Canonical Allele Identifier: CA411693357

Gene: EP300

Linked Data

• dbSNP Id: rs746999540
• MyVariant Identifiers: chr22:g.41548296C>G (hg19) ; chr22:g.41152292C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41152292C>G , CM000684.2:g.41152292C>G	GRCh38
NC_000022.10:g.41548296C>G , CM000684.1:g.41548296C>G	GRCh37
NC_000022.9:g.39878242C>G	NCBI36
NG_009817.1:g.64683C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703544.1:c.*1004C>G	ENSP00000515365.1:n.*1004C>G
ENST00000703545.1:c.2874C>G
ENST00000263253.9:c.3084C>G MANE Select	ENSP00000263253.7:p.Asp1028Glu
ENST00000674155.1:c.3006C>G	ENSP00000501078.1:p.Asp1002Glu
ENST00000263253.8:c.3084C>G	ENSP00000263253.7:p.Asp1028Glu
NM_001429.3:c.3084C>G	NP_001420.2:p.Asp1028Glu
XM_006724165.2:c.3006C>G	XP_006724228.1:p.Asp1002Glu
NM_001362843.1:c.3006C>G	NP_001349772.1:p.Asp1002Glu
NM_001429.4:c.3084C>G MANE Select	NP_001420.2:p.Asp1028Glu
NM_001362843.2:c.3006C>G	NP_001349772.1:p.Asp1002Glu