Canonical Allele Identifier: CA2202950916
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3770850G= , CM000678.2:g.3770850G= GRCh38
NC_000016.9:g.3820851G= , CM000678.1:g.3820851G= GRCh37
NC_000016.8:g.3760852G= NCBI36
NG_009873.1:g.114271C=
NG_009873.2:g.114864C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.2600C= MANE Select ENSP00000262367.5:p.Pro867=
ENST00000262367.9:c.2600C= ENSP00000262367.5:p.Pro867=
ENST00000382070.7:c.2486C= ENSP00000371502.3:p.Pro829=
ENST00000570939.2:c.1205C= ENSP00000461002.2:p.Pro402=
NM_001079846.1:c.2486C= NP_001073315.1:p.Pro829=
NM_004380.2:c.2600C= NP_004371.2:p.Pro867=
XM_005255124.3:c.2555C= XP_005255181.1:p.Pro852=
XM_005255125.3:c.2464-1497C= XP_005255182.1:n.2464-1497C=
XM_006720848.2:c.2600C= XP_006720911.1:p.Pro867=
XM_011522380.1:c.2546C= XP_011520682.1:p.Pro849=
XM_011522381.1:c.1847C= XP_011520683.1:p.Pro616=
XM_011522382.1:c.2600C= XP_011520684.1:p.Pro867=
XM_005255124.4:c.2555C= XP_005255181.1:p.Pro852=
XM_005255125.4:c.2464-1497C= XP_005255182.1:n.2464-1497C=
XM_006720848.3:c.2600C= XP_006720911.1:p.Pro867=
XM_011522381.2:c.1847C= XP_011520683.1:p.Pro616=
XM_011522382.3:c.2600C= XP_011520684.1:p.Pro867=
XM_017022944.1:c.2594C= XP_016878433.1:p.Pro865=
NM_004380.3:c.2600C= MANE Select NP_004371.2:p.Pro867=