Canonical Allele Identifier: CA2406108634

Gene: EP300

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41160700G= , CM000684.2:g.41160700G=	GRCh38
NC_000022.10:g.41556704G= , CM000684.1:g.41556704G=	GRCh37
NC_000022.9:g.39886650G=	NCBI36
NG_009817.1:g.73091G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703544.1:c.*1569G=	ENSP00000515365.1:n.*1569G=
ENST00000263253.9:c.3649G= MANE Select	ENSP00000263253.7:p.Asp1217=
ENST00000674155.1:c.3571G=	ENSP00000501078.1:p.Asp1191=
ENST00000263253.8:c.3649G=	ENSP00000263253.7:p.Asp1217=
NM_001429.3:c.3649G=	NP_001420.2:p.Asp1217=
XM_006724165.2:c.3571G=	XP_006724228.1:p.Asp1191=
NM_001362843.1:c.3571G=	NP_001349772.1:p.Asp1191=
NM_001429.4:c.3649G= MANE Select	NP_001420.2:p.Asp1217=
NM_001362843.2:c.3571G=	NP_001349772.1:p.Asp1191=