Canonical Allele Identifier: CA2202928467

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728070T= , CM000678.2:g.3728070T=	GRCh38
NC_000016.9:g.3778071T= , CM000678.1:g.3778071T=	GRCh37
NC_000016.8:g.3718072T=	NCBI36
NG_009873.1:g.157051A=
NG_009873.2:g.157644A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6977A= MANE Select	ENSP00000262367.5:p.Gln2326=
ENST00000262367.9:c.6977A=	ENSP00000262367.5:p.Gln2326=
ENST00000382070.7:c.6863A=	ENSP00000371502.3:p.Gln2288=
NM_001079846.1:c.6863A=	NP_001073315.1:p.Gln2288=
NM_004380.2:c.6977A=	NP_004371.2:p.Gln2326=
XM_005255124.3:c.6932A=	XP_005255181.1:p.Gln2311=
XM_005255125.3:c.6560A=	XP_005255182.1:p.Gln2187=
XM_006720848.2:c.6716A=	XP_006720911.1:p.Gln2239=
XM_011522380.1:c.6923A=	XP_011520682.1:p.Gln2308=
XM_011522381.1:c.6224A=	XP_011520683.1:p.Gln2075=
XM_005255124.4:c.6932A=	XP_005255181.1:p.Gln2311=
XM_005255125.4:c.6560A=	XP_005255182.1:p.Gln2187=
XM_006720848.3:c.6716A=	XP_006720911.1:p.Gln2239=
XM_011522381.2:c.6224A=	XP_011520683.1:p.Gln2075=
XM_017022944.1:c.6971A=	XP_016878433.1:p.Gln2324=
NM_004380.3:c.6977A= MANE Select	NP_004371.2:p.Gln2326=