Canonical Allele Identifier: CA2202936599

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736701G= , CM000678.2:g.3736701G=	GRCh38
NC_000016.9:g.3786702G= , CM000678.1:g.3786702G=	GRCh37
NC_000016.8:g.3726703G=	NCBI36
NG_009873.1:g.148420C=
NG_009873.2:g.149013C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4509C= MANE Select	ENSP00000262367.5:p.Tyr1503=
ENST00000262367.9:c.4509C=	ENSP00000262367.5:p.Tyr1503=
ENST00000382070.7:c.4395C=	ENSP00000371502.3:p.Tyr1465=
ENST00000570939.2:c.3144C=	ENSP00000461002.2:p.Tyr1048=
ENST00000571763.5:n.299C=
ENST00000574740.1:n.330C=
ENST00000576720.1:n.3332C=
NM_001079846.1:c.4395C=	NP_001073315.1:p.Tyr1465=
NM_004380.2:c.4509C=	NP_004371.2:p.Tyr1503=
XM_005255124.3:c.4464C=	XP_005255181.1:p.Tyr1488=
XM_005255125.3:c.4092C=	XP_005255182.1:p.Tyr1364=
XM_006720848.2:c.4248C=	XP_006720911.1:p.Tyr1416=
XM_011522380.1:c.4455C=	XP_011520682.1:p.Tyr1485=
XM_011522381.1:c.3756C=	XP_011520683.1:p.Tyr1252=
XM_005255124.4:c.4464C=	XP_005255181.1:p.Tyr1488=
XM_005255125.4:c.4092C=	XP_005255182.1:p.Tyr1364=
XM_006720848.3:c.4248C=	XP_006720911.1:p.Tyr1416=
XM_011522381.2:c.3756C=	XP_011520683.1:p.Tyr1252=
XM_017022944.1:c.4503C=	XP_016878433.1:p.Tyr1501=
NM_004380.3:c.4509C= MANE Select	NP_004371.2:p.Tyr1503=