Canonical Allele Identifier: CA2202954944

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3793414C= , CM000678.2:g.3793414C=	GRCh38
NC_000016.9:g.3843415C= , CM000678.1:g.3843415C=	GRCh37
NC_000016.8:g.3783416C=	NCBI36
NG_009873.1:g.91707G=
NG_009873.2:g.92300G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.1188G= MANE Select	ENSP00000262367.5:p.Thr396=
ENST00000262367.9:c.1188G=	ENSP00000262367.5:p.Thr396=
ENST00000382070.7:c.1188G=	ENSP00000371502.3:p.Thr396=
NM_001079846.1:c.1188G=	NP_001073315.1:p.Thr396=
NM_004380.2:c.1188G=	NP_004371.2:p.Thr396=
XM_005255124.3:c.1188G=	XP_005255181.1:p.Thr396=
XM_005255125.3:c.1188G=	XP_005255182.1:p.Thr396=
XM_006720848.2:c.1188G=	XP_006720911.1:p.Thr396=
XM_011522380.1:c.1134G=	XP_011520682.1:p.Thr378=
XM_011522381.1:c.435G=	XP_011520683.1:p.Thr145=
XM_011522382.1:c.1188G=	XP_011520684.1:p.Thr396=
XM_005255124.4:c.1188G=	XP_005255181.1:p.Thr396=
XM_005255125.4:c.1188G=	XP_005255182.1:p.Thr396=
XM_006720848.3:c.1188G=	XP_006720911.1:p.Thr396=
XM_011522381.2:c.435G=	XP_011520683.1:p.Thr145=
XM_011522382.3:c.1188G=	XP_011520684.1:p.Thr396=
XM_017022944.1:c.1188G=	XP_016878433.1:p.Thr396=
NM_004380.3:c.1188G= MANE Select	NP_004371.2:p.Thr396=