Canonical Allele Identifier: CA2202928891

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728879C= , CM000678.2:g.3728879C=	GRCh38
NC_000016.9:g.3778880C= , CM000678.1:g.3778880C=	GRCh37
NC_000016.8:g.3718881C=	NCBI36
NG_009873.1:g.156242G=
NG_009873.2:g.156835G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6168G= MANE Select	ENSP00000262367.5:p.Val2056=
ENST00000262367.9:c.6168G=	ENSP00000262367.5:p.Val2056=
ENST00000382070.7:c.6054G=	ENSP00000371502.3:p.Val2018=
NM_001079846.1:c.6054G=	NP_001073315.1:p.Val2018=
NM_004380.2:c.6168G=	NP_004371.2:p.Val2056=
XM_005255124.3:c.6123G=	XP_005255181.1:p.Val2041=
XM_005255125.3:c.5751G=	XP_005255182.1:p.Val1917=
XM_006720848.2:c.5907G=	XP_006720911.1:p.Val1969=
XM_011522380.1:c.6114G=	XP_011520682.1:p.Val2038=
XM_011522381.1:c.5415G=	XP_011520683.1:p.Val1805=
XM_005255124.4:c.6123G=	XP_005255181.1:p.Val2041=
XM_005255125.4:c.5751G=	XP_005255182.1:p.Val1917=
XM_006720848.3:c.5907G=	XP_006720911.1:p.Val1969=
XM_011522381.2:c.5415G=	XP_011520683.1:p.Val1805=
XM_017022944.1:c.6162G=	XP_016878433.1:p.Val2054=
NM_004380.3:c.6168G= MANE Select	NP_004371.2:p.Val2056=