Canonical Allele Identifier: CA2202928846

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728768G= , CM000678.2:g.3728768G=	GRCh38
NC_000016.9:g.3778769G= , CM000678.1:g.3778769G=	GRCh37
NC_000016.8:g.3718770G=	NCBI36
NG_009873.1:g.156353C=
NG_009873.2:g.156946C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6279C= MANE Select	ENSP00000262367.5:p.Asn2093=
ENST00000262367.9:c.6279C=	ENSP00000262367.5:p.Asn2093=
ENST00000382070.7:c.6165C=	ENSP00000371502.3:p.Asn2055=
NM_001079846.1:c.6165C=	NP_001073315.1:p.Asn2055=
NM_004380.2:c.6279C=	NP_004371.2:p.Asn2093=
XM_005255124.3:c.6234C=	XP_005255181.1:p.Asn2078=
XM_005255125.3:c.5862C=	XP_005255182.1:p.Asn1954=
XM_006720848.2:c.6018C=	XP_006720911.1:p.Asn2006=
XM_011522380.1:c.6225C=	XP_011520682.1:p.Asn2075=
XM_011522381.1:c.5526C=	XP_011520683.1:p.Asn1842=
XM_005255124.4:c.6234C=	XP_005255181.1:p.Asn2078=
XM_005255125.4:c.5862C=	XP_005255182.1:p.Asn1954=
XM_006720848.3:c.6018C=	XP_006720911.1:p.Asn2006=
XM_011522381.2:c.5526C=	XP_011520683.1:p.Asn1842=
XM_017022944.1:c.6273C=	XP_016878433.1:p.Asn2091=
NM_004380.3:c.6279C= MANE Select	NP_004371.2:p.Asn2093=