Canonical Allele Identifier: CA2202936648
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736729G= , CM000678.2:g.3736729G= GRCh38
NC_000016.9:g.3786730G= , CM000678.1:g.3786730G= GRCh37
NC_000016.8:g.3726731G= NCBI36
NG_009873.1:g.148392C=
NG_009873.2:g.148985C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.4481C= MANE Select ENSP00000262367.5:p.Pro1494=
ENST00000262367.9:c.4481C= ENSP00000262367.5:p.Pro1494=
ENST00000382070.7:c.4367C= ENSP00000371502.3:p.Pro1456=
ENST00000570939.2:c.3116C= ENSP00000461002.2:p.Pro1039=
ENST00000571763.5:n.271C=
ENST00000574740.1:n.302C=
ENST00000576720.1:n.3304C=
NM_001079846.1:c.4367C= NP_001073315.1:p.Pro1456=
NM_004380.2:c.4481C= NP_004371.2:p.Pro1494=
XM_005255124.3:c.4436C= XP_005255181.1:p.Pro1479=
XM_005255125.3:c.4064C= XP_005255182.1:p.Pro1355=
XM_006720848.2:c.4220C= XP_006720911.1:p.Pro1407=
XM_011522380.1:c.4427C= XP_011520682.1:p.Pro1476=
XM_011522381.1:c.3728C= XP_011520683.1:p.Pro1243=
XM_005255124.4:c.4436C= XP_005255181.1:p.Pro1479=
XM_005255125.4:c.4064C= XP_005255182.1:p.Pro1355=
XM_006720848.3:c.4220C= XP_006720911.1:p.Pro1407=
XM_011522381.2:c.3728C= XP_011520683.1:p.Pro1243=
XM_017022944.1:c.4475C= XP_016878433.1:p.Pro1492=
NM_004380.3:c.4481C= MANE Select NP_004371.2:p.Pro1494=