Canonical Allele Identifier: CA2202994261

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3850914G= , CM000678.2:g.3850914G=	GRCh38
NC_000016.9:g.3900915G= , CM000678.1:g.3900915G=	GRCh37
NC_000016.8:g.3840916G=	NCBI36
NG_009873.1:g.34207C=
NG_009873.2:g.34800C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.181C= MANE Select	ENSP00000262367.5:p.Pro61=
ENST00000262367.9:c.181C=	ENSP00000262367.5:p.Pro61=
ENST00000382070.7:c.181C=	ENSP00000371502.3:p.Pro61=
NM_001079846.1:c.181C=	NP_001073315.1:p.Pro61=
NM_004380.2:c.181C=	NP_004371.2:p.Pro61=
XM_005255124.3:c.181C=	XP_005255181.1:p.Pro61=
XM_005255125.3:c.181C=	XP_005255182.1:p.Pro61=
XM_006720848.2:c.181C=	XP_006720911.1:p.Pro61=
XM_011522380.1:c.127C=	XP_011520682.1:p.Pro43=
XM_011522382.1:c.181C=	XP_011520684.1:p.Pro61=
XM_005255124.4:c.181C=	XP_005255181.1:p.Pro61=
XM_005255125.4:c.181C=	XP_005255182.1:p.Pro61=
XM_006720848.3:c.181C=	XP_006720911.1:p.Pro61=
XM_011522382.3:c.181C=	XP_011520684.1:p.Pro61=
XM_017022944.1:c.181C=	XP_016878433.1:p.Pro61=
NM_004380.3:c.181C= MANE Select	NP_004371.2:p.Pro61=