Canonical Allele Identifier: CA2202928405

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727922G= , CM000678.2:g.3727922G=	GRCh38
NC_000016.9:g.3777923G= , CM000678.1:g.3777923G=	GRCh37
NC_000016.8:g.3717924G=	NCBI36
NG_009873.1:g.157199C=
NG_009873.2:g.157792C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7125C= MANE Select	ENSP00000262367.5:p.His2375=
ENST00000262367.9:c.7125C=	ENSP00000262367.5:p.His2375=
ENST00000382070.7:c.7011C=	ENSP00000371502.3:p.His2337=
NM_001079846.1:c.7011C=	NP_001073315.1:p.His2337=
NM_004380.2:c.7125C=	NP_004371.2:p.His2375=
XM_005255124.3:c.7080C=	XP_005255181.1:p.His2360=
XM_005255125.3:c.6708C=	XP_005255182.1:p.His2236=
XM_006720848.2:c.6864C=	XP_006720911.1:p.His2288=
XM_011522380.1:c.7071C=	XP_011520682.1:p.His2357=
XM_011522381.1:c.6372C=	XP_011520683.1:p.His2124=
XM_005255124.4:c.7080C=	XP_005255181.1:p.His2360=
XM_005255125.4:c.6708C=	XP_005255182.1:p.His2236=
XM_006720848.3:c.6864C=	XP_006720911.1:p.His2288=
XM_011522381.2:c.6372C=	XP_011520683.1:p.His2124=
XM_017022944.1:c.7119C=	XP_016878433.1:p.His2373=
NM_004380.3:c.7125C= MANE Select	NP_004371.2:p.His2375=