Canonical Allele Identifier: CA2202936731
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736812A= , CM000678.2:g.3736812A= GRCh38
NC_000016.9:g.3786813A= , CM000678.1:g.3786813A= GRCh37
NC_000016.8:g.3726814A= NCBI36
NG_009873.1:g.148309T=
NG_009873.2:g.148902T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4398T= MANE Select ENSP00000262367.5:p.Tyr1466=
ENST00000262367.9:c.4398T= ENSP00000262367.5:p.Tyr1466=
ENST00000382070.7:c.4284T= ENSP00000371502.3:p.Tyr1428=
ENST00000570939.2:c.3033T= ENSP00000461002.2:p.Tyr1011=
ENST00000571763.5:n.188T=
ENST00000574740.1:n.219T=
ENST00000576720.1:n.3221T=
NM_001079846.1:c.4284T= NP_001073315.1:p.Tyr1428=
NM_004380.2:c.4398T= NP_004371.2:p.Tyr1466=
XM_005255124.3:c.4353T= XP_005255181.1:p.Tyr1451=
XM_005255125.3:c.3981T= XP_005255182.1:p.Tyr1327=
XM_006720848.2:c.4137T= XP_006720911.1:p.Tyr1379=
XM_011522380.1:c.4344T= XP_011520682.1:p.Tyr1448=
XM_011522381.1:c.3645T= XP_011520683.1:p.Tyr1215=
XM_005255124.4:c.4353T= XP_005255181.1:p.Tyr1451=
XM_005255125.4:c.3981T= XP_005255182.1:p.Tyr1327=
XM_006720848.3:c.4137T= XP_006720911.1:p.Tyr1379=
XM_011522381.2:c.3645T= XP_011520683.1:p.Tyr1215=
XM_017022944.1:c.4392T= XP_016878433.1:p.Tyr1464=
NM_004380.3:c.4398T= MANE Select NP_004371.2:p.Tyr1466=