Canonical Allele Identifier: CA1362417969

Gene: SETD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47122186A= , CM000665.2:g.47122186A=	GRCh38
NC_000003.11:g.47163676A= , CM000665.1:g.47163676A=	GRCh37
NC_000003.10:g.47138680A=	NCBI36
NG_032091.1:g.46792T= , LRG_775:g.46792T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638947.2:c.2318T=	ENSP00000491413.2:p.Met773=
ENST00000685005.1:c.2351T=	ENSP00000509568.1:p.Met784=
ENST00000685399.1:c.330T=
ENST00000685505.1:c.391T=
ENST00000686773.1:c.330T=
ENST00000688290.1:c.330T=
ENST00000690461.1:c.614T=	ENSP00000509352.1:p.Met205=
ENST00000691544.1:c.72-24105T=	ENSP00000510710.1:n.72-24105T=
ENST00000692883.1:c.391T=
ENST00000693321.1:c.330T=
ENST00000409792.4:c.2450T= MANE Select	ENSP00000386759.3:p.Met817=
ENST00000330022.11:c.2065T=
ENST00000409792.3:c.2450T=	ENSP00000386759.3:p.Met817=
ENST00000412450.1:c.2318T=	ENSP00000416401.1:p.Met773=
ENST00000431180.5:c.1602T=
ENST00000445387.5:c.1350T=
NM_014159.6:c.2450T= , LRG_775t1:c.2450T=	NP_054878.5:p.Met817=
XM_011533631.1:c.2528T=	XP_011531933.1:p.Met843=
XM_011533632.1:c.2474T=	XP_011531934.1:p.Met825=
XM_011533633.1:c.2528T=	XP_011531935.1:p.Met843=
XM_011533634.1:c.2318T=	XP_011531936.1:p.Met773=
XR_940418.1:n.2543T=
XR_940419.1:n.2631T=
XR_940420.1:n.2631T=
NM_001349370.1:c.2318T=	NP_001336299.1:p.Met773=
NR_146158.1:n.2503T=
XM_011533632.3:c.2474T=	XP_011531934.1:p.Met825=
XM_024453487.1:c.2318T=	XP_024309255.1:p.Met773=
XM_024453488.1:c.2318T=	XP_024309256.1:p.Met773=
XM_024453489.1:c.2318T=	XP_024309257.1:p.Met773=
XR_001740131.2:n.2503T=
XR_002959510.1:n.2379T=
XR_002959511.1:n.2379T=
XR_002959512.1:n.2379T=
XR_002959513.1:n.2379T=
XR_002959514.1:n.2379T=
XR_002959515.1:n.2379T=
XR_002959516.1:n.2379T=
XR_002959517.1:n.2379T=
NM_001349370.2:c.2318T=	NP_001336299.1:p.Met773=
NR_146158.2:n.2639T=
NM_001349370.3:c.2318T=	NP_001336299.1:p.Met773=
NM_014159.7:c.2450T= MANE Select	NP_054878.5:p.Met817=
NR_146158.3:n.2639T=