Canonical Allele Identifier: CA2202958710

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3778054A= , CM000678.2:g.3778054A=	GRCh38
NC_000016.9:g.3828055A= , CM000678.1:g.3828055A=	GRCh37
NC_000016.8:g.3768056A=	NCBI36
NG_009873.1:g.107067T=
NG_009873.2:g.107660T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2070T= MANE Select	ENSP00000262367.5:p.Ala690=
ENST00000262367.9:c.2070T=	ENSP00000262367.5:p.Ala690=
ENST00000382070.7:c.1956T=	ENSP00000371502.3:p.Ala652=
ENST00000570939.2:c.675T=	ENSP00000461002.2:p.Ala225=
ENST00000571826.5:c.119T=
ENST00000572134.1:c.383T=
ENST00000634839.1:n.232T=
NM_001079846.1:c.1956T=	NP_001073315.1:p.Ala652=
NM_004380.2:c.2070T=	NP_004371.2:p.Ala690=
XM_005255124.3:c.2070T=	XP_005255181.1:p.Ala690=
XM_005255125.3:c.2070T=	XP_005255182.1:p.Ala690=
XM_006720848.2:c.2070T=	XP_006720911.1:p.Ala690=
XM_011522380.1:c.2016T=	XP_011520682.1:p.Ala672=
XM_011522381.1:c.1317T=	XP_011520683.1:p.Ala439=
XM_011522382.1:c.2070T=	XP_011520684.1:p.Ala690=
XM_005255124.4:c.2070T=	XP_005255181.1:p.Ala690=
XM_005255125.4:c.2070T=	XP_005255182.1:p.Ala690=
XM_006720848.3:c.2070T=	XP_006720911.1:p.Ala690=
XM_011522381.2:c.1317T=	XP_011520683.1:p.Ala439=
XM_011522382.3:c.2070T=	XP_011520684.1:p.Ala690=
XM_017022944.1:c.2070T=	XP_016878433.1:p.Ala690=
NM_004380.3:c.2070T= MANE Select	NP_004371.2:p.Ala690=