Canonical Allele Identifier: CA2202928465

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728064G= , CM000678.2:g.3728064G=	GRCh38
NC_000016.9:g.3778065G= , CM000678.1:g.3778065G=	GRCh37
NC_000016.8:g.3718066G=	NCBI36
NG_009873.1:g.157057C=
NG_009873.2:g.157650C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6983C= MANE Select	ENSP00000262367.5:p.Ser2328=
ENST00000262367.9:c.6983C=	ENSP00000262367.5:p.Ser2328=
ENST00000382070.7:c.6869C=	ENSP00000371502.3:p.Ser2290=
NM_001079846.1:c.6869C=	NP_001073315.1:p.Ser2290=
NM_004380.2:c.6983C=	NP_004371.2:p.Ser2328=
XM_005255124.3:c.6938C=	XP_005255181.1:p.Ser2313=
XM_005255125.3:c.6566C=	XP_005255182.1:p.Ser2189=
XM_006720848.2:c.6722C=	XP_006720911.1:p.Ser2241=
XM_011522380.1:c.6929C=	XP_011520682.1:p.Ser2310=
XM_011522381.1:c.6230C=	XP_011520683.1:p.Ser2077=
XM_005255124.4:c.6938C=	XP_005255181.1:p.Ser2313=
XM_005255125.4:c.6566C=	XP_005255182.1:p.Ser2189=
XM_006720848.3:c.6722C=	XP_006720911.1:p.Ser2241=
XM_011522381.2:c.6230C=	XP_011520683.1:p.Ser2077=
XM_017022944.1:c.6977C=	XP_016878433.1:p.Ser2326=
NM_004380.3:c.6983C= MANE Select	NP_004371.2:p.Ser2328=