Canonical Allele Identifier: CA2202993965

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3850320C= , CM000678.2:g.3850320C=	GRCh38
NC_000016.9:g.3900321C= , CM000678.1:g.3900321C=	GRCh37
NC_000016.8:g.3840322C=	NCBI36
NG_009873.1:g.34801G=
NG_009873.2:g.35394G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.775G= MANE Select	ENSP00000262367.5:p.Ala259=
ENST00000636895.1:n.2G=
ENST00000262367.9:c.775G=	ENSP00000262367.5:p.Ala259=
ENST00000382070.7:c.775G=	ENSP00000371502.3:p.Ala259=
NM_001079846.1:c.775G=	NP_001073315.1:p.Ala259=
NM_004380.2:c.775G=	NP_004371.2:p.Ala259=
XM_005255124.3:c.775G=	XP_005255181.1:p.Ala259=
XM_005255125.3:c.775G=	XP_005255182.1:p.Ala259=
XM_006720848.2:c.775G=	XP_006720911.1:p.Ala259=
XM_011522380.1:c.721G=	XP_011520682.1:p.Ala241=
XM_011522382.1:c.775G=	XP_011520684.1:p.Ala259=
XM_005255124.4:c.775G=	XP_005255181.1:p.Ala259=
XM_005255125.4:c.775G=	XP_005255182.1:p.Ala259=
XM_006720848.3:c.775G=	XP_006720911.1:p.Ala259=
XM_011522382.3:c.775G=	XP_011520684.1:p.Ala259=
XM_017022944.1:c.775G=	XP_016878433.1:p.Ala259=
NM_004380.3:c.775G= MANE Select	NP_004371.2:p.Ala259=