Canonical Allele Identifier: CA2202928361
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3727835T= , CM000678.2:g.3727835T= GRCh38
NC_000016.9:g.3777836T= , CM000678.1:g.3777836T= GRCh37
NC_000016.8:g.3717837T= NCBI36
NG_009873.1:g.157286A=
NG_009873.2:g.157879A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.7212A= MANE Select ENSP00000262367.5:p.Glu2404=
ENST00000262367.9:c.7212A= ENSP00000262367.5:p.Glu2404=
ENST00000382070.7:c.7098A= ENSP00000371502.3:p.Glu2366=
NM_001079846.1:c.7098A= NP_001073315.1:p.Glu2366=
NM_004380.2:c.7212A= NP_004371.2:p.Glu2404=
XM_005255124.3:c.7167A= XP_005255181.1:p.Glu2389=
XM_005255125.3:c.6795A= XP_005255182.1:p.Glu2265=
XM_006720848.2:c.6951A= XP_006720911.1:p.Glu2317=
XM_011522380.1:c.7158A= XP_011520682.1:p.Glu2386=
XM_011522381.1:c.6459A= XP_011520683.1:p.Glu2153=
XM_005255124.4:c.7167A= XP_005255181.1:p.Glu2389=
XM_005255125.4:c.6795A= XP_005255182.1:p.Glu2265=
XM_006720848.3:c.6951A= XP_006720911.1:p.Glu2317=
XM_011522381.2:c.6459A= XP_011520683.1:p.Glu2153=
XM_017022944.1:c.7206A= XP_016878433.1:p.Glu2402=
NM_004380.3:c.7212A= MANE Select NP_004371.2:p.Glu2404=