Canonical Allele Identifier: CA2202928791

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728650T= , CM000678.2:g.3728650T=	GRCh38
NC_000016.9:g.3778651T= , CM000678.1:g.3778651T=	GRCh37
NC_000016.8:g.3718652T=	NCBI36
NG_009873.1:g.156471A=
NG_009873.2:g.157064A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6397A= MANE Select	ENSP00000262367.5:p.Met2133=
ENST00000262367.9:c.6397A=	ENSP00000262367.5:p.Met2133=
ENST00000382070.7:c.6283A=	ENSP00000371502.3:p.Met2095=
NM_001079846.1:c.6283A=	NP_001073315.1:p.Met2095=
NM_004380.2:c.6397A=	NP_004371.2:p.Met2133=
XM_005255124.3:c.6352A=	XP_005255181.1:p.Met2118=
XM_005255125.3:c.5980A=	XP_005255182.1:p.Met1994=
XM_006720848.2:c.6136A=	XP_006720911.1:p.Met2046=
XM_011522380.1:c.6343A=	XP_011520682.1:p.Met2115=
XM_011522381.1:c.5644A=	XP_011520683.1:p.Met1882=
XM_005255124.4:c.6352A=	XP_005255181.1:p.Met2118=
XM_005255125.4:c.5980A=	XP_005255182.1:p.Met1994=
XM_006720848.3:c.6136A=	XP_006720911.1:p.Met2046=
XM_011522381.2:c.5644A=	XP_011520683.1:p.Met1882=
XM_017022944.1:c.6391A=	XP_016878433.1:p.Met2131=
NM_004380.3:c.6397A= MANE Select	NP_004371.2:p.Met2133=