Canonical Allele Identifier: CA2202971881

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3810774T= , CM000678.2:g.3810774T=	GRCh38
NC_000016.9:g.3860775T= , CM000678.1:g.3860775T=	GRCh37
NC_000016.8:g.3800776T=	NCBI36
NG_009873.1:g.74347A=
NG_009873.2:g.74940A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.804A= MANE Select	ENSP00000262367.5:p.Gly268=
ENST00000635899.1:n.46A=
ENST00000262367.9:c.804A=	ENSP00000262367.5:p.Gly268=
ENST00000382070.7:c.804A=	ENSP00000371502.3:p.Gly268=
NM_001079846.1:c.804A=	NP_001073315.1:p.Gly268=
NM_004380.2:c.804A=	NP_004371.2:p.Gly268=
XM_005255124.3:c.804A=	XP_005255181.1:p.Gly268=
XM_005255125.3:c.804A=	XP_005255182.1:p.Gly268=
XM_006720848.2:c.804A=	XP_006720911.1:p.Gly268=
XM_011522380.1:c.750A=	XP_011520682.1:p.Gly250=
XM_011522381.1:c.51A=	XP_011520683.1:p.Gly17=
XM_011522382.1:c.804A=	XP_011520684.1:p.Gly268=
XM_005255124.4:c.804A=	XP_005255181.1:p.Gly268=
XM_005255125.4:c.804A=	XP_005255182.1:p.Gly268=
XM_006720848.3:c.804A=	XP_006720911.1:p.Gly268=
XM_011522381.2:c.51A=	XP_011520683.1:p.Gly17=
XM_011522382.3:c.804A=	XP_011520684.1:p.Gly268=
XM_017022944.1:c.804A=	XP_016878433.1:p.Gly268=
NM_004380.3:c.804A= MANE Select	NP_004371.2:p.Gly268=