Canonical Allele Identifier: CA10645617

Gene: EP300

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41179878_41179888delinsCCC , CM000684.2:g.41179878_41179888delinsCCC	GRCh38
NC_000022.10:g.41575882_41575892delinsCCC , CM000684.1:g.41575882_41575892delinsCCC	GRCh37
NC_000022.9:g.39905828_39905838delinsCCC	NCBI36
NG_009817.1:g.92269_92279delinsCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263253.9:c.*922_*932delinsCCC MANE Select	ENSP00000263253.7:n.*922_*932delinsCCC
ENST00000674155.1:c.8089_8099delinsCCC	ENSP00000501078.1:n.8089_8099delinsCCC
ENST00000263253.8:c.*922_*932delinsCCC	ENSP00000263253.7:n.*922_*932delinsCCC
NM_001429.3:c.*922_*932delinsCCC	NP_001420.2:n.*922_*932delinsCCC
XM_006724165.2:c.*922_*932delinsCCC	XP_006724228.1:n.*922_*932delinsCCC
NM_001362843.1:c.*922_*932delinsCCC	NP_001349772.1:n.*922_*932delinsCCC
NM_001429.4:c.*922_*932delinsCCC MANE Select	NP_001420.2:n.*922_*932delinsCCC
NM_001362843.2:c.*922_*932delinsCCC	NP_001349772.1:n.*922_*932delinsCCC