935.1:p.Arg1485Gln
XM_011533634.1:c.4244G>A	XP_011531936.1:p.Arg1415Gln
XR_940418.1:n.4469G>A
XR_940419.1:n.4557G>A
XR_940420.1:n.4557G>A
NM_001349370.1:c.4244G>A	NP_001336299.1:p.Arg1415Gln
NR_146158.1:n.4429G>A
XM_011533632.3:c.4400G>A	XP_011531934.1:p.Arg1467Gln
XM_024453487.1:c.4244G>A	XP_024309255.1:p.Arg1415Gln
XM_024453488.1:c.4244G>A	XP_024309256.1:p.Arg1415Gln
XM_024453489.1:c.4244G>A	XP_024309257.1:p.Arg1415Gln
XR_001740131.2:n.4429G>A
XR_002959510.1:n.4305G>A
XR_002959511.1:n.4305G>A
XR_002959512.1:n.4305G>A
XR_002959513.1:n.4305G>A
XR_002959514.1:n.4305G>A
XR_002959515.1:n.4305G>A
XR_002959516.1:n.4305G>A
XR_002959517.1:n.4305G>A
NM_001349370.2:c.4244G>A	NP_001336299.1:p.Arg1415Gln
NR_146158.2:n.4565G>A
NM_001349370.3:c.4244G>A	NP_001336299.1:p.Arg1415Gln
NM_014159.7:c.4376G>A MANE Select	NP_054878.5:p.Arg1459Gln
NR_146158.3:n.4565G>A