Canonical Allele Identifier: CA433602984

Gene: SETD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47124033T>C , CM000665.2:g.47124033T>C	GRCh38
NC_000003.11:g.47165523T>C , CM000665.1:g.47165523T>C	GRCh37
NC_000003.10:g.47140527T>C	NCBI36
NG_032091.1:g.44945A>G , LRG_775:g.44945A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014159.7:c.603A>G MANE Select	NP_054878.5:p.Thr201=
ENST00000409792.4:c.603A>G MANE Select	ENSP00000386759.3:p.Thr201=
NM_001349370.1:c.471A>G	NP_001336299.1:p.Thr157=
NM_001349370.2:c.471A>G	NP_001336299.1:p.Thr157=
NM_001349370.3:c.471A>G	NP_001336299.1:p.Thr157=
NM_014159.6:c.603A>G , LRG_775t1:c.603A>G	NP_054878.5:p.Thr201=
NR_146158.1:n.656A>G
NR_146158.2:n.792A>G
NR_146158.3:n.792A>G
ENST00000330022.11:c.218A>G
ENST00000409792.3:c.603A>G	ENSP00000386759.3:p.Thr201=
ENST00000412450.1:c.471A>G	ENSP00000416401.1:p.Thr157=
ENST00000638947.2:c.471A>G	ENSP00000491413.2:p.Thr157=
ENST00000685005.1:c.504A>G	ENSP00000509568.1:p.Thr168=
ENST00000691544.1:c.72-25952A>G	ENSP00000510710.1:n.72-25952A>G
XM_011533631.1:c.681A>G	XP_011531933.1:p.Thr227=
XM_011533632.1:c.627A>G	XP_011531934.1:p.Thr209=
XM_011533632.3:c.627A>G	XP_011531934.1:p.Thr209=
XM_011533633.1:c.681A>G	XP_011531935.1:p.Thr227=
XM_011533634.1:c.471A>G	XP_011531936.1:p.Thr157=
XM_024453487.1:c.471A>G	XP_024309255.1:p.Thr157=
XM_024453488.1:c.471A>G	XP_024309256.1:p.Thr157=
XM_024453489.1:c.471A>G	XP_024309257.1:p.Thr157=
XR_001740131.2:n.656A>G
XR_002959510.1:n.532A>G
XR_002959511.1:n.532A>G
XR_002959512.1:n.532A>G
XR_002959513.1:n.532A>G
XR_002959514.1:n.532A>G
XR_002959515.1:n.532A>G
XR_002959516.1:n.532A>G
XR_002959517.1:n.532A>G
XR_940418.1:n.696A>G
XR_940419.1:n.784A>G
XR_940420.1:n.784A>G