Canonical Allele Identifier: CA2202928831
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728722C= , CM000678.2:g.3728722C= GRCh38
NC_000016.9:g.3778723C= , CM000678.1:g.3778723C= GRCh37
NC_000016.8:g.3718724C= NCBI36
NG_009873.1:g.156399G=
NG_009873.2:g.156992G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6325G= MANE Select ENSP00000262367.5:p.Val2109=
ENST00000262367.9:c.6325G= ENSP00000262367.5:p.Val2109=
ENST00000382070.7:c.6211G= ENSP00000371502.3:p.Val2071=
NM_001079846.1:c.6211G= NP_001073315.1:p.Val2071=
NM_004380.2:c.6325G= NP_004371.2:p.Val2109=
XM_005255124.3:c.6280G= XP_005255181.1:p.Val2094=
XM_005255125.3:c.5908G= XP_005255182.1:p.Val1970=
XM_006720848.2:c.6064G= XP_006720911.1:p.Val2022=
XM_011522380.1:c.6271G= XP_011520682.1:p.Val2091=
XM_011522381.1:c.5572G= XP_011520683.1:p.Val1858=
XM_005255124.4:c.6280G= XP_005255181.1:p.Val2094=
XM_005255125.4:c.5908G= XP_005255182.1:p.Val1970=
XM_006720848.3:c.6064G= XP_006720911.1:p.Val2022=
XM_011522381.2:c.5572G= XP_011520683.1:p.Val1858=
XM_017022944.1:c.6319G= XP_016878433.1:p.Val2107=
NM_004380.3:c.6325G= MANE Select NP_004371.2:p.Val2109=