Canonical Allele Identifier: CA2202928492

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728130C= , CM000678.2:g.3728130C=	GRCh38
NC_000016.9:g.3778131C= , CM000678.1:g.3778131C=	GRCh37
NC_000016.8:g.3718132C=	NCBI36
NG_009873.1:g.156991G=
NG_009873.2:g.157584G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6917G= MANE Select	ENSP00000262367.5:p.Gly2306=
ENST00000262367.9:c.6917G=	ENSP00000262367.5:p.Gly2306=
ENST00000382070.7:c.6803G=	ENSP00000371502.3:p.Gly2268=
NM_001079846.1:c.6803G=	NP_001073315.1:p.Gly2268=
NM_004380.2:c.6917G=	NP_004371.2:p.Gly2306=
XM_005255124.3:c.6872G=	XP_005255181.1:p.Gly2291=
XM_005255125.3:c.6500G=	XP_005255182.1:p.Gly2167=
XM_006720848.2:c.6656G=	XP_006720911.1:p.Gly2219=
XM_011522380.1:c.6863G=	XP_011520682.1:p.Gly2288=
XM_011522381.1:c.6164G=	XP_011520683.1:p.Gly2055=
XM_005255124.4:c.6872G=	XP_005255181.1:p.Gly2291=
XM_005255125.4:c.6500G=	XP_005255182.1:p.Gly2167=
XM_006720848.3:c.6656G=	XP_006720911.1:p.Gly2219=
XM_011522381.2:c.6164G=	XP_011520683.1:p.Gly2055=
XM_017022944.1:c.6911G=	XP_016878433.1:p.Gly2304=
NM_004380.3:c.6917G= MANE Select	NP_004371.2:p.Gly2306=