Canonical Allele Identifier: CA2202928845

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728765C= , CM000678.2:g.3728765C=	GRCh38
NC_000016.9:g.3778766C= , CM000678.1:g.3778766C=	GRCh37
NC_000016.8:g.3718767C=	NCBI36
NG_009873.1:g.156356G=
NG_009873.2:g.156949G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6282G= MANE Select	ENSP00000262367.5:p.Pro2094=
ENST00000262367.9:c.6282G=	ENSP00000262367.5:p.Pro2094=
ENST00000382070.7:c.6168G=	ENSP00000371502.3:p.Pro2056=
NM_001079846.1:c.6168G=	NP_001073315.1:p.Pro2056=
NM_004380.2:c.6282G=	NP_004371.2:p.Pro2094=
XM_005255124.3:c.6237G=	XP_005255181.1:p.Pro2079=
XM_005255125.3:c.5865G=	XP_005255182.1:p.Pro1955=
XM_006720848.2:c.6021G=	XP_006720911.1:p.Pro2007=
XM_011522380.1:c.6228G=	XP_011520682.1:p.Pro2076=
XM_011522381.1:c.5529G=	XP_011520683.1:p.Pro1843=
XM_005255124.4:c.6237G=	XP_005255181.1:p.Pro2079=
XM_005255125.4:c.5865G=	XP_005255182.1:p.Pro1955=
XM_006720848.3:c.6021G=	XP_006720911.1:p.Pro2007=
XM_011522381.2:c.5529G=	XP_011520683.1:p.Pro1843=
XM_017022944.1:c.6276G=	XP_016878433.1:p.Pro2092=
NM_004380.3:c.6282G= MANE Select	NP_004371.2:p.Pro2094=