Canonical Allele Identifier: CA2202958541
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3777931G= , CM000678.2:g.3777931G= GRCh38
NC_000016.9:g.3827932G= , CM000678.1:g.3827932G= GRCh37
NC_000016.8:g.3767933G= NCBI36
NG_009873.1:g.107190C=
NG_009873.2:g.107783C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.2113+80C= MANE Select ENSP00000262367.5:n.2113+80C=
ENST00000262367.9:c.2113+80C= ENSP00000262367.5:n.2113+80C=
ENST00000382070.7:c.1999+80C= ENSP00000371502.3:n.1999+80C=
ENST00000570939.2:c.718+80C= ENSP00000461002.2:n.718+80C=
ENST00000571826.5:c.162+80C=
ENST00000572134.1:c.426+80C=
NM_001079846.1:c.1999+80C= NP_001073315.1:n.1999+80C=
NM_004380.2:c.2113+80C= NP_004371.2:n.2113+80C=
XM_005255124.3:c.2113+80C= XP_005255181.1:n.2113+80C=
XM_005255125.3:c.2113+80C= XP_005255182.1:n.2113+80C=
XM_006720848.2:c.2113+80C= XP_006720911.1:n.2113+80C=
XM_011522380.1:c.2059+80C= XP_011520682.1:n.2059+80C=
XM_011522381.1:c.1360+80C= XP_011520683.1:n.1360+80C=
XM_011522382.1:c.2113+80C= XP_011520684.1:n.2113+80C=
XM_005255124.4:c.2113+80C= XP_005255181.1:n.2113+80C=
XM_005255125.4:c.2113+80C= XP_005255182.1:n.2113+80C=
XM_006720848.3:c.2113+80C= XP_006720911.1:n.2113+80C=
XM_011522381.2:c.1360+80C= XP_011520683.1:n.1360+80C=
XM_011522382.3:c.2113+80C= XP_011520684.1:n.2113+80C=
XM_017022944.1:c.2113+80C= XP_016878433.1:n.2113+80C=
NM_004380.3:c.2113+80C= MANE Select NP_004371.2:n.2113+80C=