Canonical Allele Identifier: CA2202916099

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728887G= , CM000678.2:g.3728887G=	GRCh38
NC_000016.9:g.3778888G= , CM000678.1:g.3778888G=	GRCh37
NC_000016.8:g.3718889G=	NCBI36
NG_009873.1:g.156234C=
NG_009873.2:g.156827C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6160C= MANE Select	ENSP00000262367.5:p.Pro2054=
ENST00000262367.9:c.6160C=	ENSP00000262367.5:p.Pro2054=
ENST00000382070.7:c.6046C=	ENSP00000371502.3:p.Pro2016=
NM_001079846.1:c.6046C=	NP_001073315.1:p.Pro2016=
NM_004380.2:c.6160C=	NP_004371.2:p.Pro2054=
XM_005255124.3:c.6115C=	XP_005255181.1:p.Pro2039=
XM_005255125.3:c.5743C=	XP_005255182.1:p.Pro1915=
XM_006720848.2:c.5899C=	XP_006720911.1:p.Pro1967=
XM_011522380.1:c.6106C=	XP_011520682.1:p.Pro2036=
XM_011522381.1:c.5407C=	XP_011520683.1:p.Pro1803=
XM_005255124.4:c.6115C=	XP_005255181.1:p.Pro2039=
XM_005255125.4:c.5743C=	XP_005255182.1:p.Pro1915=
XM_006720848.3:c.5899C=	XP_006720911.1:p.Pro1967=
XM_011522381.2:c.5407C=	XP_011520683.1:p.Pro1803=
XM_017022944.1:c.6154C=	XP_016878433.1:p.Pro2052=
NM_004380.3:c.6160C= MANE Select	NP_004371.2:p.Pro2054=