Canonical Allele Identifier: CA352556671

Gene: SETD2

Linked Data

• dbSNP Id: rs1064795661
• MyVariant Identifiers: chr3:g.47058745C>T (hg19) ; chr3:g.47017255C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47017255C>T , CM000665.2:g.47017255C>T	GRCh38
NC_000003.11:g.47058745C>T , CM000665.1:g.47058745C>T	GRCh37
NC_000003.10:g.47033749C>T	NCBI36
NG_032091.1:g.151723G>A , LRG_775:g.151723G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000638947.2:c.7402-1G>A	ENSP00000491413.2:n.7402-1G>A
ENST00000685005.1:c.7300-1G>A	ENSP00000509568.1:n.7300-1G>A
ENST00000685237.1:n.4343-1G>A
ENST00000685505.1:c.5858-1G>A
ENST00000686773.1:c.5697-1G>A
ENST00000686792.1:n.1756-1G>A
ENST00000686876.1:c.4250-1G>A
ENST00000687657.1:n.1753-1G>A
ENST00000688290.1:c.5373-1G>A
ENST00000690157.1:c.3887-1G>A
ENST00000690461.1:c.5822-1G>A	ENSP00000509352.1:n.5822-1G>A
ENST00000691544.1:c.2590-1G>A	ENSP00000510710.1:n.2590-1G>A
ENST00000691902.1:c.3329-1G>A
ENST00000692362.1:n.3463-1G>A
ENST00000692883.1:c.5939-1G>A
ENST00000693321.1:c.5793-1G>A
ENST00000693738.1:n.2975-1G>A
ENST00000409792.4:c.7534-1G>A MANE Select	ENSP00000386759.3:n.7534-1G>A
ENST00000330022.11:c.7354-1G>A
ENST00000409792.3:c.7534-1G>A	ENSP00000386759.3:n.7534-1G>A
ENST00000431180.5:c.6730-1G>A
ENST00000445387.5:c.6510-1G>A
NM_014159.6:c.7534-1G>A , LRG_775t1:c.7534-1G>A	NP_054878.5:n.7534-1G>A
XM_011533631.1:c.7612-1G>A	XP_011531933.1:n.7612-1G>A
XM_011533632.1:c.7558-1G>A	XP_011531934.1:n.7558-1G>A
XM_011533633.1:c.7477-1G>A	XP_011531935.1:n.7477-1G>A
XM_011533634.1:c.7402-1G>A	XP_011531936.1:n.7402-1G>A
XR_940418.1:n.7751-1G>A
NM_001349370.1:c.7402-1G>A	NP_001336299.1:n.7402-1G>A
NR_146158.1:n.7755-1G>A
XM_011533632.3:c.7558-1G>A	XP_011531934.1:n.7558-1G>A
XM_024453487.1:c.7267-1G>A	XP_024309255.1:n.7267-1G>A
XM_024453488.1:c.7102-1G>A	XP_024309256.1:n.7102-1G>A
XR_001740131.2:n.7570-1G>A
XR_002959510.1:n.7587-1G>A
XR_002959511.1:n.7746-1G>A
XR_002959512.1:n.7846-1G>A
XR_002959513.1:n.7680-1G>A
XR_002959515.1:n.7711-1G>A
NM_001349370.2:c.7402-1G>A	NP_001336299.1:n.7402-1G>A
NR_146158.2:n.7891-1G>A
NM_001349370.3:c.7402-1G>A	NP_001336299.1:n.7402-1G>A
NM_014159.7:c.7534-1G>A MANE Select	NP_054878.5:n.7534-1G>A
NR_146158.3:n.7891-1G>A