Canonical Allele Identifier: CA2202916160

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729012A= , CM000678.2:g.3729012A=	GRCh38
NC_000016.9:g.3779013A= , CM000678.1:g.3779013A=	GRCh37
NC_000016.8:g.3719014A=	NCBI36
NG_009873.1:g.156109T=
NG_009873.2:g.156702T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6035T= MANE Select	ENSP00000262367.5:p.Val2012=
ENST00000262367.9:c.6035T=	ENSP00000262367.5:p.Val2012=
ENST00000382070.7:c.5921T=	ENSP00000371502.3:p.Val1974=
NM_001079846.1:c.5921T=	NP_001073315.1:p.Val1974=
NM_004380.2:c.6035T=	NP_004371.2:p.Val2012=
XM_005255124.3:c.5990T=	XP_005255181.1:p.Val1997=
XM_005255125.3:c.5618T=	XP_005255182.1:p.Val1873=
XM_006720848.2:c.5774T=	XP_006720911.1:p.Val1925=
XM_011522380.1:c.5981T=	XP_011520682.1:p.Val1994=
XM_011522381.1:c.5282T=	XP_011520683.1:p.Val1761=
XM_005255124.4:c.5990T=	XP_005255181.1:p.Val1997=
XM_005255125.4:c.5618T=	XP_005255182.1:p.Val1873=
XM_006720848.3:c.5774T=	XP_006720911.1:p.Val1925=
XM_011522381.2:c.5282T=	XP_011520683.1:p.Val1761=
XM_017022944.1:c.6029T=	XP_016878433.1:p.Val2010=
NM_004380.3:c.6035T= MANE Select	NP_004371.2:p.Val2012=