Canonical Allele Identifier: CA2202916153

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728997G= , CM000678.2:g.3728997G=	GRCh38
NC_000016.9:g.3778998G= , CM000678.1:g.3778998G=	GRCh37
NC_000016.8:g.3718999G=	NCBI36
NG_009873.1:g.156124C=
NG_009873.2:g.156717C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6050C= MANE Select	ENSP00000262367.5:p.Pro2017=
ENST00000262367.9:c.6050C=	ENSP00000262367.5:p.Pro2017=
ENST00000382070.7:c.5936C=	ENSP00000371502.3:p.Pro1979=
NM_001079846.1:c.5936C=	NP_001073315.1:p.Pro1979=
NM_004380.2:c.6050C=	NP_004371.2:p.Pro2017=
XM_005255124.3:c.6005C=	XP_005255181.1:p.Pro2002=
XM_005255125.3:c.5633C=	XP_005255182.1:p.Pro1878=
XM_006720848.2:c.5789C=	XP_006720911.1:p.Pro1930=
XM_011522380.1:c.5996C=	XP_011520682.1:p.Pro1999=
XM_011522381.1:c.5297C=	XP_011520683.1:p.Pro1766=
XM_005255124.4:c.6005C=	XP_005255181.1:p.Pro2002=
XM_005255125.4:c.5633C=	XP_005255182.1:p.Pro1878=
XM_006720848.3:c.5789C=	XP_006720911.1:p.Pro1930=
XM_011522381.2:c.5297C=	XP_011520683.1:p.Pro1766=
XM_017022944.1:c.6044C=	XP_016878433.1:p.Pro2015=
NM_004380.3:c.6050C= MANE Select	NP_004371.2:p.Pro2017=