Canonical Allele Identifier: CA645616451
Gene: EP300 HGNC NCBI

Linked Data

COSMIC: COSM96430

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41160645_41162782del , CM000684.2:g.41160645_41162782del GRCh38
NC_000022.10:g.41556649_41558786del , CM000684.1:g.41556649_41558786del GRCh37
NC_000022.9:g.39886595_39888732del NCBI36
NG_009817.1:g.73036_75173del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703544.1:c.*1514_*1648+3del
ENST00000263253.9:c.3594_3728+3del
ENST00000674155.1:c.3516_3650+3del
ENST00000263253.8:c.3594_3728+3del
NM_001429.3:c.3594_3728+3del
XM_006724165.2:c.3516_3650+3del
NM_001362843.1:c.3516_3650+3del
NM_001429.4:c.3594_3728+3del
NM_001362843.2:c.3516_3650+3del