Canonical Allele Identifier: CA2202971878
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3810769G= , CM000678.2:g.3810769G= GRCh38
NC_000016.9:g.3860770G= , CM000678.1:g.3860770G= GRCh37
NC_000016.8:g.3800771G= NCBI36
NG_009873.1:g.74352C=
NG_009873.2:g.74945C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.809C= MANE Select ENSP00000262367.5:p.Thr270=
ENST00000635899.1:n.51C=
ENST00000262367.9:c.809C= ENSP00000262367.5:p.Thr270=
ENST00000382070.7:c.809C= ENSP00000371502.3:p.Thr270=
NM_001079846.1:c.809C= NP_001073315.1:p.Thr270=
NM_004380.2:c.809C= NP_004371.2:p.Thr270=
XM_005255124.3:c.809C= XP_005255181.1:p.Thr270=
XM_005255125.3:c.809C= XP_005255182.1:p.Thr270=
XM_006720848.2:c.809C= XP_006720911.1:p.Thr270=
XM_011522380.1:c.755C= XP_011520682.1:p.Thr252=
XM_011522381.1:c.56C= XP_011520683.1:p.Thr19=
XM_011522382.1:c.809C= XP_011520684.1:p.Thr270=
XM_005255124.4:c.809C= XP_005255181.1:p.Thr270=
XM_005255125.4:c.809C= XP_005255182.1:p.Thr270=
XM_006720848.3:c.809C= XP_006720911.1:p.Thr270=
XM_011522381.2:c.56C= XP_011520683.1:p.Thr19=
XM_011522382.3:c.809C= XP_011520684.1:p.Thr270=
XM_017022944.1:c.809C= XP_016878433.1:p.Thr270=
NM_004380.3:c.809C= MANE Select NP_004371.2:p.Thr270=