Canonical Allele Identifier: CA2202928275

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727671C= , CM000678.2:g.3727671C=	GRCh38
NC_000016.9:g.3777672C= , CM000678.1:g.3777672C=	GRCh37
NC_000016.8:g.3717673C=	NCBI36
NG_009873.1:g.157450G=
NG_009873.2:g.158043G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.*47G= MANE Select	ENSP00000262367.5:n.*47G=
ENST00000262367.9:c.*47G=	ENSP00000262367.5:n.*47G=
ENST00000382070.7:c.*47G=	ENSP00000371502.3:n.*47G=
NM_001079846.1:c.*47G=	NP_001073315.1:n.*47G=
NM_004380.2:c.*47G=	NP_004371.2:n.*47G=
XM_005255124.3:c.*47G=	XP_005255181.1:n.*47G=
XM_005255125.3:c.*47G=	XP_005255182.1:n.*47G=
XM_006720848.2:c.*47G=	XP_006720911.1:n.*47G=
XM_011522380.1:c.*47G=	XP_011520682.1:n.*47G=
XM_011522381.1:c.*47G=	XP_011520683.1:n.*47G=
XM_005255124.4:c.*47G=	XP_005255181.1:n.*47G=
XM_005255125.4:c.*47G=	XP_005255182.1:n.*47G=
XM_006720848.3:c.*47G=	XP_006720911.1:n.*47G=
XM_011522381.2:c.*47G=	XP_011520683.1:n.*47G=
XM_017022944.1:c.*47G=	XP_016878433.1:n.*47G=
NM_004380.3:c.*47G= MANE Select	NP_004371.2:n.*47G=