Canonical Allele Identifier: CA2202916462

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729596C= , CM000678.2:g.3729596C=	GRCh38
NC_000016.9:g.3779597C= , CM000678.1:g.3779597C=	GRCh37
NC_000016.8:g.3719598C=	NCBI36
NG_009873.1:g.155525G=
NG_009873.2:g.156118G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5451G= MANE Select	ENSP00000262367.5:p.Pro1817=
ENST00000262367.9:c.5451G=	ENSP00000262367.5:p.Pro1817=
ENST00000382070.7:c.5337G=	ENSP00000371502.3:p.Pro1779=
NM_001079846.1:c.5337G=	NP_001073315.1:p.Pro1779=
NM_004380.2:c.5451G=	NP_004371.2:p.Pro1817=
XM_005255124.3:c.5406G=	XP_005255181.1:p.Pro1802=
XM_005255125.3:c.5034G=	XP_005255182.1:p.Pro1678=
XM_006720848.2:c.5190G=	XP_006720911.1:p.Pro1730=
XM_011522380.1:c.5397G=	XP_011520682.1:p.Pro1799=
XM_011522381.1:c.4698G=	XP_011520683.1:p.Pro1566=
XM_005255124.4:c.5406G=	XP_005255181.1:p.Pro1802=
XM_005255125.4:c.5034G=	XP_005255182.1:p.Pro1678=
XM_006720848.3:c.5190G=	XP_006720911.1:p.Pro1730=
XM_011522381.2:c.4698G=	XP_011520683.1:p.Pro1566=
XM_017022944.1:c.5445G=	XP_016878433.1:p.Pro1815=
NM_004380.3:c.5451G= MANE Select	NP_004371.2:p.Pro1817=