Canonical Allele Identifier: CA2406108635

Gene: EP300

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41160704A= , CM000684.2:g.41160704A=	GRCh38
NC_000022.10:g.41556708A= , CM000684.1:g.41556708A=	GRCh37
NC_000022.9:g.39886654A=	NCBI36
NG_009817.1:g.73095A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703544.1:c.*1573A=	ENSP00000515365.1:n.*1573A=
ENST00000263253.9:c.3653A= MANE Select	ENSP00000263253.7:p.Asp1218=
ENST00000674155.1:c.3575A=	ENSP00000501078.1:p.Asp1192=
ENST00000263253.8:c.3653A=	ENSP00000263253.7:p.Asp1218=
NM_001429.3:c.3653A=	NP_001420.2:p.Asp1218=
XM_006724165.2:c.3575A=	XP_006724228.1:p.Asp1192=
NM_001362843.1:c.3575A=	NP_001349772.1:p.Asp1192=
NM_001429.4:c.3653A= MANE Select	NP_001420.2:p.Asp1218=
NM_001362843.2:c.3575A=	NP_001349772.1:p.Asp1192=