Canonical Allele Identifier: CA2202916136

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728960C= , CM000678.2:g.3728960C=	GRCh38
NC_000016.9:g.3778961C= , CM000678.1:g.3778961C=	GRCh37
NC_000016.8:g.3718962C=	NCBI36
NG_009873.1:g.156161G=
NG_009873.2:g.156754G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6087G= MANE Select	ENSP00000262367.5:p.Gln2029=
ENST00000262367.9:c.6087G=	ENSP00000262367.5:p.Gln2029=
ENST00000382070.7:c.5973G=	ENSP00000371502.3:p.Gln1991=
NM_001079846.1:c.5973G=	NP_001073315.1:p.Gln1991=
NM_004380.2:c.6087G=	NP_004371.2:p.Gln2029=
XM_005255124.3:c.6042G=	XP_005255181.1:p.Gln2014=
XM_005255125.3:c.5670G=	XP_005255182.1:p.Gln1890=
XM_006720848.2:c.5826G=	XP_006720911.1:p.Gln1942=
XM_011522380.1:c.6033G=	XP_011520682.1:p.Gln2011=
XM_011522381.1:c.5334G=	XP_011520683.1:p.Gln1778=
XM_005255124.4:c.6042G=	XP_005255181.1:p.Gln2014=
XM_005255125.4:c.5670G=	XP_005255182.1:p.Gln1890=
XM_006720848.3:c.5826G=	XP_006720911.1:p.Gln1942=
XM_011522381.2:c.5334G=	XP_011520683.1:p.Gln1778=
XM_017022944.1:c.6081G=	XP_016878433.1:p.Gln2027=
NM_004380.3:c.6087G= MANE Select	NP_004371.2:p.Gln2029=