Canonical Allele Identifier: CA2202916148

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728989G= , CM000678.2:g.3728989G=	GRCh38
NC_000016.9:g.3778990G= , CM000678.1:g.3778990G=	GRCh37
NC_000016.8:g.3718991G=	NCBI36
NG_009873.1:g.156132C=
NG_009873.2:g.156725C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6058C= MANE Select	ENSP00000262367.5:p.Gln2020=
ENST00000262367.9:c.6058C=	ENSP00000262367.5:p.Gln2020=
ENST00000382070.7:c.5944C=	ENSP00000371502.3:p.Gln1982=
NM_001079846.1:c.5944C=	NP_001073315.1:p.Gln1982=
NM_004380.2:c.6058C=	NP_004371.2:p.Gln2020=
XM_005255124.3:c.6013C=	XP_005255181.1:p.Gln2005=
XM_005255125.3:c.5641C=	XP_005255182.1:p.Gln1881=
XM_006720848.2:c.5797C=	XP_006720911.1:p.Gln1933=
XM_011522380.1:c.6004C=	XP_011520682.1:p.Gln2002=
XM_011522381.1:c.5305C=	XP_011520683.1:p.Gln1769=
XM_005255124.4:c.6013C=	XP_005255181.1:p.Gln2005=
XM_005255125.4:c.5641C=	XP_005255182.1:p.Gln1881=
XM_006720848.3:c.5797C=	XP_006720911.1:p.Gln1933=
XM_011522381.2:c.5305C=	XP_011520683.1:p.Gln1769=
XM_017022944.1:c.6052C=	XP_016878433.1:p.Gln2018=
NM_004380.3:c.6058C= MANE Select	NP_004371.2:p.Gln2020=