Canonical Allele Identifier: CA2202958651

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3778027T= , CM000678.2:g.3778027T=	GRCh38
NC_000016.9:g.3828028T= , CM000678.1:g.3828028T=	GRCh37
NC_000016.8:g.3768029T=	NCBI36
NG_009873.1:g.107094A=
NG_009873.2:g.107687A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2097A= MANE Select	ENSP00000262367.5:p.Gln699=
ENST00000262367.9:c.2097A=	ENSP00000262367.5:p.Gln699=
ENST00000382070.7:c.1983A=	ENSP00000371502.3:p.Gln661=
ENST00000570939.2:c.702A=	ENSP00000461002.2:p.Gln234=
ENST00000571826.5:c.146A=
ENST00000572134.1:c.410A=
ENST00000634839.1:n.259A=
NM_001079846.1:c.1983A=	NP_001073315.1:p.Gln661=
NM_004380.2:c.2097A=	NP_004371.2:p.Gln699=
XM_005255124.3:c.2097A=	XP_005255181.1:p.Gln699=
XM_005255125.3:c.2097A=	XP_005255182.1:p.Gln699=
XM_006720848.2:c.2097A=	XP_006720911.1:p.Gln699=
XM_011522380.1:c.2043A=	XP_011520682.1:p.Gln681=
XM_011522381.1:c.1344A=	XP_011520683.1:p.Gln448=
XM_011522382.1:c.2097A=	XP_011520684.1:p.Gln699=
XM_005255124.4:c.2097A=	XP_005255181.1:p.Gln699=
XM_005255125.4:c.2097A=	XP_005255182.1:p.Gln699=
XM_006720848.3:c.2097A=	XP_006720911.1:p.Gln699=
XM_011522381.2:c.1344A=	XP_011520683.1:p.Gln448=
XM_011522382.3:c.2097A=	XP_011520684.1:p.Gln699=
XM_017022944.1:c.2097A=	XP_016878433.1:p.Gln699=
NM_004380.3:c.2097A= MANE Select	NP_004371.2:p.Gln699=