Canonical Allele Identifier: CA2202939044

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3738683G= , CM000678.2:g.3738683G=	GRCh38
NC_000016.9:g.3788684G= , CM000678.1:g.3788684G=	GRCh37
NC_000016.8:g.3728685G=	NCBI36
NG_009873.1:g.146438C=
NG_009873.2:g.147031C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4281-11C= MANE Select	ENSP00000262367.5:n.4281-11C=
ENST00000262367.9:c.4281-11C=	ENSP00000262367.5:n.4281-11C=
ENST00000382070.7:c.4167-11C=	ENSP00000371502.3:n.4167-11C=
ENST00000570939.2:c.2916-11C=	ENSP00000461002.2:n.2916-11C=
ENST00000574740.1:n.215+1716C=
ENST00000576720.1:n.3217+895C=
NM_001079846.1:c.4167-11C=	NP_001073315.1:n.4167-11C=
NM_004380.2:c.4281-11C=	NP_004371.2:n.4281-11C=
XM_005255124.3:c.4236-11C=	XP_005255181.1:n.4236-11C=
XM_005255125.3:c.3864-11C=	XP_005255182.1:n.3864-11C=
XM_006720848.2:c.4133+1716C=	XP_006720911.1:n.4133+1716C=
XM_011522380.1:c.4227-11C=	XP_011520682.1:n.4227-11C=
XM_011522381.1:c.3528-11C=	XP_011520683.1:n.3528-11C=
XM_005255124.4:c.4236-11C=	XP_005255181.1:n.4236-11C=
XM_005255125.4:c.3864-11C=	XP_005255182.1:n.3864-11C=
XM_006720848.3:c.4133+1716C=	XP_006720911.1:n.4133+1716C=
XM_011522381.2:c.3528-11C=	XP_011520683.1:n.3528-11C=
XM_017022944.1:c.4275-11C=	XP_016878433.1:n.4275-11C=
NM_004380.3:c.4281-11C= MANE Select	NP_004371.2:n.4281-11C=