Canonical Allele Identifier: CA2202916509

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729724A= , CM000678.2:g.3729724A=	GRCh38
NC_000016.9:g.3779725A= , CM000678.1:g.3779725A=	GRCh37
NC_000016.8:g.3719726A=	NCBI36
NG_009873.1:g.155397T=
NG_009873.2:g.155990T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5323T= MANE Select	ENSP00000262367.5:p.Cys1775=
ENST00000262367.9:c.5323T=	ENSP00000262367.5:p.Cys1775=
ENST00000382070.7:c.5209T=	ENSP00000371502.3:p.Cys1737=
NM_001079846.1:c.5209T=	NP_001073315.1:p.Cys1737=
NM_004380.2:c.5323T=	NP_004371.2:p.Cys1775=
XM_005255124.3:c.5278T=	XP_005255181.1:p.Cys1760=
XM_005255125.3:c.4906T=	XP_005255182.1:p.Cys1636=
XM_006720848.2:c.5062T=	XP_006720911.1:p.Cys1688=
XM_011522380.1:c.5269T=	XP_011520682.1:p.Cys1757=
XM_011522381.1:c.4570T=	XP_011520683.1:p.Cys1524=
XM_005255124.4:c.5278T=	XP_005255181.1:p.Cys1760=
XM_005255125.4:c.4906T=	XP_005255182.1:p.Cys1636=
XM_006720848.3:c.5062T=	XP_006720911.1:p.Cys1688=
XM_011522381.2:c.4570T=	XP_011520683.1:p.Cys1524=
XM_017022944.1:c.5317T=	XP_016878433.1:p.Cys1773=
NM_004380.3:c.5323T= MANE Select	NP_004371.2:p.Cys1775=