Canonical Allele Identifier: CA2202953629

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3792003G= , CM000678.2:g.3792003G=	GRCh38
NC_000016.9:g.3842004G= , CM000678.1:g.3842004G=	GRCh37
NC_000016.8:g.3782005G=	NCBI36
NG_009873.1:g.93118C=
NG_009873.2:g.93711C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.1308C= MANE Select	ENSP00000262367.5:p.Ala436=
ENST00000262367.9:c.1308C=	ENSP00000262367.5:p.Ala436=
ENST00000382070.7:c.1216+1383C=	ENSP00000371502.3:n.1216+1383C=
NM_001079846.1:c.1216+1383C=	NP_001073315.1:n.1216+1383C=
NM_004380.2:c.1308C=	NP_004371.2:p.Ala436=
XM_005255124.3:c.1308C=	XP_005255181.1:p.Ala436=
XM_005255125.3:c.1308C=	XP_005255182.1:p.Ala436=
XM_006720848.2:c.1308C=	XP_006720911.1:p.Ala436=
XM_011522380.1:c.1254C=	XP_011520682.1:p.Ala418=
XM_011522381.1:c.555C=	XP_011520683.1:p.Ala185=
XM_011522382.1:c.1308C=	XP_011520684.1:p.Ala436=
XM_005255124.4:c.1308C=	XP_005255181.1:p.Ala436=
XM_005255125.4:c.1308C=	XP_005255182.1:p.Ala436=
XM_006720848.3:c.1308C=	XP_006720911.1:p.Ala436=
XM_011522381.2:c.555C=	XP_011520683.1:p.Ala185=
XM_011522382.3:c.1308C=	XP_011520684.1:p.Ala436=
XM_017022944.1:c.1308C=	XP_016878433.1:p.Ala436=
NM_004380.3:c.1308C= MANE Select	NP_004371.2:p.Ala436=