Canonical Allele Identifier: CA2202928451

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728033G= , CM000678.2:g.3728033G=	GRCh38
NC_000016.9:g.3778034G= , CM000678.1:g.3778034G=	GRCh37
NC_000016.8:g.3718035G=	NCBI36
NG_009873.1:g.157088C=
NG_009873.2:g.157681C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7014C= MANE Select	ENSP00000262367.5:p.Ser2338=
ENST00000262367.9:c.7014C=	ENSP00000262367.5:p.Ser2338=
ENST00000382070.7:c.6900C=	ENSP00000371502.3:p.Ser2300=
NM_001079846.1:c.6900C=	NP_001073315.1:p.Ser2300=
NM_004380.2:c.7014C=	NP_004371.2:p.Ser2338=
XM_005255124.3:c.6969C=	XP_005255181.1:p.Ser2323=
XM_005255125.3:c.6597C=	XP_005255182.1:p.Ser2199=
XM_006720848.2:c.6753C=	XP_006720911.1:p.Ser2251=
XM_011522380.1:c.6960C=	XP_011520682.1:p.Ser2320=
XM_011522381.1:c.6261C=	XP_011520683.1:p.Ser2087=
XM_005255124.4:c.6969C=	XP_005255181.1:p.Ser2323=
XM_005255125.4:c.6597C=	XP_005255182.1:p.Ser2199=
XM_006720848.3:c.6753C=	XP_006720911.1:p.Ser2251=
XM_011522381.2:c.6261C=	XP_011520683.1:p.Ser2087=
XM_017022944.1:c.7008C=	XP_016878433.1:p.Ser2336=
NM_004380.3:c.7014C= MANE Select	NP_004371.2:p.Ser2338=