Canonical Allele Identifier: CA658796301

Gene: SETD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47056816G>C , CM000665.2:g.47056816G>C	GRCh38
NC_000003.11:g.47098306G>C , CM000665.1:g.47098306G>C	GRCh37
NC_000003.10:g.47073310G>C	NCBI36
NG_032091.1:g.112162C>G , LRG_775:g.112162C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638947.2:c.6831+5C>G	ENSP00000491413.2:n.6831+5C>G
ENST00000685005.1:c.6729+5C>G	ENSP00000509568.1:n.6729+5C>G
ENST00000685237.1:n.3772+5C>G
ENST00000685505.1:c.5287+5C>G
ENST00000686773.1:c.5126+5C>G
ENST00000686792.1:n.1185+5C>G
ENST00000686876.1:c.3679+5C>G
ENST00000687657.1:n.1182+5C>G
ENST00000688290.1:c.4802+5C>G
ENST00000690157.1:c.3316+5C>G
ENST00000690461.1:c.5127+5C>G	ENSP00000509352.1:n.5127+5C>G
ENST00000691544.1:c.2019+5C>G	ENSP00000510710.1:n.2019+5C>G
ENST00000691902.1:c.2758+5C>G
ENST00000692362.1:n.2768+5C>G
ENST00000692883.1:c.5287+5C>G
ENST00000693321.1:c.5222+5C>G
ENST00000693738.1:n.2404+5C>G
ENST00000409792.4:c.6963+5C>G MANE Select	ENSP00000386759.3:n.6963+5C>G
ENST00000330022.11:c.6783+5C>G
ENST00000409792.3:c.6963+5C>G	ENSP00000386759.3:n.6963+5C>G
ENST00000431180.5:c.6159+5C>G
ENST00000445387.5:c.5939+5C>G
NM_014159.6:c.6963+5C>G , LRG_775t1:c.6963+5C>G	NP_054878.5:n.6963+5C>G
XM_011533631.1:c.7041+5C>G	XP_011531933.1:n.7041+5C>G
XM_011533632.1:c.6987+5C>G	XP_011531934.1:n.6987+5C>G
XM_011533633.1:c.6906+5C>G	XP_011531935.1:n.6906+5C>G
XM_011533634.1:c.6831+5C>G	XP_011531936.1:n.6831+5C>G
XR_940418.1:n.7056+5C>G
NM_001349370.1:c.6831+5C>G	NP_001336299.1:n.6831+5C>G
NR_146158.1:n.7184+5C>G
XM_011533632.3:c.6987+5C>G	XP_011531934.1:n.6987+5C>G
XM_024453487.1:c.6696+5C>G	XP_024309255.1:n.6696+5C>G
XM_024453488.1:c.6531+5C>G	XP_024309256.1:n.6531+5C>G
XR_001740131.2:n.6999+5C>G
XR_002959510.1:n.6892+5C>G
XR_002959511.1:n.7175+5C>G
XR_002959512.1:n.7275+5C>G
XR_002959513.1:n.7109+5C>G
XR_002959515.1:n.7140+5C>G
NM_001349370.2:c.6831+5C>G	NP_001336299.1:n.6831+5C>G
NR_146158.2:n.7320+5C>G
NM_001349370.3:c.6831+5C>G	NP_001336299.1:n.6831+5C>G
NM_014159.7:c.6963+5C>G MANE Select	NP_054878.5:n.6963+5C>G
NR_146158.3:n.7320+5C>G