Canonical Allele Identifier: CA2202958220

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3777652G= , CM000678.2:g.3777652G=	GRCh38
NC_000016.9:g.3827653G= , CM000678.1:g.3827653G=	GRCh37
NC_000016.8:g.3767654G=	NCBI36
NG_009873.1:g.107469C=
NG_009873.2:g.108062C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.2119C= MANE Select	ENSP00000262367.5:p.Pro707=
ENST00000262367.9:c.2119C=	ENSP00000262367.5:p.Pro707=
ENST00000382070.7:c.2005C=	ENSP00000371502.3:p.Pro669=
ENST00000570939.2:c.724C=	ENSP00000461002.2:p.Pro242=
ENST00000571826.5:c.168C=
ENST00000572134.1:c.426+359C=
NM_001079846.1:c.2005C=	NP_001073315.1:p.Pro669=
NM_004380.2:c.2119C=	NP_004371.2:p.Pro707=
XM_005255124.3:c.2113+359C=	XP_005255181.1:n.2113+359C=
XM_005255125.3:c.2119C=	XP_005255182.1:p.Pro707=
XM_006720848.2:c.2119C=	XP_006720911.1:p.Pro707=
XM_011522380.1:c.2065C=	XP_011520682.1:p.Pro689=
XM_011522381.1:c.1366C=	XP_011520683.1:p.Pro456=
XM_011522382.1:c.2119C=	XP_011520684.1:p.Pro707=
XM_005255124.4:c.2113+359C=	XP_005255181.1:n.2113+359C=
XM_005255125.4:c.2119C=	XP_005255182.1:p.Pro707=
XM_006720848.3:c.2119C=	XP_006720911.1:p.Pro707=
XM_011522381.2:c.1366C=	XP_011520683.1:p.Pro456=
XM_011522382.3:c.2119C=	XP_011520684.1:p.Pro707=
XM_017022944.1:c.2119C=	XP_016878433.1:p.Pro707=
NM_004380.3:c.2119C= MANE Select	NP_004371.2:p.Pro707=