Canonical Allele Identifier: CA2202916566
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729851G= , CM000678.2:g.3729851G= GRCh38
NC_000016.9:g.3779852G= , CM000678.1:g.3779852G= GRCh37
NC_000016.8:g.3719853G= NCBI36
NG_009873.1:g.155270C=
NG_009873.2:g.155863C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5196C= MANE Select ENSP00000262367.5:p.Cys1732=
ENST00000262367.9:c.5196C= ENSP00000262367.5:p.Cys1732=
ENST00000382070.7:c.5082C= ENSP00000371502.3:p.Cys1694=
NM_001079846.1:c.5082C= NP_001073315.1:p.Cys1694=
NM_004380.2:c.5196C= NP_004371.2:p.Cys1732=
XM_005255124.3:c.5151C= XP_005255181.1:p.Cys1717=
XM_005255125.3:c.4779C= XP_005255182.1:p.Cys1593=
XM_006720848.2:c.4935C= XP_006720911.1:p.Cys1645=
XM_011522380.1:c.5142C= XP_011520682.1:p.Cys1714=
XM_011522381.1:c.4443C= XP_011520683.1:p.Cys1481=
XM_005255124.4:c.5151C= XP_005255181.1:p.Cys1717=
XM_005255125.4:c.4779C= XP_005255182.1:p.Cys1593=
XM_006720848.3:c.4935C= XP_006720911.1:p.Cys1645=
XM_011522381.2:c.4443C= XP_011520683.1:p.Cys1481=
XM_017022944.1:c.5190C= XP_016878433.1:p.Cys1730=
NM_004380.3:c.5196C= MANE Select NP_004371.2:p.Cys1732=