Canonical Allele Identifier: CA2202950927
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3770858A= , CM000678.2:g.3770858A= GRCh38
NC_000016.9:g.3820859A= , CM000678.1:g.3820859A= GRCh37
NC_000016.8:g.3760860A= NCBI36
NG_009873.1:g.114263T=
NG_009873.2:g.114856T=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.2592T= MANE Select ENSP00000262367.5:p.Ala864=
ENST00000262367.9:c.2592T= ENSP00000262367.5:p.Ala864=
ENST00000382070.7:c.2478T= ENSP00000371502.3:p.Ala826=
ENST00000570939.2:c.1197T= ENSP00000461002.2:p.Ala399=
NM_001079846.1:c.2478T= NP_001073315.1:p.Ala826=
NM_004380.2:c.2592T= NP_004371.2:p.Ala864=
XM_005255124.3:c.2547T= XP_005255181.1:p.Ala849=
XM_005255125.3:c.2464-1505T= XP_005255182.1:n.2464-1505T=
XM_006720848.2:c.2592T= XP_006720911.1:p.Ala864=
XM_011522380.1:c.2538T= XP_011520682.1:p.Ala846=
XM_011522381.1:c.1839T= XP_011520683.1:p.Ala613=
XM_011522382.1:c.2592T= XP_011520684.1:p.Ala864=
XM_005255124.4:c.2547T= XP_005255181.1:p.Ala849=
XM_005255125.4:c.2464-1505T= XP_005255182.1:n.2464-1505T=
XM_006720848.3:c.2592T= XP_006720911.1:p.Ala864=
XM_011522381.2:c.1839T= XP_011520683.1:p.Ala613=
XM_011522382.3:c.2592T= XP_011520684.1:p.Ala864=
XM_017022944.1:c.2586T= XP_016878433.1:p.Ala862=
NM_004380.3:c.2592T= MANE Select NP_004371.2:p.Ala864=