Canonical Allele Identifier: CA2406108655
Gene: EP300 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41160748G= , CM000684.2:g.41160748G= GRCh38
NC_000022.10:g.41556752G= , CM000684.1:g.41556752G= GRCh37
NC_000022.9:g.39886698G= NCBI36
NG_009817.1:g.73139G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703544.1:c.*1591+26G= ENSP00000515365.1:n.*1591+26G=
ENST00000263253.9:c.3671+26G= MANE Select ENSP00000263253.7:n.3671+26G=
ENST00000674155.1:c.3593+26G= ENSP00000501078.1:n.3593+26G=
ENST00000263253.8:c.3671+26G= ENSP00000263253.7:n.3671+26G=
NM_001429.3:c.3671+26G= NP_001420.2:n.3671+26G=
XM_006724165.2:c.3593+26G= XP_006724228.1:n.3593+26G=
NM_001362843.1:c.3593+26G= NP_001349772.1:n.3593+26G=
NM_001429.4:c.3671+26G= MANE Select NP_001420.2:n.3671+26G=
NM_001362843.2:c.3593+26G= NP_001349772.1:n.3593+26G=
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