Canonical Allele Identifier: CA2202928468

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728073G= , CM000678.2:g.3728073G=	GRCh38
NC_000016.9:g.3778074G= , CM000678.1:g.3778074G=	GRCh37
NC_000016.8:g.3718075G=	NCBI36
NG_009873.1:g.157048C=
NG_009873.2:g.157641C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6974C= MANE Select	ENSP00000262367.5:p.Pro2325=
ENST00000262367.9:c.6974C=	ENSP00000262367.5:p.Pro2325=
ENST00000382070.7:c.6860C=	ENSP00000371502.3:p.Pro2287=
NM_001079846.1:c.6860C=	NP_001073315.1:p.Pro2287=
NM_004380.2:c.6974C=	NP_004371.2:p.Pro2325=
XM_005255124.3:c.6929C=	XP_005255181.1:p.Pro2310=
XM_005255125.3:c.6557C=	XP_005255182.1:p.Pro2186=
XM_006720848.2:c.6713C=	XP_006720911.1:p.Pro2238=
XM_011522380.1:c.6920C=	XP_011520682.1:p.Pro2307=
XM_011522381.1:c.6221C=	XP_011520683.1:p.Pro2074=
XM_005255124.4:c.6929C=	XP_005255181.1:p.Pro2310=
XM_005255125.4:c.6557C=	XP_005255182.1:p.Pro2186=
XM_006720848.3:c.6713C=	XP_006720911.1:p.Pro2238=
XM_011522381.2:c.6221C=	XP_011520683.1:p.Pro2074=
XM_017022944.1:c.6968C=	XP_016878433.1:p.Pro2323=
NM_004380.3:c.6974C= MANE Select	NP_004371.2:p.Pro2325=