Canonical Allele Identifier: CA2202916238

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729120T= , CM000678.2:g.3729120T=	GRCh38
NC_000016.9:g.3779121T= , CM000678.1:g.3779121T=	GRCh37
NC_000016.8:g.3719122T=	NCBI36
NG_009873.1:g.156001A=
NG_009873.2:g.156594A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5927A= MANE Select	ENSP00000262367.5:p.Asn1976=
ENST00000262367.9:c.5927A=	ENSP00000262367.5:p.Asn1976=
ENST00000382070.7:c.5813A=	ENSP00000371502.3:p.Asn1938=
NM_001079846.1:c.5813A=	NP_001073315.1:p.Asn1938=
NM_004380.2:c.5927A=	NP_004371.2:p.Asn1976=
XM_005255124.3:c.5882A=	XP_005255181.1:p.Asn1961=
XM_005255125.3:c.5510A=	XP_005255182.1:p.Asn1837=
XM_006720848.2:c.5666A=	XP_006720911.1:p.Asn1889=
XM_011522380.1:c.5873A=	XP_011520682.1:p.Asn1958=
XM_011522381.1:c.5174A=	XP_011520683.1:p.Asn1725=
XM_005255124.4:c.5882A=	XP_005255181.1:p.Asn1961=
XM_005255125.4:c.5510A=	XP_005255182.1:p.Asn1837=
XM_006720848.3:c.5666A=	XP_006720911.1:p.Asn1889=
XM_011522381.2:c.5174A=	XP_011520683.1:p.Asn1725=
XM_017022944.1:c.5921A=	XP_016878433.1:p.Asn1974=
NM_004380.3:c.5927A= MANE Select	NP_004371.2:p.Asn1976=