Canonical Allele Identifier: CA2202928277

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727674A= , CM000678.2:g.3727674A=	GRCh38
NC_000016.9:g.3777675A= , CM000678.1:g.3777675A=	GRCh37
NC_000016.8:g.3717676A=	NCBI36
NG_009873.1:g.157447T=
NG_009873.2:g.158040T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.*44T= MANE Select	ENSP00000262367.5:n.*44T=
ENST00000262367.9:c.*44T=	ENSP00000262367.5:n.*44T=
ENST00000382070.7:c.*44T=	ENSP00000371502.3:n.*44T=
NM_001079846.1:c.*44T=	NP_001073315.1:n.*44T=
NM_004380.2:c.*44T=	NP_004371.2:n.*44T=
XM_005255124.3:c.*44T=	XP_005255181.1:n.*44T=
XM_005255125.3:c.*44T=	XP_005255182.1:n.*44T=
XM_006720848.2:c.*44T=	XP_006720911.1:n.*44T=
XM_011522380.1:c.*44T=	XP_011520682.1:n.*44T=
XM_011522381.1:c.*44T=	XP_011520683.1:n.*44T=
XM_005255124.4:c.*44T=	XP_005255181.1:n.*44T=
XM_005255125.4:c.*44T=	XP_005255182.1:n.*44T=
XM_006720848.3:c.*44T=	XP_006720911.1:n.*44T=
XM_011522381.2:c.*44T=	XP_011520683.1:n.*44T=
XM_017022944.1:c.*44T=	XP_016878433.1:n.*44T=
NM_004380.3:c.*44T= MANE Select	NP_004371.2:n.*44T=