Canonical Allele Identifier: CA2202936721

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736801T= , CM000678.2:g.3736801T=	GRCh38
NC_000016.9:g.3786802T= , CM000678.1:g.3786802T=	GRCh37
NC_000016.8:g.3726803T=	NCBI36
NG_009873.1:g.148320A=
NG_009873.2:g.148913A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4409A= MANE Select	ENSP00000262367.5:p.His1470=
ENST00000262367.9:c.4409A=	ENSP00000262367.5:p.His1470=
ENST00000382070.7:c.4295A=	ENSP00000371502.3:p.His1432=
ENST00000570939.2:c.3044A=	ENSP00000461002.2:p.His1015=
ENST00000571763.5:n.199A=
ENST00000574740.1:n.230A=
ENST00000576720.1:n.3232A=
NM_001079846.1:c.4295A=	NP_001073315.1:p.His1432=
NM_004380.2:c.4409A=	NP_004371.2:p.His1470=
XM_005255124.3:c.4364A=	XP_005255181.1:p.His1455=
XM_005255125.3:c.3992A=	XP_005255182.1:p.His1331=
XM_006720848.2:c.4148A=	XP_006720911.1:p.His1383=
XM_011522380.1:c.4355A=	XP_011520682.1:p.His1452=
XM_011522381.1:c.3656A=	XP_011520683.1:p.His1219=
XM_005255124.4:c.4364A=	XP_005255181.1:p.His1455=
XM_005255125.4:c.3992A=	XP_005255182.1:p.His1331=
XM_006720848.3:c.4148A=	XP_006720911.1:p.His1383=
XM_011522381.2:c.3656A=	XP_011520683.1:p.His1219=
XM_017022944.1:c.4403A=	XP_016878433.1:p.His1468=
NM_004380.3:c.4409A= MANE Select	NP_004371.2:p.His1470=