Canonical Allele Identifier: CA2202928398

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727909T= , CM000678.2:g.3727909T=	GRCh38
NC_000016.9:g.3777910T= , CM000678.1:g.3777910T=	GRCh37
NC_000016.8:g.3717911T=	NCBI36
NG_009873.1:g.157212A=
NG_009873.2:g.157805A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7138A= MANE Select	ENSP00000262367.5:p.Thr2380=
ENST00000262367.9:c.7138A=	ENSP00000262367.5:p.Thr2380=
ENST00000382070.7:c.7024A=	ENSP00000371502.3:p.Thr2342=
NM_001079846.1:c.7024A=	NP_001073315.1:p.Thr2342=
NM_004380.2:c.7138A=	NP_004371.2:p.Thr2380=
XM_005255124.3:c.7093A=	XP_005255181.1:p.Thr2365=
XM_005255125.3:c.6721A=	XP_005255182.1:p.Thr2241=
XM_006720848.2:c.6877A=	XP_006720911.1:p.Thr2293=
XM_011522380.1:c.7084A=	XP_011520682.1:p.Thr2362=
XM_011522381.1:c.6385A=	XP_011520683.1:p.Thr2129=
XM_005255124.4:c.7093A=	XP_005255181.1:p.Thr2365=
XM_005255125.4:c.6721A=	XP_005255182.1:p.Thr2241=
XM_006720848.3:c.6877A=	XP_006720911.1:p.Thr2293=
XM_011522381.2:c.6385A=	XP_011520683.1:p.Thr2129=
XM_017022944.1:c.7132A=	XP_016878433.1:p.Thr2378=
NM_004380.3:c.7138A= MANE Select	NP_004371.2:p.Thr2380=