Canonical Allele Identifier: CA2202916150
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728992C= , CM000678.2:g.3728992C= GRCh38
NC_000016.9:g.3778993C= , CM000678.1:g.3778993C= GRCh37
NC_000016.8:g.3718994C= NCBI36
NG_009873.1:g.156129G=
NG_009873.2:g.156722G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6055G= MANE Select ENSP00000262367.5:p.Gly2019=
ENST00000262367.9:c.6055G= ENSP00000262367.5:p.Gly2019=
ENST00000382070.7:c.5941G= ENSP00000371502.3:p.Gly1981=
NM_001079846.1:c.5941G= NP_001073315.1:p.Gly1981=
NM_004380.2:c.6055G= NP_004371.2:p.Gly2019=
XM_005255124.3:c.6010G= XP_005255181.1:p.Gly2004=
XM_005255125.3:c.5638G= XP_005255182.1:p.Gly1880=
XM_006720848.2:c.5794G= XP_006720911.1:p.Gly1932=
XM_011522380.1:c.6001G= XP_011520682.1:p.Gly2001=
XM_011522381.1:c.5302G= XP_011520683.1:p.Gly1768=
XM_005255124.4:c.6010G= XP_005255181.1:p.Gly2004=
XM_005255125.4:c.5638G= XP_005255182.1:p.Gly1880=
XM_006720848.3:c.5794G= XP_006720911.1:p.Gly1932=
XM_011522381.2:c.5302G= XP_011520683.1:p.Gly1768=
XM_017022944.1:c.6049G= XP_016878433.1:p.Gly2017=
NM_004380.3:c.6055G= MANE Select NP_004371.2:p.Gly2019=