Canonical Allele Identifier: CA2202928364

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727839G= , CM000678.2:g.3727839G=	GRCh38
NC_000016.9:g.3777840G= , CM000678.1:g.3777840G=	GRCh37
NC_000016.8:g.3717841G=	NCBI36
NG_009873.1:g.157282C=
NG_009873.2:g.157875C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7208C= MANE Select	ENSP00000262367.5:p.Pro2403=
ENST00000262367.9:c.7208C=	ENSP00000262367.5:p.Pro2403=
ENST00000382070.7:c.7094C=	ENSP00000371502.3:p.Pro2365=
NM_001079846.1:c.7094C=	NP_001073315.1:p.Pro2365=
NM_004380.2:c.7208C=	NP_004371.2:p.Pro2403=
XM_005255124.3:c.7163C=	XP_005255181.1:p.Pro2388=
XM_005255125.3:c.6791C=	XP_005255182.1:p.Pro2264=
XM_006720848.2:c.6947C=	XP_006720911.1:p.Pro2316=
XM_011522380.1:c.7154C=	XP_011520682.1:p.Pro2385=
XM_011522381.1:c.6455C=	XP_011520683.1:p.Pro2152=
XM_005255124.4:c.7163C=	XP_005255181.1:p.Pro2388=
XM_005255125.4:c.6791C=	XP_005255182.1:p.Pro2264=
XM_006720848.3:c.6947C=	XP_006720911.1:p.Pro2316=
XM_011522381.2:c.6455C=	XP_011520683.1:p.Pro2152=
XM_017022944.1:c.7202C=	XP_016878433.1:p.Pro2401=
NM_004380.3:c.7208C= MANE Select	NP_004371.2:p.Pro2403=