Canonical Allele Identifier: CA10252353

Gene: EP300

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41125906A>G , CM000684.2:g.41125906A>G	GRCh38
NC_000022.10:g.41521910A>G , CM000684.1:g.41521910A>G	GRCh37
NC_000022.9:g.39851856A>G	NCBI36
NG_009817.1:g.38297A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001429.4:c.772A>G MANE Select	NP_001420.2:p.Thr258Ala
ENST00000263253.9:c.772A>G MANE Select	ENSP00000263253.7:p.Thr258Ala
NM_001362843.1:c.772A>G	NP_001349772.1:p.Thr258Ala
NM_001362843.2:c.772A>G	NP_001349772.1:p.Thr258Ala
NM_001429.3:c.772A>G	NP_001420.2:p.Thr258Ala
ENST00000263253.8:c.772A>G	ENSP00000263253.7:p.Thr258Ala
ENST00000634787.1:n.94A>G
ENST00000634860.1:n.55A>G
ENST00000674155.1:c.772A>G	ENSP00000501078.1:p.Thr258Ala
ENST00000703544.1:c.772A>G	ENSP00000515365.1:p.Thr258Ala
ENST00000703545.1:c.656A>G
XM_006724165.2:c.772A>G	XP_006724228.1:p.Thr258Ala