Canonical Allele Identifier: CA2202936603
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736702T= , CM000678.2:g.3736702T= GRCh38
NC_000016.9:g.3786703T= , CM000678.1:g.3786703T= GRCh37
NC_000016.8:g.3726704T= NCBI36
NG_009873.1:g.148419A=
NG_009873.2:g.149012A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4508A= MANE Select ENSP00000262367.5:p.Tyr1503=
ENST00000262367.9:c.4508A= ENSP00000262367.5:p.Tyr1503=
ENST00000382070.7:c.4394A= ENSP00000371502.3:p.Tyr1465=
ENST00000570939.2:c.3143A= ENSP00000461002.2:p.Tyr1048=
ENST00000571763.5:n.298A=
ENST00000574740.1:n.329A=
ENST00000576720.1:n.3331A=
NM_001079846.1:c.4394A= NP_001073315.1:p.Tyr1465=
NM_004380.2:c.4508A= NP_004371.2:p.Tyr1503=
XM_005255124.3:c.4463A= XP_005255181.1:p.Tyr1488=
XM_005255125.3:c.4091A= XP_005255182.1:p.Tyr1364=
XM_006720848.2:c.4247A= XP_006720911.1:p.Tyr1416=
XM_011522380.1:c.4454A= XP_011520682.1:p.Tyr1485=
XM_011522381.1:c.3755A= XP_011520683.1:p.Tyr1252=
XM_005255124.4:c.4463A= XP_005255181.1:p.Tyr1488=
XM_005255125.4:c.4091A= XP_005255182.1:p.Tyr1364=
XM_006720848.3:c.4247A= XP_006720911.1:p.Tyr1416=
XM_011522381.2:c.3755A= XP_011520683.1:p.Tyr1252=
XM_017022944.1:c.4502A= XP_016878433.1:p.Tyr1501=
NM_004380.3:c.4508A= MANE Select NP_004371.2:p.Tyr1503=