Canonical Allele Identifier: CA2202928332
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3727773G= , CM000678.2:g.3727773G= GRCh38
NC_000016.9:g.3777774G= , CM000678.1:g.3777774G= GRCh37
NC_000016.8:g.3717775G= NCBI36
NG_009873.1:g.157348C=
NG_009873.2:g.157941C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.7274C= MANE Select ENSP00000262367.5:p.Ser2425=
ENST00000262367.9:c.7274C= ENSP00000262367.5:p.Ser2425=
ENST00000382070.7:c.7160C= ENSP00000371502.3:p.Ser2387=
NM_001079846.1:c.7160C= NP_001073315.1:p.Ser2387=
NM_004380.2:c.7274C= NP_004371.2:p.Ser2425=
XM_005255124.3:c.7229C= XP_005255181.1:p.Ser2410=
XM_005255125.3:c.6857C= XP_005255182.1:p.Ser2286=
XM_006720848.2:c.7013C= XP_006720911.1:p.Ser2338=
XM_011522380.1:c.7220C= XP_011520682.1:p.Ser2407=
XM_011522381.1:c.6521C= XP_011520683.1:p.Ser2174=
XM_005255124.4:c.7229C= XP_005255181.1:p.Ser2410=
XM_005255125.4:c.6857C= XP_005255182.1:p.Ser2286=
XM_006720848.3:c.7013C= XP_006720911.1:p.Ser2338=
XM_011522381.2:c.6521C= XP_011520683.1:p.Ser2174=
XM_017022944.1:c.7268C= XP_016878433.1:p.Ser2423=
NM_004380.3:c.7274C= MANE Select NP_004371.2:p.Ser2425=