Canonical Allele Identifier: CA2202916449
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729560G= , CM000678.2:g.3729560G= GRCh38
NC_000016.9:g.3779561G= , CM000678.1:g.3779561G= GRCh37
NC_000016.8:g.3719562G= NCBI36
NG_009873.1:g.155561C=
NG_009873.2:g.156154C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5487C= MANE Select ENSP00000262367.5:p.His1829=
ENST00000262367.9:c.5487C= ENSP00000262367.5:p.His1829=
ENST00000382070.7:c.5373C= ENSP00000371502.3:p.His1791=
NM_001079846.1:c.5373C= NP_001073315.1:p.His1791=
NM_004380.2:c.5487C= NP_004371.2:p.His1829=
XM_005255124.3:c.5442C= XP_005255181.1:p.His1814=
XM_005255125.3:c.5070C= XP_005255182.1:p.His1690=
XM_006720848.2:c.5226C= XP_006720911.1:p.His1742=
XM_011522380.1:c.5433C= XP_011520682.1:p.His1811=
XM_011522381.1:c.4734C= XP_011520683.1:p.His1578=
XM_005255124.4:c.5442C= XP_005255181.1:p.His1814=
XM_005255125.4:c.5070C= XP_005255182.1:p.His1690=
XM_006720848.3:c.5226C= XP_006720911.1:p.His1742=
XM_011522381.2:c.4734C= XP_011520683.1:p.His1578=
XM_017022944.1:c.5481C= XP_016878433.1:p.His1827=
NM_004380.3:c.5487C= MANE Select NP_004371.2:p.His1829=