Canonical Allele Identifier: CA2202928368

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727850G= , CM000678.2:g.3727850G=	GRCh38
NC_000016.9:g.3777851G= , CM000678.1:g.3777851G=	GRCh37
NC_000016.8:g.3717852G=	NCBI36
NG_009873.1:g.157271C=
NG_009873.2:g.157864C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7197C= MANE Select	ENSP00000262367.5:p.His2399=
ENST00000262367.9:c.7197C=	ENSP00000262367.5:p.His2399=
ENST00000382070.7:c.7083C=	ENSP00000371502.3:p.His2361=
NM_001079846.1:c.7083C=	NP_001073315.1:p.His2361=
NM_004380.2:c.7197C=	NP_004371.2:p.His2399=
XM_005255124.3:c.7152C=	XP_005255181.1:p.His2384=
XM_005255125.3:c.6780C=	XP_005255182.1:p.His2260=
XM_006720848.2:c.6936C=	XP_006720911.1:p.His2312=
XM_011522380.1:c.7143C=	XP_011520682.1:p.His2381=
XM_011522381.1:c.6444C=	XP_011520683.1:p.His2148=
XM_005255124.4:c.7152C=	XP_005255181.1:p.His2384=
XM_005255125.4:c.6780C=	XP_005255182.1:p.His2260=
XM_006720848.3:c.6936C=	XP_006720911.1:p.His2312=
XM_011522381.2:c.6444C=	XP_011520683.1:p.His2148=
XM_017022944.1:c.7191C=	XP_016878433.1:p.His2397=
NM_004380.3:c.7197C= MANE Select	NP_004371.2:p.His2399=