Canonical Allele Identifier: CA2202939784

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3739582T= , CM000678.2:g.3739582T=	GRCh38
NC_000016.9:g.3789583T= , CM000678.1:g.3789583T=	GRCh37
NC_000016.8:g.3729584T=	NCBI36
NG_009873.1:g.145539A=
NG_009873.2:g.146132A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.4276A= MANE Select	ENSP00000262367.5:p.Thr1426=
ENST00000262367.9:c.4276A=	ENSP00000262367.5:p.Thr1426=
ENST00000382070.7:c.4162A=	ENSP00000371502.3:p.Thr1388=
ENST00000570939.2:c.2911A=	ENSP00000461002.2:p.Thr971=
ENST00000573517.6:c.582A=
ENST00000574740.1:n.215+817A=
ENST00000576720.1:n.3213A=
NM_001079846.1:c.4162A=	NP_001073315.1:p.Thr1388=
NM_004380.2:c.4276A=	NP_004371.2:p.Thr1426=
XM_005255124.3:c.4231A=	XP_005255181.1:p.Thr1411=
XM_005255125.3:c.3859A=	XP_005255182.1:p.Thr1287=
XM_006720848.2:c.4133+817A=	XP_006720911.1:n.4133+817A=
XM_011522380.1:c.4222A=	XP_011520682.1:p.Thr1408=
XM_011522381.1:c.3523A=	XP_011520683.1:p.Thr1175=
XM_005255124.4:c.4231A=	XP_005255181.1:p.Thr1411=
XM_005255125.4:c.3859A=	XP_005255182.1:p.Thr1287=
XM_006720848.3:c.4133+817A=	XP_006720911.1:n.4133+817A=
XM_011522381.2:c.3523A=	XP_011520683.1:p.Thr1175=
XM_017022944.1:c.4270A=	XP_016878433.1:p.Thr1424=
NM_004380.3:c.4276A= MANE Select	NP_004371.2:p.Thr1426=