Canonical Allele Identifier: CA2202928432

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727984G= , CM000678.2:g.3727984G=	GRCh38
NC_000016.9:g.3777985G= , CM000678.1:g.3777985G=	GRCh37
NC_000016.8:g.3717986G=	NCBI36
NG_009873.1:g.157137C=
NG_009873.2:g.157730C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7063C= MANE Select	ENSP00000262367.5:p.Gln2355=
ENST00000262367.9:c.7063C=	ENSP00000262367.5:p.Gln2355=
ENST00000382070.7:c.6949C=	ENSP00000371502.3:p.Gln2317=
NM_001079846.1:c.6949C=	NP_001073315.1:p.Gln2317=
NM_004380.2:c.7063C=	NP_004371.2:p.Gln2355=
XM_005255124.3:c.7018C=	XP_005255181.1:p.Gln2340=
XM_005255125.3:c.6646C=	XP_005255182.1:p.Gln2216=
XM_006720848.2:c.6802C=	XP_006720911.1:p.Gln2268=
XM_011522380.1:c.7009C=	XP_011520682.1:p.Gln2337=
XM_011522381.1:c.6310C=	XP_011520683.1:p.Gln2104=
XM_005255124.4:c.7018C=	XP_005255181.1:p.Gln2340=
XM_005255125.4:c.6646C=	XP_005255182.1:p.Gln2216=
XM_006720848.3:c.6802C=	XP_006720911.1:p.Gln2268=
XM_011522381.2:c.6310C=	XP_011520683.1:p.Gln2104=
XM_017022944.1:c.7057C=	XP_016878433.1:p.Gln2353=
NM_004380.3:c.7063C= MANE Select	NP_004371.2:p.Gln2355=