Canonical Allele Identifier: CA2737879897
Gene: EP300 HGNC NCBI

Linked Data

dbSNP Id: rs1341712082
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41160605G>C , CM000684.2:g.41160605G>C GRCh38
NC_000022.10:g.41556609G>C , CM000684.1:g.41556609G>C GRCh37
NC_000022.9:g.39886555G>C NCBI36
NG_009817.1:g.72996G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703544.1:c.*1511-37G>C ENSP00000515365.1:n.*1511-37G>C
ENST00000263253.9:c.3591-37G>C MANE Select ENSP00000263253.7:n.3591-37G>C
ENST00000674155.1:c.3513-37G>C ENSP00000501078.1:n.3513-37G>C
ENST00000263253.8:c.3591-37G>C ENSP00000263253.7:n.3591-37G>C
NM_001429.3:c.3591-37G>C NP_001420.2:n.3591-37G>C
XM_006724165.2:c.3513-37G>C XP_006724228.1:n.3513-37G>C
NM_001362843.1:c.3513-37G>C NP_001349772.1:n.3513-37G>C
NM_001429.4:c.3591-37G>C MANE Select NP_001420.2:n.3591-37G>C
NM_001362843.2:c.3513-37G>C NP_001349772.1:n.3513-37G>C
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