Canonical Allele Identifier: CA2202928445

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728019A= , CM000678.2:g.3728019A=	GRCh38
NC_000016.9:g.3778020A= , CM000678.1:g.3778020A=	GRCh37
NC_000016.8:g.3718021A=	NCBI36
NG_009873.1:g.157102T=
NG_009873.2:g.157695T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7028T= MANE Select	ENSP00000262367.5:p.Val2343=
ENST00000262367.9:c.7028T=	ENSP00000262367.5:p.Val2343=
ENST00000382070.7:c.6914T=	ENSP00000371502.3:p.Val2305=
NM_001079846.1:c.6914T=	NP_001073315.1:p.Val2305=
NM_004380.2:c.7028T=	NP_004371.2:p.Val2343=
XM_005255124.3:c.6983T=	XP_005255181.1:p.Val2328=
XM_005255125.3:c.6611T=	XP_005255182.1:p.Val2204=
XM_006720848.2:c.6767T=	XP_006720911.1:p.Val2256=
XM_011522380.1:c.6974T=	XP_011520682.1:p.Val2325=
XM_011522381.1:c.6275T=	XP_011520683.1:p.Val2092=
XM_005255124.4:c.6983T=	XP_005255181.1:p.Val2328=
XM_005255125.4:c.6611T=	XP_005255182.1:p.Val2204=
XM_006720848.3:c.6767T=	XP_006720911.1:p.Val2256=
XM_011522381.2:c.6275T=	XP_011520683.1:p.Val2092=
XM_017022944.1:c.7022T=	XP_016878433.1:p.Val2341=
NM_004380.3:c.7028T= MANE Select	NP_004371.2:p.Val2343=