Canonical Allele Identifier: CA2202928872
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728840G= , CM000678.2:g.3728840G= GRCh38
NC_000016.9:g.3778841G= , CM000678.1:g.3778841G= GRCh37
NC_000016.8:g.3718842G= NCBI36
NG_009873.1:g.156281C=
NG_009873.2:g.156874C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.6207C= MANE Select ENSP00000262367.5:p.Asp2069=
ENST00000262367.9:c.6207C= ENSP00000262367.5:p.Asp2069=
ENST00000382070.7:c.6093C= ENSP00000371502.3:p.Asp2031=
NM_001079846.1:c.6093C= NP_001073315.1:p.Asp2031=
NM_004380.2:c.6207C= NP_004371.2:p.Asp2069=
XM_005255124.3:c.6162C= XP_005255181.1:p.Asp2054=
XM_005255125.3:c.5790C= XP_005255182.1:p.Asp1930=
XM_006720848.2:c.5946C= XP_006720911.1:p.Asp1982=
XM_011522380.1:c.6153C= XP_011520682.1:p.Asp2051=
XM_011522381.1:c.5454C= XP_011520683.1:p.Asp1818=
XM_005255124.4:c.6162C= XP_005255181.1:p.Asp2054=
XM_005255125.4:c.5790C= XP_005255182.1:p.Asp1930=
XM_006720848.3:c.5946C= XP_006720911.1:p.Asp1982=
XM_011522381.2:c.5454C= XP_011520683.1:p.Asp1818=
XM_017022944.1:c.6201C= XP_016878433.1:p.Asp2067=
NM_004380.3:c.6207C= MANE Select NP_004371.2:p.Asp2069=