Canonical Allele Identifier: CA2202971864
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3810728C= , CM000678.2:g.3810728C= GRCh38
NC_000016.9:g.3860729C= , CM000678.1:g.3860729C= GRCh37
NC_000016.8:g.3800730C= NCBI36
NG_009873.1:g.74393G=
NG_009873.2:g.74986G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.850G= MANE Select ENSP00000262367.5:p.Gly284=
ENST00000635899.1:n.92G=
ENST00000262367.9:c.850G= ENSP00000262367.5:p.Gly284=
ENST00000382070.7:c.850G= ENSP00000371502.3:p.Gly284=
NM_001079846.1:c.850G= NP_001073315.1:p.Gly284=
NM_004380.2:c.850G= NP_004371.2:p.Gly284=
XM_005255124.3:c.850G= XP_005255181.1:p.Gly284=
XM_005255125.3:c.850G= XP_005255182.1:p.Gly284=
XM_006720848.2:c.850G= XP_006720911.1:p.Gly284=
XM_011522380.1:c.796G= XP_011520682.1:p.Gly266=
XM_011522381.1:c.97G= XP_011520683.1:p.Gly33=
XM_011522382.1:c.850G= XP_011520684.1:p.Gly284=
XM_005255124.4:c.850G= XP_005255181.1:p.Gly284=
XM_005255125.4:c.850G= XP_005255182.1:p.Gly284=
XM_006720848.3:c.850G= XP_006720911.1:p.Gly284=
XM_011522381.2:c.97G= XP_011520683.1:p.Gly33=
XM_011522382.3:c.850G= XP_011520684.1:p.Gly284=
XM_017022944.1:c.850G= XP_016878433.1:p.Gly284=
NM_004380.3:c.850G= MANE Select NP_004371.2:p.Gly284=