Canonical Allele Identifier: CA2202916233

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729114T= , CM000678.2:g.3729114T=	GRCh38
NC_000016.9:g.3779115T= , CM000678.1:g.3779115T=	GRCh37
NC_000016.8:g.3719116T=	NCBI36
NG_009873.1:g.156007A=
NG_009873.2:g.156600A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5933A= MANE Select	ENSP00000262367.5:p.Asn1978=
ENST00000262367.9:c.5933A=	ENSP00000262367.5:p.Asn1978=
ENST00000382070.7:c.5819A=	ENSP00000371502.3:p.Asn1940=
NM_001079846.1:c.5819A=	NP_001073315.1:p.Asn1940=
NM_004380.2:c.5933A=	NP_004371.2:p.Asn1978=
XM_005255124.3:c.5888A=	XP_005255181.1:p.Asn1963=
XM_005255125.3:c.5516A=	XP_005255182.1:p.Asn1839=
XM_006720848.2:c.5672A=	XP_006720911.1:p.Asn1891=
XM_011522380.1:c.5879A=	XP_011520682.1:p.Asn1960=
XM_011522381.1:c.5180A=	XP_011520683.1:p.Asn1727=
XM_005255124.4:c.5888A=	XP_005255181.1:p.Asn1963=
XM_005255125.4:c.5516A=	XP_005255182.1:p.Asn1839=
XM_006720848.3:c.5672A=	XP_006720911.1:p.Asn1891=
XM_011522381.2:c.5180A=	XP_011520683.1:p.Asn1727=
XM_017022944.1:c.5927A=	XP_016878433.1:p.Asn1976=
NM_004380.3:c.5933A= MANE Select	NP_004371.2:p.Asn1978=