Canonical Allele Identifier: CA2202916252

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729148G= , CM000678.2:g.3729148G=	GRCh38
NC_000016.9:g.3779149G= , CM000678.1:g.3779149G=	GRCh37
NC_000016.8:g.3719150G=	NCBI36
NG_009873.1:g.155973C=
NG_009873.2:g.156566C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5899C= MANE Select	ENSP00000262367.5:p.Gln1967=
ENST00000262367.9:c.5899C=	ENSP00000262367.5:p.Gln1967=
ENST00000382070.7:c.5785C=	ENSP00000371502.3:p.Gln1929=
NM_001079846.1:c.5785C=	NP_001073315.1:p.Gln1929=
NM_004380.2:c.5899C=	NP_004371.2:p.Gln1967=
XM_005255124.3:c.5854C=	XP_005255181.1:p.Gln1952=
XM_005255125.3:c.5482C=	XP_005255182.1:p.Gln1828=
XM_006720848.2:c.5638C=	XP_006720911.1:p.Gln1880=
XM_011522380.1:c.5845C=	XP_011520682.1:p.Gln1949=
XM_011522381.1:c.5146C=	XP_011520683.1:p.Gln1716=
XM_005255124.4:c.5854C=	XP_005255181.1:p.Gln1952=
XM_005255125.4:c.5482C=	XP_005255182.1:p.Gln1828=
XM_006720848.3:c.5638C=	XP_006720911.1:p.Gln1880=
XM_011522381.2:c.5146C=	XP_011520683.1:p.Gln1716=
XM_017022944.1:c.5893C=	XP_016878433.1:p.Gln1965=
NM_004380.3:c.5899C= MANE Select	NP_004371.2:p.Gln1967=