Canonical Allele Identifier: CA2202916469

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729611G= , CM000678.2:g.3729611G=	GRCh38
NC_000016.9:g.3779612G= , CM000678.1:g.3779612G=	GRCh37
NC_000016.8:g.3719613G=	NCBI36
NG_009873.1:g.155510C=
NG_009873.2:g.156103C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5436C= MANE Select	ENSP00000262367.5:p.Thr1812=
ENST00000262367.9:c.5436C=	ENSP00000262367.5:p.Thr1812=
ENST00000382070.7:c.5322C=	ENSP00000371502.3:p.Thr1774=
NM_001079846.1:c.5322C=	NP_001073315.1:p.Thr1774=
NM_004380.2:c.5436C=	NP_004371.2:p.Thr1812=
XM_005255124.3:c.5391C=	XP_005255181.1:p.Thr1797=
XM_005255125.3:c.5019C=	XP_005255182.1:p.Thr1673=
XM_006720848.2:c.5175C=	XP_006720911.1:p.Thr1725=
XM_011522380.1:c.5382C=	XP_011520682.1:p.Thr1794=
XM_011522381.1:c.4683C=	XP_011520683.1:p.Thr1561=
XM_005255124.4:c.5391C=	XP_005255181.1:p.Thr1797=
XM_005255125.4:c.5019C=	XP_005255182.1:p.Thr1673=
XM_006720848.3:c.5175C=	XP_006720911.1:p.Thr1725=
XM_011522381.2:c.4683C=	XP_011520683.1:p.Thr1561=
XM_017022944.1:c.5430C=	XP_016878433.1:p.Thr1810=
NM_004380.3:c.5436C= MANE Select	NP_004371.2:p.Thr1812=