Canonical Allele Identifier: CA2202928485

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728114C= , CM000678.2:g.3728114C=	GRCh38
NC_000016.9:g.3778115C= , CM000678.1:g.3778115C=	GRCh37
NC_000016.8:g.3718116C=	NCBI36
NG_009873.1:g.157007G=
NG_009873.2:g.157600G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6933G= MANE Select	ENSP00000262367.5:p.Pro2311=
ENST00000262367.9:c.6933G=	ENSP00000262367.5:p.Pro2311=
ENST00000382070.7:c.6819G=	ENSP00000371502.3:p.Pro2273=
NM_001079846.1:c.6819G=	NP_001073315.1:p.Pro2273=
NM_004380.2:c.6933G=	NP_004371.2:p.Pro2311=
XM_005255124.3:c.6888G=	XP_005255181.1:p.Pro2296=
XM_005255125.3:c.6516G=	XP_005255182.1:p.Pro2172=
XM_006720848.2:c.6672G=	XP_006720911.1:p.Pro2224=
XM_011522380.1:c.6879G=	XP_011520682.1:p.Pro2293=
XM_011522381.1:c.6180G=	XP_011520683.1:p.Pro2060=
XM_005255124.4:c.6888G=	XP_005255181.1:p.Pro2296=
XM_005255125.4:c.6516G=	XP_005255182.1:p.Pro2172=
XM_006720848.3:c.6672G=	XP_006720911.1:p.Pro2224=
XM_011522381.2:c.6180G=	XP_011520683.1:p.Pro2060=
XM_017022944.1:c.6927G=	XP_016878433.1:p.Pro2309=
NM_004380.3:c.6933G= MANE Select	NP_004371.2:p.Pro2311=