Canonical Allele Identifier: CA2202928319

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727745C= , CM000678.2:g.3727745C=	GRCh38
NC_000016.9:g.3777746C= , CM000678.1:g.3777746C=	GRCh37
NC_000016.8:g.3717747C=	NCBI36
NG_009873.1:g.157376G=
NG_009873.2:g.157969G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7302G= MANE Select	ENSP00000262367.5:p.Thr2434=
ENST00000262367.9:c.7302G=	ENSP00000262367.5:p.Thr2434=
ENST00000382070.7:c.7188G=	ENSP00000371502.3:p.Thr2396=
NM_001079846.1:c.7188G=	NP_001073315.1:p.Thr2396=
NM_004380.2:c.7302G=	NP_004371.2:p.Thr2434=
XM_005255124.3:c.7257G=	XP_005255181.1:p.Thr2419=
XM_005255125.3:c.6885G=	XP_005255182.1:p.Thr2295=
XM_006720848.2:c.7041G=	XP_006720911.1:p.Thr2347=
XM_011522380.1:c.7248G=	XP_011520682.1:p.Thr2416=
XM_011522381.1:c.6549G=	XP_011520683.1:p.Thr2183=
XM_005255124.4:c.7257G=	XP_005255181.1:p.Thr2419=
XM_005255125.4:c.6885G=	XP_005255182.1:p.Thr2295=
XM_006720848.3:c.7041G=	XP_006720911.1:p.Thr2347=
XM_011522381.2:c.6549G=	XP_011520683.1:p.Thr2183=
XM_017022944.1:c.7296G=	XP_016878433.1:p.Thr2432=
NM_004380.3:c.7302G= MANE Select	NP_004371.2:p.Thr2434=