Canonical Allele Identifier: CA2202916143

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728975C= , CM000678.2:g.3728975C=	GRCh38
NC_000016.9:g.3778976C= , CM000678.1:g.3778976C=	GRCh37
NC_000016.8:g.3718977C=	NCBI36
NG_009873.1:g.156146G=
NG_009873.2:g.156739G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6072G= MANE Select	ENSP00000262367.5:p.Ala2024=
ENST00000262367.9:c.6072G=	ENSP00000262367.5:p.Ala2024=
ENST00000382070.7:c.5958G=	ENSP00000371502.3:p.Ala1986=
NM_001079846.1:c.5958G=	NP_001073315.1:p.Ala1986=
NM_004380.2:c.6072G=	NP_004371.2:p.Ala2024=
XM_005255124.3:c.6027G=	XP_005255181.1:p.Ala2009=
XM_005255125.3:c.5655G=	XP_005255182.1:p.Ala1885=
XM_006720848.2:c.5811G=	XP_006720911.1:p.Ala1937=
XM_011522380.1:c.6018G=	XP_011520682.1:p.Ala2006=
XM_011522381.1:c.5319G=	XP_011520683.1:p.Ala1773=
XM_005255124.4:c.6027G=	XP_005255181.1:p.Ala2009=
XM_005255125.4:c.5655G=	XP_005255182.1:p.Ala1885=
XM_006720848.3:c.5811G=	XP_006720911.1:p.Ala1937=
XM_011522381.2:c.5319G=	XP_011520683.1:p.Ala1773=
XM_017022944.1:c.6066G=	XP_016878433.1:p.Ala2022=
NM_004380.3:c.6072G= MANE Select	NP_004371.2:p.Ala2024=