Canonical Allele Identifier: CA2202928327

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727766G= , CM000678.2:g.3727766G=	GRCh38
NC_000016.9:g.3777767G= , CM000678.1:g.3777767G=	GRCh37
NC_000016.8:g.3717768G=	NCBI36
NG_009873.1:g.157355C=
NG_009873.2:g.157948C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7281C= MANE Select	ENSP00000262367.5:p.Val2427=
ENST00000262367.9:c.7281C=	ENSP00000262367.5:p.Val2427=
ENST00000382070.7:c.7167C=	ENSP00000371502.3:p.Val2389=
NM_001079846.1:c.7167C=	NP_001073315.1:p.Val2389=
NM_004380.2:c.7281C=	NP_004371.2:p.Val2427=
XM_005255124.3:c.7236C=	XP_005255181.1:p.Val2412=
XM_005255125.3:c.6864C=	XP_005255182.1:p.Val2288=
XM_006720848.2:c.7020C=	XP_006720911.1:p.Val2340=
XM_011522380.1:c.7227C=	XP_011520682.1:p.Val2409=
XM_011522381.1:c.6528C=	XP_011520683.1:p.Val2176=
XM_005255124.4:c.7236C=	XP_005255181.1:p.Val2412=
XM_005255125.4:c.6864C=	XP_005255182.1:p.Val2288=
XM_006720848.3:c.7020C=	XP_006720911.1:p.Val2340=
XM_011522381.2:c.6528C=	XP_011520683.1:p.Val2176=
XM_017022944.1:c.7275C=	XP_016878433.1:p.Val2425=
NM_004380.3:c.7281C= MANE Select	NP_004371.2:p.Val2427=