Canonical Allele Identifier: CA394563866
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151329787

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736754A>T , CM000678.2:g.3736754A>T GRCh38
NC_000016.9:g.3786755A>T , CM000678.1:g.3786755A>T GRCh37
NC_000016.8:g.3726756A>T NCBI36
NG_009873.1:g.148367T>A
NG_009873.2:g.148960T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4456T>A MANE Select ENSP00000262367.5:p.Cys1486Ser
ENST00000262367.9:c.4456T>A ENSP00000262367.5:p.Cys1486Ser
ENST00000382070.7:c.4342T>A ENSP00000371502.3:p.Cys1448Ser
ENST00000570939.2:c.3091T>A ENSP00000461002.2:p.Cys1031Ser
ENST00000571763.5:n.246T>A
ENST00000574740.1:n.277T>A
ENST00000576720.1:n.3279T>A
NM_001079846.1:c.4342T>A NP_001073315.1:p.Cys1448Ser
NM_004380.2:c.4456T>A NP_004371.2:p.Cys1486Ser
XM_005255124.3:c.4411T>A XP_005255181.1:p.Cys1471Ser
XM_005255125.3:c.4039T>A XP_005255182.1:p.Cys1347Ser
XM_006720848.2:c.4195T>A XP_006720911.1:p.Cys1399Ser
XM_011522380.1:c.4402T>A XP_011520682.1:p.Cys1468Ser
XM_011522381.1:c.3703T>A XP_011520683.1:p.Cys1235Ser
XM_005255124.4:c.4411T>A XP_005255181.1:p.Cys1471Ser
XM_005255125.4:c.4039T>A XP_005255182.1:p.Cys1347Ser
XM_006720848.3:c.4195T>A XP_006720911.1:p.Cys1399Ser
XM_011522381.2:c.3703T>A XP_011520683.1:p.Cys1235Ser
XM_017022944.1:c.4450T>A XP_016878433.1:p.Cys1484Ser
NM_004380.3:c.4456T>A MANE Select NP_004371.2:p.Cys1486Ser