Canonical Allele Identifier: CA2202916456

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729577C= , CM000678.2:g.3729577C=	GRCh38
NC_000016.9:g.3779578C= , CM000678.1:g.3779578C=	GRCh37
NC_000016.8:g.3719579C=	NCBI36
NG_009873.1:g.155544G=
NG_009873.2:g.156137G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5470G= MANE Select	ENSP00000262367.5:p.Ala1824=
ENST00000262367.9:c.5470G=	ENSP00000262367.5:p.Ala1824=
ENST00000382070.7:c.5356G=	ENSP00000371502.3:p.Ala1786=
NM_001079846.1:c.5356G=	NP_001073315.1:p.Ala1786=
NM_004380.2:c.5470G=	NP_004371.2:p.Ala1824=
XM_005255124.3:c.5425G=	XP_005255181.1:p.Ala1809=
XM_005255125.3:c.5053G=	XP_005255182.1:p.Ala1685=
XM_006720848.2:c.5209G=	XP_006720911.1:p.Ala1737=
XM_011522380.1:c.5416G=	XP_011520682.1:p.Ala1806=
XM_011522381.1:c.4717G=	XP_011520683.1:p.Ala1573=
XM_005255124.4:c.5425G=	XP_005255181.1:p.Ala1809=
XM_005255125.4:c.5053G=	XP_005255182.1:p.Ala1685=
XM_006720848.3:c.5209G=	XP_006720911.1:p.Ala1737=
XM_011522381.2:c.4717G=	XP_011520683.1:p.Ala1573=
XM_017022944.1:c.5464G=	XP_016878433.1:p.Ala1822=
NM_004380.3:c.5470G= MANE Select	NP_004371.2:p.Ala1824=