Canonical Allele Identifier: CA2202916475

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729641C= , CM000678.2:g.3729641C=	GRCh38
NC_000016.9:g.3779642C= , CM000678.1:g.3779642C=	GRCh37
NC_000016.8:g.3719643C=	NCBI36
NG_009873.1:g.155480G=
NG_009873.2:g.156073G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5406G= MANE Select	ENSP00000262367.5:p.Val1802=
ENST00000262367.9:c.5406G=	ENSP00000262367.5:p.Val1802=
ENST00000382070.7:c.5292G=	ENSP00000371502.3:p.Val1764=
NM_001079846.1:c.5292G=	NP_001073315.1:p.Val1764=
NM_004380.2:c.5406G=	NP_004371.2:p.Val1802=
XM_005255124.3:c.5361G=	XP_005255181.1:p.Val1787=
XM_005255125.3:c.4989G=	XP_005255182.1:p.Val1663=
XM_006720848.2:c.5145G=	XP_006720911.1:p.Val1715=
XM_011522380.1:c.5352G=	XP_011520682.1:p.Val1784=
XM_011522381.1:c.4653G=	XP_011520683.1:p.Val1551=
XM_005255124.4:c.5361G=	XP_005255181.1:p.Val1787=
XM_005255125.4:c.4989G=	XP_005255182.1:p.Val1663=
XM_006720848.3:c.5145G=	XP_006720911.1:p.Val1715=
XM_011522381.2:c.4653G=	XP_011520683.1:p.Val1551=
XM_017022944.1:c.5400G=	XP_016878433.1:p.Val1800=
NM_004380.3:c.5406G= MANE Select	NP_004371.2:p.Val1802=