Canonical Allele Identifier: CA2202950996

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3770896G= , CM000678.2:g.3770896G=	GRCh38
NC_000016.9:g.3820897G= , CM000678.1:g.3820897G=	GRCh37
NC_000016.8:g.3760898G=	NCBI36
NG_009873.1:g.114225C=
NG_009873.2:g.114818C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2554C= MANE Select	ENSP00000262367.5:p.Pro852=
ENST00000262367.9:c.2554C=	ENSP00000262367.5:p.Pro852=
ENST00000382070.7:c.2440C=	ENSP00000371502.3:p.Pro814=
ENST00000570939.2:c.1159C=	ENSP00000461002.2:p.Pro387=
NM_001079846.1:c.2440C=	NP_001073315.1:p.Pro814=
NM_004380.2:c.2554C=	NP_004371.2:p.Pro852=
XM_005255124.3:c.2509C=	XP_005255181.1:p.Pro837=
XM_005255125.3:c.2464-1543C=	XP_005255182.1:n.2464-1543C=
XM_006720848.2:c.2554C=	XP_006720911.1:p.Pro852=
XM_011522380.1:c.2500C=	XP_011520682.1:p.Pro834=
XM_011522381.1:c.1801C=	XP_011520683.1:p.Pro601=
XM_011522382.1:c.2554C=	XP_011520684.1:p.Pro852=
XM_005255124.4:c.2509C=	XP_005255181.1:p.Pro837=
XM_005255125.4:c.2464-1543C=	XP_005255182.1:n.2464-1543C=
XM_006720848.3:c.2554C=	XP_006720911.1:p.Pro852=
XM_011522381.2:c.1801C=	XP_011520683.1:p.Pro601=
XM_011522382.3:c.2554C=	XP_011520684.1:p.Pro852=
XM_017022944.1:c.2548C=	XP_016878433.1:p.Pro850=
NM_004380.3:c.2554C= MANE Select	NP_004371.2:p.Pro852=