Canonical Allele Identifier: CA2202916433
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729500C= , CM000678.2:g.3729500C= GRCh38
NC_000016.9:g.3779501C= , CM000678.1:g.3779501C= GRCh37
NC_000016.8:g.3719502C= NCBI36
NG_009873.1:g.155621G=
NG_009873.2:g.156214G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5547G= MANE Select ENSP00000262367.5:p.Lys1849=
ENST00000262367.9:c.5547G= ENSP00000262367.5:p.Lys1849=
ENST00000382070.7:c.5433G= ENSP00000371502.3:p.Lys1811=
NM_001079846.1:c.5433G= NP_001073315.1:p.Lys1811=
NM_004380.2:c.5547G= NP_004371.2:p.Lys1849=
XM_005255124.3:c.5502G= XP_005255181.1:p.Lys1834=
XM_005255125.3:c.5130G= XP_005255182.1:p.Lys1710=
XM_006720848.2:c.5286G= XP_006720911.1:p.Lys1762=
XM_011522380.1:c.5493G= XP_011520682.1:p.Lys1831=
XM_011522381.1:c.4794G= XP_011520683.1:p.Lys1598=
XM_005255124.4:c.5502G= XP_005255181.1:p.Lys1834=
XM_005255125.4:c.5130G= XP_005255182.1:p.Lys1710=
XM_006720848.3:c.5286G= XP_006720911.1:p.Lys1762=
XM_011522381.2:c.4794G= XP_011520683.1:p.Lys1598=
XM_017022944.1:c.5541G= XP_016878433.1:p.Lys1847=
NM_004380.3:c.5547G= MANE Select NP_004371.2:p.Lys1849=