Canonical Allele Identifier: CA2202928842
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728752C= , CM000678.2:g.3728752C= GRCh38
NC_000016.9:g.3778753C= , CM000678.1:g.3778753C= GRCh37
NC_000016.8:g.3718754C= NCBI36
NG_009873.1:g.156369G=
NG_009873.2:g.156962G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6295G= MANE Select ENSP00000262367.5:p.Ala2099=
ENST00000262367.9:c.6295G= ENSP00000262367.5:p.Ala2099=
ENST00000382070.7:c.6181G= ENSP00000371502.3:p.Ala2061=
NM_001079846.1:c.6181G= NP_001073315.1:p.Ala2061=
NM_004380.2:c.6295G= NP_004371.2:p.Ala2099=
XM_005255124.3:c.6250G= XP_005255181.1:p.Ala2084=
XM_005255125.3:c.5878G= XP_005255182.1:p.Ala1960=
XM_006720848.2:c.6034G= XP_006720911.1:p.Ala2012=
XM_011522380.1:c.6241G= XP_011520682.1:p.Ala2081=
XM_011522381.1:c.5542G= XP_011520683.1:p.Ala1848=
XM_005255124.4:c.6250G= XP_005255181.1:p.Ala2084=
XM_005255125.4:c.5878G= XP_005255182.1:p.Ala1960=
XM_006720848.3:c.6034G= XP_006720911.1:p.Ala2012=
XM_011522381.2:c.5542G= XP_011520683.1:p.Ala1848=
XM_017022944.1:c.6289G= XP_016878433.1:p.Ala2097=
NM_004380.3:c.6295G= MANE Select NP_004371.2:p.Ala2099=