Canonical Allele Identifier: CA2202916287

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729204G= , CM000678.2:g.3729204G=	GRCh38
NC_000016.9:g.3779205G= , CM000678.1:g.3779205G=	GRCh37
NC_000016.8:g.3719206G=	NCBI36
NG_009873.1:g.155917C=
NG_009873.2:g.156510C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.5843C= MANE Select	ENSP00000262367.5:p.Pro1948=
ENST00000262367.9:c.5843C=	ENSP00000262367.5:p.Pro1948=
ENST00000382070.7:c.5729C=	ENSP00000371502.3:p.Pro1910=
NM_001079846.1:c.5729C=	NP_001073315.1:p.Pro1910=
NM_004380.2:c.5843C=	NP_004371.2:p.Pro1948=
XM_005255124.3:c.5798C=	XP_005255181.1:p.Pro1933=
XM_005255125.3:c.5426C=	XP_005255182.1:p.Pro1809=
XM_006720848.2:c.5582C=	XP_006720911.1:p.Pro1861=
XM_011522380.1:c.5789C=	XP_011520682.1:p.Pro1930=
XM_011522381.1:c.5090C=	XP_011520683.1:p.Pro1697=
XM_005255124.4:c.5798C=	XP_005255181.1:p.Pro1933=
XM_005255125.4:c.5426C=	XP_005255182.1:p.Pro1809=
XM_006720848.3:c.5582C=	XP_006720911.1:p.Pro1861=
XM_011522381.2:c.5090C=	XP_011520683.1:p.Pro1697=
XM_017022944.1:c.5837C=	XP_016878433.1:p.Pro1946=
NM_004380.3:c.5843C= MANE Select	NP_004371.2:p.Pro1948=