Canonical Allele Identifier: CA2202936573

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736681G= , CM000678.2:g.3736681G=	GRCh38
NC_000016.9:g.3786682G= , CM000678.1:g.3786682G=	GRCh37
NC_000016.8:g.3726683G=	NCBI36
NG_009873.1:g.148440C=
NG_009873.2:g.149033C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4529C= MANE Select	ENSP00000262367.5:p.Ala1510=
ENST00000262367.9:c.4529C=	ENSP00000262367.5:p.Ala1510=
ENST00000382070.7:c.4415C=	ENSP00000371502.3:p.Ala1472=
ENST00000570939.2:c.3164C=	ENSP00000461002.2:p.Ala1055=
ENST00000571763.5:n.319C=
ENST00000574740.1:n.350C=
ENST00000576720.1:n.3352C=
NM_001079846.1:c.4415C=	NP_001073315.1:p.Ala1472=
NM_004380.2:c.4529C=	NP_004371.2:p.Ala1510=
XM_005255124.3:c.4484C=	XP_005255181.1:p.Ala1495=
XM_005255125.3:c.4112C=	XP_005255182.1:p.Ala1371=
XM_006720848.2:c.4268C=	XP_006720911.1:p.Ala1423=
XM_011522380.1:c.4475C=	XP_011520682.1:p.Ala1492=
XM_011522381.1:c.3776C=	XP_011520683.1:p.Ala1259=
XM_005255124.4:c.4484C=	XP_005255181.1:p.Ala1495=
XM_005255125.4:c.4112C=	XP_005255182.1:p.Ala1371=
XM_006720848.3:c.4268C=	XP_006720911.1:p.Ala1423=
XM_011522381.2:c.3776C=	XP_011520683.1:p.Ala1259=
XM_017022944.1:c.4523C=	XP_016878433.1:p.Ala1508=
NM_004380.3:c.4529C= MANE Select	NP_004371.2:p.Ala1510=