Canonical Allele Identifier: CA2202916184

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729046T= , CM000678.2:g.3729046T=	GRCh38
NC_000016.9:g.3779047T= , CM000678.1:g.3779047T=	GRCh37
NC_000016.8:g.3719048T=	NCBI36
NG_009873.1:g.156075A=
NG_009873.2:g.156668A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6001A= MANE Select	ENSP00000262367.5:p.Asn2001=
ENST00000262367.9:c.6001A=	ENSP00000262367.5:p.Asn2001=
ENST00000382070.7:c.5887A=	ENSP00000371502.3:p.Asn1963=
NM_001079846.1:c.5887A=	NP_001073315.1:p.Asn1963=
NM_004380.2:c.6001A=	NP_004371.2:p.Asn2001=
XM_005255124.3:c.5956A=	XP_005255181.1:p.Asn1986=
XM_005255125.3:c.5584A=	XP_005255182.1:p.Asn1862=
XM_006720848.2:c.5740A=	XP_006720911.1:p.Asn1914=
XM_011522380.1:c.5947A=	XP_011520682.1:p.Asn1983=
XM_011522381.1:c.5248A=	XP_011520683.1:p.Asn1750=
XM_005255124.4:c.5956A=	XP_005255181.1:p.Asn1986=
XM_005255125.4:c.5584A=	XP_005255182.1:p.Asn1862=
XM_006720848.3:c.5740A=	XP_006720911.1:p.Asn1914=
XM_011522381.2:c.5248A=	XP_011520683.1:p.Asn1750=
XM_017022944.1:c.5995A=	XP_016878433.1:p.Asn1999=
NM_004380.3:c.6001A= MANE Select	NP_004371.2:p.Asn2001=