Canonical Allele Identifier: CA2202958248
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3777667C= , CM000678.2:g.3777667C= GRCh38
NC_000016.9:g.3827668C= , CM000678.1:g.3827668C= GRCh37
NC_000016.8:g.3767669C= NCBI36
NG_009873.1:g.107454G=
NG_009873.2:g.108047G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.2114-10G= MANE Select ENSP00000262367.5:n.2114-10G=
ENST00000262367.9:c.2114-10G= ENSP00000262367.5:n.2114-10G=
ENST00000382070.7:c.2000-10G= ENSP00000371502.3:n.2000-10G=
ENST00000570939.2:c.719-10G= ENSP00000461002.2:n.719-10G=
ENST00000571826.5:c.163-10G=
ENST00000572134.1:c.426+344G=
NM_001079846.1:c.2000-10G= NP_001073315.1:n.2000-10G=
NM_004380.2:c.2114-10G= NP_004371.2:n.2114-10G=
XM_005255124.3:c.2113+344G= XP_005255181.1:n.2113+344G=
XM_005255125.3:c.2114-10G= XP_005255182.1:n.2114-10G=
XM_006720848.2:c.2114-10G= XP_006720911.1:n.2114-10G=
XM_011522380.1:c.2060-10G= XP_011520682.1:n.2060-10G=
XM_011522381.1:c.1361-10G= XP_011520683.1:n.1361-10G=
XM_011522382.1:c.2114-10G= XP_011520684.1:n.2114-10G=
XM_005255124.4:c.2113+344G= XP_005255181.1:n.2113+344G=
XM_005255125.4:c.2114-10G= XP_005255182.1:n.2114-10G=
XM_006720848.3:c.2114-10G= XP_006720911.1:n.2114-10G=
XM_011522381.2:c.1361-10G= XP_011520683.1:n.1361-10G=
XM_011522382.3:c.2114-10G= XP_011520684.1:n.2114-10G=
XM_017022944.1:c.2114-10G= XP_016878433.1:n.2114-10G=
NM_004380.3:c.2114-10G= MANE Select NP_004371.2:n.2114-10G=