Canonical Allele Identifier: CA2202916478
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729656C= , CM000678.2:g.3729656C= GRCh38
NC_000016.9:g.3779657C= , CM000678.1:g.3779657C= GRCh37
NC_000016.8:g.3719658C= NCBI36
NG_009873.1:g.155465G=
NG_009873.2:g.156058G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5391G= MANE Select ENSP00000262367.5:p.Lys1797=
ENST00000262367.9:c.5391G= ENSP00000262367.5:p.Lys1797=
ENST00000382070.7:c.5277G= ENSP00000371502.3:p.Lys1759=
NM_001079846.1:c.5277G= NP_001073315.1:p.Lys1759=
NM_004380.2:c.5391G= NP_004371.2:p.Lys1797=
XM_005255124.3:c.5346G= XP_005255181.1:p.Lys1782=
XM_005255125.3:c.4974G= XP_005255182.1:p.Lys1658=
XM_006720848.2:c.5130G= XP_006720911.1:p.Lys1710=
XM_011522380.1:c.5337G= XP_011520682.1:p.Lys1779=
XM_011522381.1:c.4638G= XP_011520683.1:p.Lys1546=
XM_005255124.4:c.5346G= XP_005255181.1:p.Lys1782=
XM_005255125.4:c.4974G= XP_005255182.1:p.Lys1658=
XM_006720848.3:c.5130G= XP_006720911.1:p.Lys1710=
XM_011522381.2:c.4638G= XP_011520683.1:p.Lys1546=
XM_017022944.1:c.5385G= XP_016878433.1:p.Lys1795=
NM_004380.3:c.5391G= MANE Select NP_004371.2:p.Lys1797=