Canonical Allele Identifier: CA2656906795
Gene: EP300 HGNC NCBI

Linked Data

dbSNP Id: rs370701103

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41147787A>T , CM000684.2:g.41147787A>T GRCh38
NC_000022.10:g.41543791A>T , CM000684.1:g.41543791A>T GRCh37
NC_000022.9:g.39873737A>T NCBI36
NG_009817.1:g.60178A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703544.1:c.*52-50A>T ENSP00000515365.1:n.*52-50A>T
ENST00000703545.1:c.1922-50A>T
ENST00000263253.9:c.2132-50A>T MANE Select ENSP00000263253.7:n.2132-50A>T
ENST00000674155.1:c.2054-50A>T ENSP00000501078.1:n.2054-50A>T
ENST00000263253.8:c.2132-50A>T ENSP00000263253.7:n.2132-50A>T
ENST00000634728.1:c.176-50A>T ENSP00000488981.1:n.176-50A>T
ENST00000635538.1:n.265-50A>T
NM_001429.3:c.2132-50A>T NP_001420.2:n.2132-50A>T
XM_006724165.2:c.2054-50A>T XP_006724228.1:n.2054-50A>T
NM_001362843.1:c.2054-50A>T NP_001349772.1:n.2054-50A>T
NM_001429.4:c.2132-50A>T MANE Select NP_001420.2:n.2132-50A>T
NM_001362843.2:c.2054-50A>T NP_001349772.1:n.2054-50A>T