Canonical Allele Identifier: CA2202928380

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727876T= , CM000678.2:g.3727876T=	GRCh38
NC_000016.9:g.3777877T= , CM000678.1:g.3777877T=	GRCh37
NC_000016.8:g.3717878T=	NCBI36
NG_009873.1:g.157245A=
NG_009873.2:g.157838A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7171A= MANE Select	ENSP00000262367.5:p.Met2391=
ENST00000262367.9:c.7171A=	ENSP00000262367.5:p.Met2391=
ENST00000382070.7:c.7057A=	ENSP00000371502.3:p.Met2353=
NM_001079846.1:c.7057A=	NP_001073315.1:p.Met2353=
NM_004380.2:c.7171A=	NP_004371.2:p.Met2391=
XM_005255124.3:c.7126A=	XP_005255181.1:p.Met2376=
XM_005255125.3:c.6754A=	XP_005255182.1:p.Met2252=
XM_006720848.2:c.6910A=	XP_006720911.1:p.Met2304=
XM_011522380.1:c.7117A=	XP_011520682.1:p.Met2373=
XM_011522381.1:c.6418A=	XP_011520683.1:p.Met2140=
XM_005255124.4:c.7126A=	XP_005255181.1:p.Met2376=
XM_005255125.4:c.6754A=	XP_005255182.1:p.Met2252=
XM_006720848.3:c.6910A=	XP_006720911.1:p.Met2304=
XM_011522381.2:c.6418A=	XP_011520683.1:p.Met2140=
XM_017022944.1:c.7165A=	XP_016878433.1:p.Met2389=
NM_004380.3:c.7171A= MANE Select	NP_004371.2:p.Met2391=