Canonical Allele Identifier: CA2202916168

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729020G= , CM000678.2:g.3729020G=	GRCh38
NC_000016.9:g.3779021G= , CM000678.1:g.3779021G=	GRCh37
NC_000016.8:g.3719022G=	NCBI36
NG_009873.1:g.156101C=
NG_009873.2:g.156694C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.6027C= MANE Select	ENSP00000262367.5:p.Ser2009=
ENST00000262367.9:c.6027C=	ENSP00000262367.5:p.Ser2009=
ENST00000382070.7:c.5913C=	ENSP00000371502.3:p.Ser1971=
NM_001079846.1:c.5913C=	NP_001073315.1:p.Ser1971=
NM_004380.2:c.6027C=	NP_004371.2:p.Ser2009=
XM_005255124.3:c.5982C=	XP_005255181.1:p.Ser1994=
XM_005255125.3:c.5610C=	XP_005255182.1:p.Ser1870=
XM_006720848.2:c.5766C=	XP_006720911.1:p.Ser1922=
XM_011522380.1:c.5973C=	XP_011520682.1:p.Ser1991=
XM_011522381.1:c.5274C=	XP_011520683.1:p.Ser1758=
XM_005255124.4:c.5982C=	XP_005255181.1:p.Ser1994=
XM_005255125.4:c.5610C=	XP_005255182.1:p.Ser1870=
XM_006720848.3:c.5766C=	XP_006720911.1:p.Ser1922=
XM_011522381.2:c.5274C=	XP_011520683.1:p.Ser1758=
XM_017022944.1:c.6021C=	XP_016878433.1:p.Ser2007=
NM_004380.3:c.6027C= MANE Select	NP_004371.2:p.Ser2009=