Canonical Allele Identifier: CA2202916495

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729695C= , CM000678.2:g.3729695C=	GRCh38
NC_000016.9:g.3779696C= , CM000678.1:g.3779696C=	GRCh37
NC_000016.8:g.3719697C=	NCBI36
NG_009873.1:g.155426G=
NG_009873.2:g.156019G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5352G= MANE Select	ENSP00000262367.5:p.Gln1784=
ENST00000262367.9:c.5352G=	ENSP00000262367.5:p.Gln1784=
ENST00000382070.7:c.5238G=	ENSP00000371502.3:p.Gln1746=
NM_001079846.1:c.5238G=	NP_001073315.1:p.Gln1746=
NM_004380.2:c.5352G=	NP_004371.2:p.Gln1784=
XM_005255124.3:c.5307G=	XP_005255181.1:p.Gln1769=
XM_005255125.3:c.4935G=	XP_005255182.1:p.Gln1645=
XM_006720848.2:c.5091G=	XP_006720911.1:p.Gln1697=
XM_011522380.1:c.5298G=	XP_011520682.1:p.Gln1766=
XM_011522381.1:c.4599G=	XP_011520683.1:p.Gln1533=
XM_005255124.4:c.5307G=	XP_005255181.1:p.Gln1769=
XM_005255125.4:c.4935G=	XP_005255182.1:p.Gln1645=
XM_006720848.3:c.5091G=	XP_006720911.1:p.Gln1697=
XM_011522381.2:c.4599G=	XP_011520683.1:p.Gln1533=
XM_017022944.1:c.5346G=	XP_016878433.1:p.Gln1782=
NM_004380.3:c.5352G= MANE Select	NP_004371.2:p.Gln1784=