Canonical Allele Identifier: CA2406108601

Gene: EP300

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41160609C= , CM000684.2:g.41160609C=	GRCh38
NC_000022.10:g.41556613C= , CM000684.1:g.41556613C=	GRCh37
NC_000022.9:g.39886559C=	NCBI36
NG_009817.1:g.73000C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703544.1:c.*1511-33C=	ENSP00000515365.1:n.*1511-33C=
ENST00000263253.9:c.3591-33C= MANE Select	ENSP00000263253.7:n.3591-33C=
ENST00000674155.1:c.3513-33C=	ENSP00000501078.1:n.3513-33C=
ENST00000263253.8:c.3591-33C=	ENSP00000263253.7:n.3591-33C=
NM_001429.3:c.3591-33C=	NP_001420.2:n.3591-33C=
XM_006724165.2:c.3513-33C=	XP_006724228.1:n.3513-33C=
NM_001362843.1:c.3513-33C=	NP_001349772.1:n.3513-33C=
NM_001429.4:c.3591-33C= MANE Select	NP_001420.2:n.3591-33C=
NM_001362843.2:c.3513-33C=	NP_001349772.1:n.3513-33C=