Canonical Allele Identifier: CA2202958223
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3777653T= , CM000678.2:g.3777653T= GRCh38
NC_000016.9:g.3827654T= , CM000678.1:g.3827654T= GRCh37
NC_000016.8:g.3767655T= NCBI36
NG_009873.1:g.107468A=
NG_009873.2:g.108061A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.2118A= MANE Select ENSP00000262367.5:p.Gly706=
ENST00000262367.9:c.2118A= ENSP00000262367.5:p.Gly706=
ENST00000382070.7:c.2004A= ENSP00000371502.3:p.Gly668=
ENST00000570939.2:c.723A= ENSP00000461002.2:p.Gly241=
ENST00000571826.5:c.167A=
ENST00000572134.1:c.426+358A=
NM_001079846.1:c.2004A= NP_001073315.1:p.Gly668=
NM_004380.2:c.2118A= NP_004371.2:p.Gly706=
XM_005255124.3:c.2113+358A= XP_005255181.1:n.2113+358A=
XM_005255125.3:c.2118A= XP_005255182.1:p.Gly706=
XM_006720848.2:c.2118A= XP_006720911.1:p.Gly706=
XM_011522380.1:c.2064A= XP_011520682.1:p.Gly688=
XM_011522381.1:c.1365A= XP_011520683.1:p.Gly455=
XM_011522382.1:c.2118A= XP_011520684.1:p.Gly706=
XM_005255124.4:c.2113+358A= XP_005255181.1:n.2113+358A=
XM_005255125.4:c.2118A= XP_005255182.1:p.Gly706=
XM_006720848.3:c.2118A= XP_006720911.1:p.Gly706=
XM_011522381.2:c.1365A= XP_011520683.1:p.Gly455=
XM_011522382.3:c.2118A= XP_011520684.1:p.Gly706=
XM_017022944.1:c.2118A= XP_016878433.1:p.Gly706=
NM_004380.3:c.2118A= MANE Select NP_004371.2:p.Gly706=