Canonical Allele Identifier: CA2202958062

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3777544A= , CM000678.2:g.3777544A=	GRCh38
NC_000016.9:g.3827545A= , CM000678.1:g.3827545A=	GRCh37
NC_000016.8:g.3767546A=	NCBI36
NG_009873.1:g.107577T=
NG_009873.2:g.108170T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2158+69T= MANE Select	ENSP00000262367.5:n.2158+69T=
ENST00000262367.9:c.2158+69T=	ENSP00000262367.5:n.2158+69T=
ENST00000382070.7:c.2044+69T=	ENSP00000371502.3:n.2044+69T=
ENST00000570939.2:c.763+69T=	ENSP00000461002.2:n.763+69T=
ENST00000571826.5:c.207+69T=
ENST00000572134.1:c.426+467T=
NM_001079846.1:c.2044+69T=	NP_001073315.1:n.2044+69T=
NM_004380.2:c.2158+69T=	NP_004371.2:n.2158+69T=
XM_005255124.3:c.2113+467T=	XP_005255181.1:n.2113+467T=
XM_005255125.3:c.2158+69T=	XP_005255182.1:n.2158+69T=
XM_006720848.2:c.2158+69T=	XP_006720911.1:n.2158+69T=
XM_011522380.1:c.2104+69T=	XP_011520682.1:n.2104+69T=
XM_011522381.1:c.1405+69T=	XP_011520683.1:n.1405+69T=
XM_011522382.1:c.2158+69T=	XP_011520684.1:n.2158+69T=
XM_005255124.4:c.2113+467T=	XP_005255181.1:n.2113+467T=
XM_005255125.4:c.2158+69T=	XP_005255182.1:n.2158+69T=
XM_006720848.3:c.2158+69T=	XP_006720911.1:n.2158+69T=
XM_011522381.2:c.1405+69T=	XP_011520683.1:n.1405+69T=
XM_011522382.3:c.2158+69T=	XP_011520684.1:n.2158+69T=
XM_017022944.1:c.2158+69T=	XP_016878433.1:n.2158+69T=
NM_004380.3:c.2158+69T= MANE Select	NP_004371.2:n.2158+69T=