Canonical Allele Identifier: CA2202916471

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729619G= , CM000678.2:g.3729619G=	GRCh38
NC_000016.9:g.3779620G= , CM000678.1:g.3779620G=	GRCh37
NC_000016.8:g.3719621G=	NCBI36
NG_009873.1:g.155502C=
NG_009873.2:g.156095C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5428C= MANE Select	ENSP00000262367.5:p.Arg1810=
ENST00000262367.9:c.5428C=	ENSP00000262367.5:p.Arg1810=
ENST00000382070.7:c.5314C=	ENSP00000371502.3:p.Arg1772=
NM_001079846.1:c.5314C=	NP_001073315.1:p.Arg1772=
NM_004380.2:c.5428C=	NP_004371.2:p.Arg1810=
XM_005255124.3:c.5383C=	XP_005255181.1:p.Arg1795=
XM_005255125.3:c.5011C=	XP_005255182.1:p.Arg1671=
XM_006720848.2:c.5167C=	XP_006720911.1:p.Arg1723=
XM_011522380.1:c.5374C=	XP_011520682.1:p.Arg1792=
XM_011522381.1:c.4675C=	XP_011520683.1:p.Arg1559=
XM_005255124.4:c.5383C=	XP_005255181.1:p.Arg1795=
XM_005255125.4:c.5011C=	XP_005255182.1:p.Arg1671=
XM_006720848.3:c.5167C=	XP_006720911.1:p.Arg1723=
XM_011522381.2:c.4675C=	XP_011520683.1:p.Arg1559=
XM_017022944.1:c.5422C=	XP_016878433.1:p.Arg1808=
NM_004380.3:c.5428C= MANE Select	NP_004371.2:p.Arg1810=