Canonical Allele Identifier: CA2363707

Gene: SETD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47123456A>G , CM000665.2:g.47123456A>G	GRCh38
NC_000003.11:g.47164946A>G , CM000665.1:g.47164946A>G	GRCh37
NC_000003.10:g.47139950A>G	NCBI36
NG_032091.1:g.45522T>C , LRG_775:g.45522T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014159.7:c.1180T>C MANE Select	NP_054878.5:p.Cys394Arg
ENST00000409792.4:c.1180T>C MANE Select	ENSP00000386759.3:p.Cys394Arg
NM_001349370.1:c.1048T>C	NP_001336299.1:p.Cys350Arg
NM_001349370.2:c.1048T>C	NP_001336299.1:p.Cys350Arg
NM_001349370.3:c.1048T>C	NP_001336299.1:p.Cys350Arg
NM_014159.6:c.1180T>C , LRG_775t1:c.1180T>C	NP_054878.5:p.Cys394Arg
NR_146158.1:n.1233T>C
NR_146158.2:n.1369T>C
NR_146158.3:n.1369T>C
ENST00000330022.11:c.795T>C
ENST00000409792.3:c.1180T>C	ENSP00000386759.3:p.Cys394Arg
ENST00000412450.1:c.1048T>C	ENSP00000416401.1:p.Cys350Arg
ENST00000431180.5:c.332T>C
ENST00000445387.5:c.80T>C
ENST00000638947.2:c.1048T>C	ENSP00000491413.2:p.Cys350Arg
ENST00000685005.1:c.1081T>C	ENSP00000509568.1:p.Cys361Arg
ENST00000691544.1:c.72-25375T>C	ENSP00000510710.1:n.72-25375T>C
XM_011533631.1:c.1258T>C	XP_011531933.1:p.Cys420Arg
XM_011533632.1:c.1204T>C	XP_011531934.1:p.Cys402Arg
XM_011533632.3:c.1204T>C	XP_011531934.1:p.Cys402Arg
XM_011533633.1:c.1258T>C	XP_011531935.1:p.Cys420Arg
XM_011533634.1:c.1048T>C	XP_011531936.1:p.Cys350Arg
XM_024453487.1:c.1048T>C	XP_024309255.1:p.Cys350Arg
XM_024453488.1:c.1048T>C	XP_024309256.1:p.Cys350Arg
XM_024453489.1:c.1048T>C	XP_024309257.1:p.Cys350Arg
XR_001740131.2:n.1233T>C
XR_002959510.1:n.1109T>C
XR_002959511.1:n.1109T>C
XR_002959512.1:n.1109T>C
XR_002959513.1:n.1109T>C
XR_002959514.1:n.1109T>C
XR_002959515.1:n.1109T>C
XR_002959516.1:n.1109T>C
XR_002959517.1:n.1109T>C
XR_940418.1:n.1273T>C
XR_940419.1:n.1361T>C
XR_940420.1:n.1361T>C