Canonical Allele Identifier: CA394554554
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729022T>G , CM000678.2:g.3729022T>G GRCh38
NC_000016.9:g.3779023T>G , CM000678.1:g.3779023T>G GRCh37
NC_000016.8:g.3719024T>G NCBI36
NG_009873.1:g.156099A>C
NG_009873.2:g.156692A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6025A>C MANE Select ENSP00000262367.5:p.Ser2009Arg
ENST00000262367.9:c.6025A>C ENSP00000262367.5:p.Ser2009Arg
ENST00000382070.7:c.5911A>C ENSP00000371502.3:p.Ser1971Arg
NM_001079846.1:c.5911A>C NP_001073315.1:p.Ser1971Arg
NM_004380.2:c.6025A>C NP_004371.2:p.Ser2009Arg
XM_005255124.3:c.5980A>C XP_005255181.1:p.Ser1994Arg
XM_005255125.3:c.5608A>C XP_005255182.1:p.Ser1870Arg
XM_006720848.2:c.5764A>C XP_006720911.1:p.Ser1922Arg
XM_011522380.1:c.5971A>C XP_011520682.1:p.Ser1991Arg
XM_011522381.1:c.5272A>C XP_011520683.1:p.Ser1758Arg
XM_005255124.4:c.5980A>C XP_005255181.1:p.Ser1994Arg
XM_005255125.4:c.5608A>C XP_005255182.1:p.Ser1870Arg
XM_006720848.3:c.5764A>C XP_006720911.1:p.Ser1922Arg
XM_011522381.2:c.5272A>C XP_011520683.1:p.Ser1758Arg
XM_017022944.1:c.6019A>C XP_016878433.1:p.Ser2007Arg
NM_004380.3:c.6025A>C MANE Select NP_004371.2:p.Ser2009Arg