Canonical Allele Identifier: CA2656906783
Gene: EP300 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41147769del , CM000684.2:g.41147769del GRCh38
NC_000022.10:g.41543773del , CM000684.1:g.41543773del GRCh37
NC_000022.9:g.39873719del NCBI36
NG_009817.1:g.60160del

Transcript Alleles

HGVS Amino-acid change
ENST00000703544.1:c.*52-68del ENSP00000515365.1:n.*52-68del
ENST00000703545.1:c.1922-68del
ENST00000263253.9:c.2132-68del MANE Select ENSP00000263253.7:n.2132-68del
ENST00000674155.1:c.2054-68del ENSP00000501078.1:n.2054-68del
ENST00000263253.8:c.2132-68del ENSP00000263253.7:n.2132-68del
ENST00000634728.1:c.176-68del ENSP00000488981.1:n.176-68del
ENST00000635538.1:n.265-68del
NM_001429.3:c.2132-68del NP_001420.2:n.2132-68del
XM_006724165.2:c.2054-68del XP_006724228.1:n.2054-68del
NM_001362843.1:c.2054-68del NP_001349772.1:n.2054-68del
NM_001429.4:c.2132-68del MANE Select NP_001420.2:n.2132-68del
NM_001362843.2:c.2054-68del NP_001349772.1:n.2054-68del