Canonical Allele Identifier: CA2202916429

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729495C= , CM000678.2:g.3729495C=	GRCh38
NC_000016.9:g.3779496C= , CM000678.1:g.3779496C=	GRCh37
NC_000016.8:g.3719497C=	NCBI36
NG_009873.1:g.155626G=
NG_009873.2:g.156219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5552G= MANE Select	ENSP00000262367.5:p.Arg1851=
ENST00000262367.9:c.5552G=	ENSP00000262367.5:p.Arg1851=
ENST00000382070.7:c.5438G=	ENSP00000371502.3:p.Arg1813=
NM_001079846.1:c.5438G=	NP_001073315.1:p.Arg1813=
NM_004380.2:c.5552G=	NP_004371.2:p.Arg1851=
XM_005255124.3:c.5507G=	XP_005255181.1:p.Arg1836=
XM_005255125.3:c.5135G=	XP_005255182.1:p.Arg1712=
XM_006720848.2:c.5291G=	XP_006720911.1:p.Arg1764=
XM_011522380.1:c.5498G=	XP_011520682.1:p.Arg1833=
XM_011522381.1:c.4799G=	XP_011520683.1:p.Arg1600=
XM_005255124.4:c.5507G=	XP_005255181.1:p.Arg1836=
XM_005255125.4:c.5135G=	XP_005255182.1:p.Arg1712=
XM_006720848.3:c.5291G=	XP_006720911.1:p.Arg1764=
XM_011522381.2:c.4799G=	XP_011520683.1:p.Arg1600=
XM_017022944.1:c.5546G=	XP_016878433.1:p.Arg1849=
NM_004380.3:c.5552G= MANE Select	NP_004371.2:p.Arg1851=