Canonical Allele Identifier: CA2656908335

Gene: EP300

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41146710A>C , CM000684.2:g.41146710A>C	GRCh38
NC_000022.10:g.41542714A>C , CM000684.1:g.41542714A>C	GRCh37
NC_000022.9:g.39872660A>C	NCBI36
NG_009817.1:g.59101A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703544.1:c.1879-29A>C	ENSP00000515365.1:n.1879-29A>C
ENST00000703545.1:c.1844-29A>C
ENST00000263253.9:c.2054-29A>C MANE Select	ENSP00000263253.7:n.2054-29A>C
ENST00000674155.1:c.2054-1127A>C	ENSP00000501078.1:n.2054-1127A>C
ENST00000263253.8:c.2054-29A>C	ENSP00000263253.7:n.2054-29A>C
ENST00000634690.1:c.489-29A>C
ENST00000634728.1:c.176-1127A>C	ENSP00000488981.1:n.176-1127A>C
ENST00000635538.1:n.158A>C
NM_001429.3:c.2054-29A>C	NP_001420.2:n.2054-29A>C
XM_006724165.2:c.2054-1127A>C	XP_006724228.1:n.2054-1127A>C
NM_001362843.1:c.2054-1127A>C	NP_001349772.1:n.2054-1127A>C
NM_001429.4:c.2054-29A>C MANE Select	NP_001420.2:n.2054-29A>C
NM_001362843.2:c.2054-1127A>C	NP_001349772.1:n.2054-1127A>C