Canonical Allele Identifier: CA2202916488

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729685C= , CM000678.2:g.3729685C=	GRCh38
NC_000016.9:g.3779686C= , CM000678.1:g.3779686C=	GRCh37
NC_000016.8:g.3719687C=	NCBI36
NG_009873.1:g.155436G=
NG_009873.2:g.156029G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5362G= MANE Select	ENSP00000262367.5:p.Ala1788=
ENST00000262367.9:c.5362G=	ENSP00000262367.5:p.Ala1788=
ENST00000382070.7:c.5248G=	ENSP00000371502.3:p.Ala1750=
NM_001079846.1:c.5248G=	NP_001073315.1:p.Ala1750=
NM_004380.2:c.5362G=	NP_004371.2:p.Ala1788=
XM_005255124.3:c.5317G=	XP_005255181.1:p.Ala1773=
XM_005255125.3:c.4945G=	XP_005255182.1:p.Ala1649=
XM_006720848.2:c.5101G=	XP_006720911.1:p.Ala1701=
XM_011522380.1:c.5308G=	XP_011520682.1:p.Ala1770=
XM_011522381.1:c.4609G=	XP_011520683.1:p.Ala1537=
XM_005255124.4:c.5317G=	XP_005255181.1:p.Ala1773=
XM_005255125.4:c.4945G=	XP_005255182.1:p.Ala1649=
XM_006720848.3:c.5101G=	XP_006720911.1:p.Ala1701=
XM_011522381.2:c.4609G=	XP_011520683.1:p.Ala1537=
XM_017022944.1:c.5356G=	XP_016878433.1:p.Ala1786=
NM_004380.3:c.5362G= MANE Select	NP_004371.2:p.Ala1788=