Canonical Allele Identifier: CA2202916486

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729681T= , CM000678.2:g.3729681T=	GRCh38
NC_000016.9:g.3779682T= , CM000678.1:g.3779682T=	GRCh37
NC_000016.8:g.3719683T=	NCBI36
NG_009873.1:g.155440A=
NG_009873.2:g.156033A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004380.3:c.5366A= MANE Select	NP_004371.2:p.Asn1789=
ENST00000262367.10:c.5366A= MANE Select	ENSP00000262367.5:p.Asn1789=
NM_001079846.1:c.5252A=	NP_001073315.1:p.Asn1751=
NM_004380.2:c.5366A=	NP_004371.2:p.Asn1789=
ENST00000262367.9:c.5366A=	ENSP00000262367.5:p.Asn1789=
ENST00000382070.7:c.5252A=	ENSP00000371502.3:p.Asn1751=
XM_005255124.3:c.5321A=	XP_005255181.1:p.Asn1774=
XM_005255124.4:c.5321A=	XP_005255181.1:p.Asn1774=
XM_005255125.3:c.4949A=	XP_005255182.1:p.Asn1650=
XM_005255125.4:c.4949A=	XP_005255182.1:p.Asn1650=
XM_006720848.2:c.5105A=	XP_006720911.1:p.Asn1702=
XM_006720848.3:c.5105A=	XP_006720911.1:p.Asn1702=
XM_011522380.1:c.5312A=	XP_011520682.1:p.Asn1771=
XM_011522381.1:c.4613A=	XP_011520683.1:p.Asn1538=
XM_011522381.2:c.4613A=	XP_011520683.1:p.Asn1538=
XM_017022944.1:c.5360A=	XP_016878433.1:p.Asn1787=