Canonical Allele Identifier: CA2737986471
Gene: EP300 HGNC NCBI

Linked Data

dbSNP Id: rs2145752215
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41160612T>A , CM000684.2:g.41160612T>A GRCh38
NC_000022.10:g.41556616T>A , CM000684.1:g.41556616T>A GRCh37
NC_000022.9:g.39886562T>A NCBI36
NG_009817.1:g.73003T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703544.1:c.*1511-30T>A ENSP00000515365.1:n.*1511-30T>A
ENST00000263253.9:c.3591-30T>A MANE Select ENSP00000263253.7:n.3591-30T>A
ENST00000674155.1:c.3513-30T>A ENSP00000501078.1:n.3513-30T>A
ENST00000263253.8:c.3591-30T>A ENSP00000263253.7:n.3591-30T>A
NM_001429.3:c.3591-30T>A NP_001420.2:n.3591-30T>A
XM_006724165.2:c.3513-30T>A XP_006724228.1:n.3513-30T>A
NM_001362843.1:c.3513-30T>A NP_001349772.1:n.3513-30T>A
NM_001429.4:c.3591-30T>A MANE Select NP_001420.2:n.3591-30T>A
NM_001362843.2:c.3513-30T>A NP_001349772.1:n.3513-30T>A
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