Canonical Allele Identifier: CA2406108653
Gene: EP300 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41160745A= , CM000684.2:g.41160745A= GRCh38
NC_000022.10:g.41556749A= , CM000684.1:g.41556749A= GRCh37
NC_000022.9:g.39886695A= NCBI36
NG_009817.1:g.73136A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703544.1:c.*1591+23A= ENSP00000515365.1:n.*1591+23A=
ENST00000263253.9:c.3671+23A= MANE Select ENSP00000263253.7:n.3671+23A=
ENST00000674155.1:c.3593+23A= ENSP00000501078.1:n.3593+23A=
ENST00000263253.8:c.3671+23A= ENSP00000263253.7:n.3671+23A=
NM_001429.3:c.3671+23A= NP_001420.2:n.3671+23A=
XM_006724165.2:c.3593+23A= XP_006724228.1:n.3593+23A=
NM_001362843.1:c.3593+23A= NP_001349772.1:n.3593+23A=
NM_001429.4:c.3671+23A= MANE Select NP_001420.2:n.3671+23A=
NM_001362843.2:c.3593+23A= NP_001349772.1:n.3593+23A=
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