Canonical Allele Identifier: CA2202928415

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727943C= , CM000678.2:g.3727943C=	GRCh38
NC_000016.9:g.3777944C= , CM000678.1:g.3777944C=	GRCh37
NC_000016.8:g.3717945C=	NCBI36
NG_009873.1:g.157178G=
NG_009873.2:g.157771G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7104G= MANE Select	ENSP00000262367.5:p.Gln2368=
ENST00000262367.9:c.7104G=	ENSP00000262367.5:p.Gln2368=
ENST00000382070.7:c.6990G=	ENSP00000371502.3:p.Gln2330=
NM_001079846.1:c.6990G=	NP_001073315.1:p.Gln2330=
NM_004380.2:c.7104G=	NP_004371.2:p.Gln2368=
XM_005255124.3:c.7059G=	XP_005255181.1:p.Gln2353=
XM_005255125.3:c.6687G=	XP_005255182.1:p.Gln2229=
XM_006720848.2:c.6843G=	XP_006720911.1:p.Gln2281=
XM_011522380.1:c.7050G=	XP_011520682.1:p.Gln2350=
XM_011522381.1:c.6351G=	XP_011520683.1:p.Gln2117=
XM_005255124.4:c.7059G=	XP_005255181.1:p.Gln2353=
XM_005255125.4:c.6687G=	XP_005255182.1:p.Gln2229=
XM_006720848.3:c.6843G=	XP_006720911.1:p.Gln2281=
XM_011522381.2:c.6351G=	XP_011520683.1:p.Gln2117=
XM_017022944.1:c.7098G=	XP_016878433.1:p.Gln2366=
NM_004380.3:c.7104G= MANE Select	NP_004371.2:p.Gln2368=