Canonical Allele Identifier: CA2202916510

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729728C= , CM000678.2:g.3729728C=	GRCh38
NC_000016.9:g.3779729C= , CM000678.1:g.3779729C=	GRCh37
NC_000016.8:g.3719730C=	NCBI36
NG_009873.1:g.155393G=
NG_009873.2:g.155986G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5319G= MANE Select	ENSP00000262367.5:p.Gln1773=
ENST00000262367.9:c.5319G=	ENSP00000262367.5:p.Gln1773=
ENST00000382070.7:c.5205G=	ENSP00000371502.3:p.Gln1735=
NM_001079846.1:c.5205G=	NP_001073315.1:p.Gln1735=
NM_004380.2:c.5319G=	NP_004371.2:p.Gln1773=
XM_005255124.3:c.5274G=	XP_005255181.1:p.Gln1758=
XM_005255125.3:c.4902G=	XP_005255182.1:p.Gln1634=
XM_006720848.2:c.5058G=	XP_006720911.1:p.Gln1686=
XM_011522380.1:c.5265G=	XP_011520682.1:p.Gln1755=
XM_011522381.1:c.4566G=	XP_011520683.1:p.Gln1522=
XM_005255124.4:c.5274G=	XP_005255181.1:p.Gln1758=
XM_005255125.4:c.4902G=	XP_005255182.1:p.Gln1634=
XM_006720848.3:c.5058G=	XP_006720911.1:p.Gln1686=
XM_011522381.2:c.4566G=	XP_011520683.1:p.Gln1522=
XM_017022944.1:c.5313G=	XP_016878433.1:p.Gln1771=
NM_004380.3:c.5319G= MANE Select	NP_004371.2:p.Gln1773=