Canonical Allele Identifier: CA2202916474

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729635G= , CM000678.2:g.3729635G=	GRCh38
NC_000016.9:g.3779636G= , CM000678.1:g.3779636G=	GRCh37
NC_000016.8:g.3719637G=	NCBI36
NG_009873.1:g.155486C=
NG_009873.2:g.156079C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5412C= MANE Select	ENSP00000262367.5:p.His1804=
ENST00000262367.9:c.5412C=	ENSP00000262367.5:p.His1804=
ENST00000382070.7:c.5298C=	ENSP00000371502.3:p.His1766=
NM_001079846.1:c.5298C=	NP_001073315.1:p.His1766=
NM_004380.2:c.5412C=	NP_004371.2:p.His1804=
XM_005255124.3:c.5367C=	XP_005255181.1:p.His1789=
XM_005255125.3:c.4995C=	XP_005255182.1:p.His1665=
XM_006720848.2:c.5151C=	XP_006720911.1:p.His1717=
XM_011522380.1:c.5358C=	XP_011520682.1:p.His1786=
XM_011522381.1:c.4659C=	XP_011520683.1:p.His1553=
XM_005255124.4:c.5367C=	XP_005255181.1:p.His1789=
XM_005255125.4:c.4995C=	XP_005255182.1:p.His1665=
XM_006720848.3:c.5151C=	XP_006720911.1:p.His1717=
XM_011522381.2:c.4659C=	XP_011520683.1:p.His1553=
XM_017022944.1:c.5406C=	XP_016878433.1:p.His1802=
NM_004380.3:c.5412C= MANE Select	NP_004371.2:p.His1804=