Canonical Allele Identifier: CA2203012444
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3879880T= , CM000678.2:g.3879880T= GRCh38
NC_000016.9:g.3929881T= , CM000678.1:g.3929881T= GRCh37
NC_000016.8:g.3869882T= NCBI36
NG_009873.1:g.5241A=
NG_009873.2:g.5834A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.37A= MANE Select ENSP00000262367.5:p.Lys13=
ENST00000262367.9:c.37A= ENSP00000262367.5:p.Lys13=
ENST00000382070.7:c.37A= ENSP00000371502.3:p.Lys13=
NM_001079846.1:c.37A= NP_001073315.1:p.Lys13=
NM_004380.2:c.37A= NP_004371.2:p.Lys13=
XM_005255124.3:c.37A= XP_005255181.1:p.Lys13=
XM_005255125.3:c.37A= XP_005255182.1:p.Lys13=
XM_006720848.2:c.37A= XP_006720911.1:p.Lys13=
XM_011522382.1:c.37A= XP_011520684.1:p.Lys13=
XM_005255124.4:c.37A= XP_005255181.1:p.Lys13=
XM_005255125.4:c.37A= XP_005255182.1:p.Lys13=
XM_006720848.3:c.37A= XP_006720911.1:p.Lys13=
XM_011522382.3:c.37A= XP_011520684.1:p.Lys13=
XM_017022944.1:c.37A= XP_016878433.1:p.Lys13=
NM_004380.3:c.37A= MANE Select NP_004371.2:p.Lys13=